Name: detection of intracellular gene expression in live cells of murine, human and porcine origin using fluorescence-labeled nanoparticles
Uploaded: 2015-11-13T14:00:00
Duration: 8 min 14 s
Description: Watch this Scientific Journal Video about Detection of Intracellular Gene Expression in Live Cells of Murine, Human and Porcine Origin Using Fluorescence-labeled Nanoparticles at JoVE.com

We thank Lynette Henkel for her excellent support in performing the flow cytometric analysis. We thank Dr. Don Weldon and Dr. Victor Koong (Temecula, CA) for critical reading of the manuscript and helpful comments. This work was supported by grants from the German Research Foundation, KR-3770-7/1 and KR-3770-9/1 (M. K.), the Deutsche Stiftung f&#252;r Herzforschung, F/37/11 (M. K.), Dr. Rusche Research Grant 2014 from the Deutsche Stiftung f&#252;r Herzforschung and Deutsche Gesellschaft f&#252;r Thorax-, Herz- und Gef&#228;sschirurgie (M.-A. D.), and the Deutsches Zentrum f&#252;r Herz- und Kreislaufforschung S&#228;ule B Projekt, DZHK B 13-050A and DZHK B 14-013SE (M. K.).

1. Preparation of Media, Reagents and Cell Culture Conditions
<ol>
	<li>Human HEK 293 embryonic kidney cells
	<ol>
		<li>Culture HEK 293 cells (CRL-1573, ATCC) in DMEM/Ham&#8217;s F-12 medium supplemented with 5% FCS, L-glutamine (2 mM), and penicillin (100 U/ml)/ streptomycin (100 &#181;g/ml).</li>
		<li>To passage the cells, wash cells once with PBS, add 0.05% Trypsin/EDTA and incubate for 3 min at 37 &#176;C and 5% CO2. Transfer cells into a 15 ml tube, centrifuge for 5 min at 1,200 rpm (300 x g) and transfer approximately 5x105 cells into a fresh T25 culture flask.</li>
	</ol>
	</li>
	<li>Murine embryonic fibroblasts (MEFs)
	<ol>
		<li>Add 1 ml of a 0.1% gelatin solution to individual 6-wells and incubate at room temperature (RT) for 1 hr. Aspirate liquid and store at RT until use.</li>
		<li>Culture MEFs in DMEM supplemented with 10% FCS, L-glutamine (2 mM), L-glucose (4.5 g/l), sodium pyruvate (1 mM), and penicillin (100 U/ml)/streptomycin (100 &#181;g/ml) on gelatin-coated 6-well plates.</li>
		<li>Distribute MEFs into 6-well plates and let them grow until confluence. Add mitomycin (5 &#181;g/ml) for 2.5 hr to arrest cells. Aspirate medium, wash cells twice with complete MEF medium and add 3 ml MEF medium to each 6-well. These cells serve as a feeder-layer for murine and porcine iPS cells.</li>
	</ol>
	</li>
	<li>Culture of murine ES and iPS cells
	<ol>
		<li>To prepare mouse ES culture medium, supplement DMEM medium with 15% FCS, L-glutamine (2 mM), L-glucose (4.5 g/l), MEM non-essential amino acids (1X), &#946;-mercaptoethanol (0.1 mM) and leukemia inhibitory factor (1.000 U/ml).</li>
		<li>Rinse 6-wells with growth-arrested MEFs once with serum-free DMEM, add 2 ml mouse ES medium and murine iPS cells (20% of the cells of a confluent dish). Every day wash cells once with serum-free DMEM and add 2 ml fresh mouse ES medium.</li>
		<li>To passage the cells, wash each well once with serum-free DMEM, add 0.25% Trypsin/EDTA and incubate for 3 min at 37 &#176;C and 5% CO2. Transfer cells into a 15 ml tube, centrifuge for 5 min at 1,200 rpm (300 x g), resuspend cells in 500 &#181;l mouse ES medium and add 100 &#181;l of the suspension to 2 ml mouse ES medium in a fresh 6-well with a MEF feeder-layer.</li>
	</ol>
	</li>
	<li>Culture of pig iPS cells
	<ol>
		<li>To prepare pig iPS medium, supplement DMEM/Ham&#8217;s F-12 medium with 20% knockout serum, L-glutamine (2 mM), MEM non-essential amino acids (1X), &#946;-mercaptoethanol (0.1 mM), and penicillin (100 U/ml)/streptomycin (100 &#181;g/ml). Filter through a 0.22 &#181;M filter and store at 4 &#176;C for 2 to 3 weeks. Upon first use, add bFGF (10 ng/ml final concentration).</li>
		<li>Rinse 6-wells with growth-arrested MEFs once with serum-free DMEM/Ham&#8217;s F-12 and add 1.5 ml pig iPS medium and porcine iPS cells (10% of the cells of a confluent dish). Every day wash cells once with serum-free DMEM/Ham&#8217;s F-12 and add 1.5 ml fresh pig iPS medium.</li>
		<li>To prepare dissociation buffer add 2.5% trypsin, collagenase IV (10 mg/ml), knockout serum (20%) and CaCl2 (1 mM) to Ca2+-free PBS. Wash cells twice with PBS and incubate with dissociation buffer for 5 min at 37 &#176;C and 5% CO2. Transfer cells into a 15 ml tube, centrifuge for 5 min at 1,200 rpm (300 x g).</li>
		<li>Resuspend porcine iPS cells in 500 &#181;l fresh pig iPS medium and add 50 &#181;l of the suspension to 1.5 ml pig iPS medium in a fresh 6-well with a MEF feeder-layer. Every day wash cells once with serum-free DMEM/Ham&#8217;s F-12 and add 1.5 ml fresh pig iPS medium.</li>
	</ol>
	</li>
	<li>Feeder-free culture of human iPS cells
	<ol>
		<li>Thaw the original vial containing the basement membrane preparation at 4 &#176;C and dilute with ice-cold serum-free DMEM/Ham&#8217;s F-12 to 8 mg/ml, aliquot and store at -20 &#176;C until further use.</li>
		<li>Thaw an aliquot of the basement membrane preparation at 4 &#176;C and dilute with ice-cold serum-free DMEM/Ham&#8217;s F12 (90 &#181;g/ml). Pipet 1 ml of this solution into 3 cm culture dishes and swirl gently to ensure that the whole surface is covered. Seal dishes with parafilm and store at 4 &#176;C for up to one week. Prior to the use for cell culture incubate dishes for 30 min at 37 &#176;C or 3 hr at RT to allow polymerization of the basement membrane preparation.</li>
		<li>Aspirate medium from dishes coated with the basement membrane preparation and wash twice with serum-free DMEM/Ham&#8217;s F-12. Add 1.5 ml E8 medium to the culture dish and human iPS cells (10% of the cells of a confluent dish). Every day wash cells once with serum-free DMEM/Ham&#8217;s F-12 and add 1.5 ml fresh E8 medium.</li>
		<li>To passage the cells, rinse dishes twice with PBS and add 1 ml PBS/0.5 mM EDTA. Incubate the dishes for 5 min at RT. Monitor the cells under a microscope. Note: When the colonies start to round up and appear to have holes they are ready for transfer.</li>
		<li>Aspirate the liquid, add 1.5 ml E8 medium and detach cells by gently pipetting up and down. Transfer cells to a 15 ml tube, centrifuge for 5 min at 1,200 rpm (300 x g), resuspend in 500 &#181;l E8 medium and add 50 &#181;l of the suspension to 1.5 ml E8 medium in a fresh culture dish coated with the basement membrane preparation.</li>
	</ol>
	</li>
</ol>
2. Design of Target-sequences Across Species Borders
<ol>
	<li>Select reference human, murine and porcine cDNA sequences of the target genes (GAPDH, NANOG, GDF3) and perform a CLUSTAL multi-sequence alignment analysis. 
	Note: This will indicate the sequences homologous between species.
	<ol>
		<li>Use the following settings for multiple alignment: gap penalty (fixed) 10, gap penalty (varying) 5, transition weighting 0, gap separation penalty range 8, % identity for delay 40, maximum number of iterations to perform 3.</li>
	</ol>
	</li>
	<li>Submit desired target sequences to the manufacturer (see Table of Materials) for probe design and manufacturing. 
	Note: The manufacturer will then confirm compatibility of desired sequence with the technology. If desired sequence is not compatible, the manufacturer will suggest alternative sequences.
	<ol>
		<li>Ensure that homologous regions which can be used as potential capture strand sequences have a length of 27 bp. 
		Note: It is advisable to order several nanoparticles with different capture strands for a selected target gene as only the real cellular experiment will give a definite proof of the functionality of an individual sequence. Therefore, two different sequences for GAPDH and GDF3 were evaluated while three different nanoparticles were tested to evaluate NANOG expression. Their location and the exact sequences have been published elsewhere 17. The manufacturer commercially manufactures the nanoparticles with desired sequences and provides them in lyophilized format.</li>
	</ol>
	</li>
</ol>
3. Reconstitution of Nanoparticles and Addition to Cell Cultures
<ol>
	<li>Store lyophilized nanoparticles upon receipt at 4 &#176;C in the dark.</li>
	<li>Reconstitute nanoparticles by addition of 50 &#181;l double distilled water which gives a final concentration of 100 nM. Once reconstituted store nanoparticles at RT in the dark. Note: Under this condition they are stable for at least one year. Storage of reconstituted samples at 4 &#176;C may adversely affect their stability.</li>
	<li>Pre-dilute the nanoparticle stock solution with PBS to a concentration of 2 (HEK 293 cells) or 8 nM (iPS and ES cells) on the day of application. Note: This concentration is 20-fold higher than the final concentration in the culture dish. In ES cells and iPS cells, 400 pM of nanoparticles induced a fluorescent signal easily detectable under the microscope. For HEK 293 cells, a concentration of 100 pM is sufficient.</li>
	<li>Pipet 12.5 &#181;l of prediluted nanoparticles to a 24-well containing 237.5 &#181;l complete cell culture medium. For wells of different sizes, adjust the volumes accordingly. Swirl the plate carefully to ensure equal distribution of the nanoparticles. Incubate the cells overnight (O/N) at 37 &#176;C and 5% CO2 in a humidified atmosphere.</li>
	<li>The next day analyze cell cultures for gene-specific Cy3 fluorescence with an excitation wavelength of 546 nm (emission 575 &#8211; 640 nm) under a fluorescence microscope. Note: The period required to obtain a sufficiently strong fluorescence may depend on the cell type and the target gene. In these experiments, this was seen between 16 and 20 hr after the application of the probe.</li>
</ol>
4. Identification of Cy3 Positive Cell Populations by Flow Cytometry
<ol>
	<li>Grow HEK 293 or murine ES cells using the conditions specified in section 1.1 or 1.3, respectively. One day prior to the FACS analysis add GAPDH-specific nanoparticles at different concentrations to HEK 293 cells (see Figure 6A) and at 400 pM to murine ES cells. Incubate the cells O/N at 37 &#176;C and 5% CO2 in a humidified atmosphere.</li>
	<li>Analyze cell cultures for gene-specific Cy3-induced fluorescence under a fluorescence microscope.</li>
	<li>Detach HEK 293 cells as specified under point 1.1.2. Centrifuge, transfer into a 1.5 ml tube and resuspend in 200 &#181;l ice-cold PBS/0.5% BSA/2 mM EDTA (FACS buffer). Keep cells dark on ice until flow cytometric analysis.</li>
	<li>Detach murine ES cells as specified under point 1.3.3. Centrifuge, transfer into a 1.5 ml tube and resuspend in 200 &#181;l ice-cold PBS/0.5% BSA/2 mM EDTA. Keep cells dark on ice until flow cytometric analysis.</li>
	<li>Press the cells through a 30 &#181;M filter to prevent cell aggregation and add propidium iodide (2 &#181;g/ml final concentration) 2 min prior to the FACS analysis to exclude dead cells.</li>
	<li>To analyze Cy3-positive cells first set hierarchical gates on the FSC-A/SSC-A subset, the FSC-H/FSC-W-subset and the SSC-H/SSC-W subset. Use the forward and the side scatter to exclude cell debris and cells that are not scattered. Exclude dead cells by their propidium iodide staining displaying PE against PE-Texas Red. Perform the final sort gate on Cy3-PE positive cells (Figure 4).</li>
</ol>

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H.L. has received the nanoparticles from EMD Millipore Corporation free of charge. All other authors have nothing to disclose.

The present work describes the use of fluorescence labeled nanoparticles which allow the reliable evaluation of intracellular gene expression directly in live cells from different mammalian species with diverse histogenetic origin under a fluorescence microscope. This approach has a couple of advantages compared to other published methods. First of all the researcher is not limited with respect to either the target gene or cell type. All antibody based detection methods are restricted to a single epitope. Although fluorescent molecular beacons can also be designed for a broad spectrum of genes, this method requires the dissociation of cells and subsequent nucleofection 15. In contrast, the application of gene-specific nanoparticles does not require any manipulation of the target cell which engulfs the nanoparticles actively by endocytosis. During subsequent passaging the gold particles gradually leave the cells and the culture can be used in downstream experiments.
Nevertheless, the technology also still has some limitations. Some markers are obviously not detectable due to their carbohydrate nature such as SSEA-1 or TRA-1-81 20. At present, a large array of nanoparticles is commercially available. These particles have been pretested for their functionality in cellular experiments. The objective of the present work was to design customized probes which can be used across species borders. When following such an approach or when designing a probe for a novel target gene one has to be aware that the functionality of an in silico predicted probe needs to be thoroughly evaluated in vitro. The NANOG-SF3 probe which showed a 100% homology to the sequence homology did not work at all while NANOG-SF1 with one mismatched base in the murine and porcine sequence produced a nice fluorescence signal. Another question refers to the efficient uptake of the nanoparticles. The particles enter the cells by endocytosis, a process which is influenced by the size of the nanoparticles 21, the cell type and the differentiation status 22 and the cellular capability to perform phago- and macropinocytosis 23. The optimum concentration to obtain a satisfying fluorescence signal has to be tested for each individual application or cell line. To that end, the first experiment should always be the application of the uptake control to evaluate the compatibility of the probes within the cell types and culture conditions before moving on to target-specific detection of gene expression.
A critical point to obtain reliable results when applying this protocol to a novel cell line or cell population is the inclusion of proper controls. The ever fluorescing uptake control will provide a hint which concentrations of nanoparticles will induce a sufficient fluorescent signal in the target cell population. The fluorescence must be evaluated the next day as the signal will fade with time 17. At the same time the scramble control without a counterpart in the eukaryotic genome applied at an identical concentration must induce a negligible background signal. As a third control it is advisable to use a nanoparticle specific for a housekeeping gene (e.g. GAPDH, &#946;-Actin). These nanoparticles serve as a positive control that the approach can be used to detect specific gene expression in the selected target cell population. If these controls turn out satisfactory one can expect to obtain reliable specific fluorescent signals using nanoparticles specific for other target genes. The concentration of the applied nanoparticles may also be critical as they have been shown to down-regulate the target sequence 24. However, this effect requires much higher concentrations ( 5 nM) than the concentrations used in the experiments presented here (400 pM). At this concentration the nanoflares do not affect target gene mRNA or protein levels and concentrations as high as 2 nM do not impair the proliferation of HEK293 and murine ES cells 17. In addition, a whole genome expression analysis did not reveal any significant changes in gene expression 25. Therefore, at concentrations up to 1 nM the nanoflares should not exhibit any important adverse effects.
A very promising application of this technology is the possibility to label any given cell population which is marked by a specific gene. Recently, gene-specific nanoparticles have successfully been used to selectively stain live ventricular myocytes 26, subpopulations of melanoma cells 27, monocytes 28 and cerebellar cell cultures 29. Such fluorescence-marked cell populations can be sorted and purified by flow cytometry as live cells. In the field of oncology it is imaginable to isolate live metastatic tumor cells in animal models based on their expression of CEA, most valuable for the search of potential metastasis promoting genes or target structures. We have recently shown that truly reprogrammed murine iPS colonies can be identified in situ with Nanog-specific nanoparticles based on the detected fluorescence intensity 17. Therefore, the identification of truly reprogrammed iPS colonies could be performed on high throughput platforms, which use robotic fluorescence detection and picking devices to identify the most promising colonies. This technology appears to be suitable in many research areas to select specific cellular subpopulations and it seems possible to apply the nanoparticles in high throughput platforms. In conclusion, this protocol represents a novel approach using fluorescence labeled nanoparticles which allows the detection of intracellular gene expression directly in live cells. This technology may be a valuable tool to purify, expand and further characterize rare cellular subpopulations in many research areas.

In 2006, a novel approach was described to reprogram somatic cells into a pluripotent state. After prescreening of an array of potential reprogramming factors murine fibroblasts could be successfully converted to so-called induced pluripotent stem cells (iPS) by retroviral transduction and overexpression of four transcription factors (Oct4, Sox2, Klf4, c-Myc) 1. Subsequently this technique has effectively been reproduced using somatic cells of different mammalian species including humans 2, monkeys 3, rats 4, dogs 5, sheep 6 and pigs 7. In addition, modified protocols omitting or replacing the potentially oncogenic transcription factor c-MYC have been published 8, 9.
Regardless of the initial reprogramming approach the true pluripotency of growing colonies has to be confirmed, a laborious and time-consuming task. A major drawback of the majority of these analyses is that they cannot be performed on live cells. Established pluripotency factors such as OCT4, SOX2, NANOG or REX1 represent transcription factors located in the nucleus and their detection requires fixation of the cells prior to immunohistochemistry or cell lysis for RT-PCR analysis 10 - 12. Thereafter, these cells are lost for future experiments requiring replicate cultures of each colony.
Thus, a technology to analyze pluripotency on live cells is highly desirable. Several approaches can indeed be performed directly on live cells using antibodies directed against membrane-based antigens (e.g. TRA-1-60, SSEA4) 12, fluorescent reported dyes to detect alkaline phosphatase 13 or small molecules which specifically label embryonic stem (ES) and iPS cells 14. However, the antibodies might nevertheless adversely affect the cells and each method is restricted to a single pluripotency marker. Finally, fluorescent molecular beacons, dual-antisense oligonucleotides with hairpin structures, which allow live staining of cells, have been described 15. Although this approach may be applied to many genes, the technique requires nucleofection of a single cell suspension, which is not applicable to growing iPS colonies.
A couple of years ago gene-specific nanoparticles have been described to analyze survivin expression in human SKBR3 breast cancer cells 16. This manuscript describes a novel innovative approach to detecting pluripotency markers in live ES and iPS cells through the use of gold nanoparticle conjugates. These nanoparticles consist of a central gold particle with a coupled capture strand carrying the complementary RNA sequence and a Cy3-labeled reporter strand. The fluorescent signal of the reporter strand is quenched by the central gold particle. In addition, appropriate nanoparticles serve as negative and positive controls, respectively (Figure 1). For an application the nanoparticles are simply added to the culture medium (Figure 2) and enter the cells via endocytosis (Figure 3). If the target RNA is expressed it displaces the reporter strand which then emits a fluorescent signal. This method does not require manipulation of the target cell and the expression of the target gene can be monitored optically under a fluorescence microscope directly in live cells. Furthermore, the technology can be applied to any desired target gene across species in the case of iPS cells and thus may be employed in many different research areas. Finally, flow cytometric analyses allow the identification and enrichment of Cy3 positive cells.

<table border="0">
	<tbody>
		<tr>
			<td>DMEM/Ham&#39;s F12 medium with stable glutamine</td>
			<td>Biochrome GmbH</td>
			<td>FG4815</td>
			<td></td>
		</tr>
		<tr>
			<td>Fetal calf serum</td>
			<td>Life Technologies</td>
			<td>SV30160.03</td>
			<td></td>
		</tr>
		<tr>
			<td>Penicillin/Streptomycin (100x)</td>
			<td>Millipore</td>
			<td>A2213</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium pyruvate (100x)</td>
			<td>Life Technologies</td>
			<td>11360-039</td>
			<td></td>
		</tr>
		<tr>
			<td>DMEM high glucose with stable glutamine</td>
			<td>Biochrome GmbH</td>
			<td>FG0435</td>
			<td></td>
		</tr>
		<tr>
			<td>Mitomycin C</td>
			<td>Roche</td>
			<td>10 107 409 001</td>
			<td>prevents cell division of MEFs</td>
		</tr>
		<tr>
			<td>MEM non-essential amino acids (100x)</td>
			<td>Life Technologies</td>
			<td>11140-050</td>
			<td></td>
		</tr>
		<tr>
			<td>b-Mercaptoethanol</td>
			<td>Sigma</td>
			<td>M3148</td>
			<td></td>
		</tr>
		<tr>
			<td>Leukemia inhibitory factor (107 U/ml)</td>
			<td>Millipore</td>
			<td>ESG1107</td>
			<td>growth factor for murine ES and iPS cells, prevents differentiation</td>
		</tr>
		<tr>
			<td>0.25% Trypsin/EDTA (1x)</td>
			<td>Life Technologies</td>
			<td>25200-056</td>
			<td>detaches adherent cell cultures</td>
		</tr>
		<tr>
			<td>Knockout serum</td>
			<td>Invitrogen</td>
			<td>10828-028</td>
			<td>supplement for human and porcine iPS cell culture</td>
		</tr>
		<tr>
			<td>bFGF</td>
			<td>Peprotech</td>
			<td>100-18B</td>
			<td>growth factor for human and porcine iPS cells</td>
		</tr>
		<tr>
			<td>Collagenase IV</td>
			<td>Worthington</td>
			<td>LS004188</td>
			<td>dissociation of pig iPS cells</td>
		</tr>
		<tr>
			<td>Matrigel</td>
			<td>Corning</td>
			<td>354277</td>
			<td>effective surface for feeder-free culture of human iPS cells, referred to as basement preparation membrane in the manuscript</td>
		</tr>
		<tr>
			<td>E8 medium</td>
			<td>Stem Cell Technologies</td>
			<td>05940</td>
			<td>defined medium for feeder-free culture of human iPS cells on Matrigel</td>
		</tr>
		<tr>
			<td>EDTA 0.5 M</td>
			<td>Invitrogen</td>
			<td>15575-038</td>
			<td></td>
		</tr>
		<tr>
			<td>SmartFlare Probes</td>
			<td>EMD Millipore Corporation</td>
			<td>customized item</td>
			<td>detection of intracellular gene expression in live cells, referred to as nanoparticles in the manuscript</td>
		</tr>
		<tr>
			<td>Fluorescence microscope</td>
			<td>Zeiss</td>
			<td>Axiovert 200M</td>
			<td></td>
		</tr>
		<tr>
			<td>HeraCell 150i CO2 Incubator</td>
			<td>Thermo Scientific</td>
			<td>51026282</td>
			<td></td>
		</tr>
		<tr>
			<td>Gelatine (from porcine skin)</td>
			<td>Sigma</td>
			<td>G6144</td>
			<td>enhances attachment of MEFs to surface</td>
		</tr>
		<tr>
			<td>Propidium iodide (1 mg/ml)</td>
			<td>Sigma</td>
			<td>P4864</td>
			<td>labels dead cells in flow cytometric analyses</td>
		</tr>
		<tr>
			<td>BD FACS Aria Illu</td>
			<td>Becton Dickinson</td>
			<td>A4544</td>
			<td>referred to as device 1 in Figure 4</td>
		</tr>
		<tr>
			<td>Navios</td>
			<td>Beckman Coulter</td>
			<td>775213</td>
			<td>referred to as device 2 in Figure 4</td>
		</tr>
		<tr>
			<td>FloJo vX 10.0.7r2</td>
			<td>Treestar</td>
			<td></td>
			<td>software for analysis of flow cytometry data</td>
		</tr>
	</tbody>
</table>

detection of intracellular gene expression in live cells of murine, human and porcine origin using fluorescence-labeled nanoparticles

The reprogramming of somatic cells to induced pluripotent stem cells (iPS) has successfully been performed in different mammalian species including mouse, rat, human, pig and others. The verification of iPS clones mainly relies on the detection of the endogenous expression of different pluripotency genes. These genes mostly represent transcription factors which are located in the cell nucleus. Traditionally, the proof of their endogenous expression is supplied by immunohistochemical staining after fixation of the cells. This approach requires replicate cultures of each clone at this early stage to preserve validated clones for further experiments. The present protocol describes an approach with gene-specific nanoparticles which allows the evaluation of intracellular gene expression directly in live cells by fluorescence. The nanoparticles consist of a central gold particle coupled to a capture strand carrying a sequence complementary to the target mRNA as well as a quenched reporter strand. These nanoparticles are actively endocytosed and the target mRNA displaces the reporter strand which then start to fluoresce. Therefore, specific target gene expression can be detected directly under the microscope. In addition, the emitted fluorescence allows the identification, isolation and enrichment of cells expressing a specific gene by flow cytometry. This method can be applied directly to live cells in culture without any manipulation of the target cells.

In a first attempt to verify and establish the intracellular detection of specific gene expression in live cells using nanoparticles we decided to conduct pilot experiments using a constitutively expressed house-keeping gene (GAPDH) in human HEK 293 cells. The concentration of nanoparticles used in these experiments was chosen according to the recommendation of the manufacturer. The addition of a GAPDH-specific probe to the culture medium at a 100 pM final concentration induced a clear-cut Cy3-fluorescence in these cells which was visible under a fluorescence microscope after O/N incubation (Figure 5A). Two controls were included in these experiments to substantiate the result. One control comprises of a so-called &#8220;scramble&#8221; nanoparticle where the reporter strand does not have a matching sequence in mammalian or eukaryotic cells. The &#8220;scramble&#8221; nanoparticle determines the unspecific background fluorescence due to possible probe degradation or incomplete quenching of the fluorescence. The addition of the scramble probe produced an only marginal fluorescent signal, which is negligible (Figure 5B). A permanently fluorescing &#8220;uptake&#8221; control helps to determine the ability of cells to incorporate the nanoparticles by endocytosis which may vary between different cell types. These positive control particles produced a bright fluorescent signal in HEK 293 cells (Figure 5C). Thus, the feasibility of the technology to record a specific fluorescent signal of an intracellular gene with a negligible background signal was confirmed. It must be mentioned that the difference between the background signal and the specific fluorescence decreases over time. The background increases due to probe degradation or incomplete quenching while the specific fluorescence fades gradually (Figure 5D). The same GAPDH-specific nanoparticles have been tested in primary fibroblast cultures of murine, porcine and ovine origin 17. These cells produce a much higher background signal than HEK 293 cells while the target-specific fluorescence is rather weak, possibly due to the relatively low proliferative capacity of these cultures.
These pilot experiments prompted us to use this technology for the detection of pluripotency gene expression in iPS derived from different species. For this purpose NANOG and GDF3 were analyzed, both of which are known to be expressed in pluripotent cells 18. At first iPS cells derived from tail-tip fibroblasts of an Nkx2.5 cardiac enhancer transgenic mouse line 19 were investigated. For both genes a strong fluorescent signal was obtained (Figure 6A) and a negligible Cy3-fluorescence of the scramble control (data not shown). Similar results were obtained on human and porcine iPS cells (Figure 6B and C). Importantly, the fluorescence signal was restricted to the iPS colonies and did not label the fibroblasts used as a feeder layer for mouse and porcine iPS (see arrows in Figure 6A and C). The analysis of NANOG gene expression also revealed that not every sequence predicted in silico to be &#8220;good&#8221; finally is functional. One of three designs of a NANOG-specific nanoparticles induced almost no fluorescent signal comparable to that of the scramble control despite a 100% sequence match in murine iPS cells (Figure 6D). A similar result was obtained on iPS cells of human and porcine origin with this probe (data not shown). Thus, nanoparticles can be used to detect pluripotency gene expression across species borders while the functionality of every single designed probe needs to be evaluated beforehand.
The promising results of the in situ labeling of live cells in cell culture dishes prompted us to analyze gene expression quantitatively by flow cytometry. To this end GAPDH-specific nanoparticles were added at graded concentrations to HEK 293 monolayers in order to compare the labeling efficiency within the target cell population. As assessed by fluorescent microscopy an enhanced Cy3-induced fluorescence was seen with the lowest concentration compared to cells which did not receive the nanoparticles. Increasing concentrations of the nanoparticles induced a clearly concentration dependent fluorescence of HEK 293 cells in situ (Figure 7A). Subjecting these cells to a flow cytometric analysis confirmed the concentration dependent labeling efficiency. The frequency of Cy3 positive cells increased significantly (more than sevenfold) when the highest concentration of nanoparticles was applied (Figure 7B). In further experiments ES cells from the Nkx2.5 cardiac enhancer transgenic mouse line 19 were used to analyze the expression of pluripotency genes by flow cytometry. Pilot experiments with 400 pM of the positive uptake control yielded clearly Cy3 positive live ES colonies under the microscope and flow cytometry detected almost 40% of Cy3 positive cells (Figure 7C). In contrast, comparable to untreated cells approximately 0.1% of cells treated with the scramble stained positive (data not shown). Similarly the addition of nanoparticles specific for Gapdh, Nanog and Gdf3 induced a distinct fluorescence signal in individual colonies in the cell culture dish. The frequency of Cy3 positive cells for Gapdh as determined by flow cytometry was comparable to that seen for both pluripotency genes (Figure 7C). This result is expectable as Nanog and Gdf3 are also thought to be expressed constitutively in pluripotent ES cells. Thus, these data clearly indicate that cells expressing a particular gene can be identified by flow cytometric analyses, qualitatively and by their relative amount.
<img alt="Figure 1" src="/files/ftp_upload/53268/53268fig1.jpg" /> 
Figure 1: Schematic Representation of the Structure of the Nanoparticles. (A) Structure of a gene-specific nanoparticle. (B) Scramble nanoparticle (negative control). (C) Uptake nanoparticle (positive control). Adapted from Lahm et al. 17, reprinted with permission from Wiley.
<img alt="Figure 2" src="/files/ftp_upload/53268/53268fig2.jpg" /> 
Figure 2: Application of Nanoparticles to Cell Cultures. A properly diluted solution of nanoparticles is pipetted simply into the culture medium. After O/N incubation gene-specific fluorescent cells are visible under a fluorescent microscope.
<img alt="Figure 3" src="/files/ftp_upload/53268/53268fig3.jpg" /> 
Figure 3: Active Uptake of Nanoparticles by Cells via Endocytosis. (A) Cells actively engulf the nanoparticles by endocytosis. (B) Target mRNA binds to the capture strand and displaces the fluorescing reporter.
<img alt="Figure 4" src="/files/ftp_upload/53268/53268fig4.jpg" /> 
Figure 4: Gating Strategy for Flow Cytometry. (A) Strategy for HEK 293 cells. (B) Strategy for murine ES cells. Data were acquired using device 1 for HEK 293 cells or device 2 for murine ES cells and were subsequently analyzed by a software tool (see Table of Materials).
<img alt="Figure 5" src="/files/ftp_upload/53268/53268fig5.jpg" /> 
Figure 5: Analysis of GAPDH-expression in HEK 293 Cells. A GAPDH-specific nanoparticle was added to the cells at 100 pM (final concentration) and fluorescence was recorded after O/N incubation. (A)GAPDH-specific nanoparticle. (B) Scramble (negative control). (C) Uptake (positive control). (D) Kinetics of scramble and uptake control. Fluorescence was determined at the indicated time-points after addition of GAPDH-specific nanoparticles. Scale bars represent 50 &#181;M.
<img alt="Figure 6" src="/files/ftp_upload/53268/53268fig6.jpg" /> 
Figure 6: Analysis of Pluripotency Gene Expression in iPS Cells of Different Species. Nanoparticles specific for NANOG or GDF3 were added to the cells at 400 pM (final concentration) and fluorescence was recorded after O/N incubation. (A) Murine iPS cells. (B) Human iPS cells. (C) Porcine iPS cells. Arrows in (A) and (C) designate unlabeled fibroblast feeder-layer cells. (D) Fluorescence in murine iPS cells after addition of the NANOG-design SF3 nanoparticle. Scale bars represent 50 &#181;M.
<img alt="Figure 7" src="/files/ftp_upload/53268/53268fig7.jpg" /> 
Figure 7: Nanoparticle Labeled Live Cells can be Identified by Flow Cytometry. (A) Microscopic view of Cy3 positive HEK 293 cells after addition of different concentrations of nanoparticles. (B) Frequency of Cy3 positive cells determined by flow cytometry. (C) Live staining of murine ES cell colonies and determination of the frequency of Cy3 positive cells. Nanoparticles were added at a final concentration of 400 pM. Scale bars represent 50 &#181;M.

Watch this Scientific Journal Video about Detection of Intracellular Gene Expression in Live Cells of Murine, Human and Porcine Origin Using Fluorescence-labeled Nanoparticles at JoVE.com

Detection of Intracellular Gene Expression in Live Cells of Murine, Human and Porcine Origin Using Fluorescence-labeled Nanoparticles

This manuscript describes a novel technique which allows the detection of intracellular gene expression after endocytosis of fluorescence-labeled nanoparticles directly in live cells. The method does not require manipulation of the cells and is not restricted with respect to the target gene or species.

The reprogramming of somatic cells to induced pluripotent stem cells (iPS) has successfully been performed in different mammalian species including mouse, ...

detection-intracellular-gene-expression-live-cells-murine-human

Research

JoVE Journal

Biology

The Preparation of Primary Hematopoietic Cell Cultures From Murine Bone Marrow for Electroporation

It is becoming increasingly apparent that electroporation is the most effective way to introduce plasmid DNA or siRNA into primary cells. The Gene Pulser MXcell  electroporation system and Gene Pulser  electroporation buffer were specifically developed to transfect nucleic acids into mammalian cells and difficult-to-transfect cells, such as primary and stem cells.This video demonstrates how to establish primary hematopoietic cell cultures from murine bone marrow, and then prepare them for electroporation in the MXcell system. We begin by isolating femur and tibia. Bone marrow from both femur and tibia are then harvested and cultures are established. Cultured bone marrow cells are then transfected and analyzed.

This procedure describes how to establish primary hematopoietic cell cultures from murine bone marrow and is followed by transfection using the Gene Pulser MXCell electroporation system.

It is becoming increasingly apparent that electroporation is the most effective way to introduce plasmid DNA or siRNA into primary cells. The Gene Pulser ...

Using the Gene Pulser MXcell Electroporation System to Transfect Primary Cells with High Efficiency

It is becoming increasingly apparent that electroporation is the most effective way to introduce plasmid DNA or siRNA into primary cells. The Gene Pulser MXcell electroporation system and Gene Pulser electroporation buffer (Bio-Rad) were specifically developed to easily transfect nucleic acids into mammalian cells and difficult-to-transfect cells, such as primary and stem cells. We will demonstrate how to perform a simple experiment to quickly identify the best electroporation conditions. We will demonstrate how to run several samples through a range of electroporation conditions so that an experiment can be conducted at the same time as optimization is performed. We will also show how optimal conditions identified using 96-well electroporation plates can be used with standard electroporation cuvettes, facilitating the switch from electroporation plates to electroporation cuvettes while maintaining the same electroporation efficiency. In the video, we will also discuss some of the key factors that can lead to the success or failure of electroporation experiments.

This procedure shows how to use the Gene Pulser MXcell electroporation system to rapidly and easily identify the best electroporation conditions for mouse embryonic fibroblasts (MEFs) or other primary cells. Considerations for troubleshooting are also discussed in the associated video.

Using an Automated Cell Counter to Simplify Gene Expression Studies: siRNA Knockdown of IL-4 Dependent Gene Expression in Namalwa Cells

The use of siRNA mediated gene knockdown is continuing to be an important tool in studies of gene expression.  siRNA studies are being conducted not only to study the effects of downregulating single genes, but also to interrogate signaling pathways and other complex interaction networks.  These pathway analyses require both the use of relevant cellular models and methods that cause less perturbation to the cellular physiology.  Electroporation is increasingly being used as an effective way to introduce siRNA and other nucleic acids into difficult to transfect cell lines and primary cells without altering the signaling pathway under investigation. There are multiple critical steps to a successful siRNA experiment, and there are ways to simplify the work while improving the data quality at several experimental stages.  To help you get started with your siRNA mediated gene knockdown project, we will demonstrate how to perform a pathway study complete from collecting and counting the cells prior to electroporation through post transfection real-time PCR gene expression analysis.  The following study investigates the role of the transcriptional activator STAT6 in IL-4 dependent gene expression of CCL17 in a Burkitt lymphoma cell line (Namalwa).  The techniques demonstrated are useful for a wide range of siRNA-based experiments on both adherent and suspension cells.  We will also show how to streamline cell counting with the TC10 automated cell counter, how to electroporate multiple samples simultaneously using the MXcell electroporation system, and how to simultaneously assess RNA quality and quantity with the Experion automated electrophoresis system.

This procedure describes a quick and easy workflow to introduce siRNA into difficult to transfect cell lines and follow gene expression by real-time PCR. Use of an automated cell counter, multi-well electroporation plate, and automated electrophoresis station provide quick and reliable results without the need for expensive robotic handling.

The use of siRNA mediated gene knockdown is continuing to be an important tool in studies of gene expression.  siRNA studies are being conducted not only ...

Chromatin Immunoprecipitation (ChIP) to Assay Dynamic Histone Modification in Activated Gene Expression in Human Cells

In response to a variety of extracellular ligands, the STAT (signal transducer and activator of transcription) transcription factors are rapidly recruited from their latent state in the cytoplasm to cell surface receptors where they are activated by phosphorylation at a single tyrosine residue1. They then dimerize and translocate to the nucleus to drive the transcription of target genes, affecting growth, differentiation, homeostasis and the immune response. Not surprisingly, given their widespread involvement in normal cell processes, dysregulation of STAT function contributes to human disease, particularly to cancers2 and autoimmune diseases3. It is well established that transcription is regulated by alterations to the chromatin template4,5. These alterations include the activities of ATP-dependent complexes, as well as covalent histone modifications and DNA methylation6. Because STAT activation of gene expression is both rapid and transient, it requires specific mechanisms for modulating the chromatin template at STAT-dependent gene loci. To define these mechanisms, we characterize the histone modifications and the enzymatic activities that generate them at gene loci that respond to STAT signaling. This protocol describes chromatin immunoprecipitation, a method that is valuable for the study of STAT signaling to chromatin in activated gene expression.

Chromatin Immunoprecipitation ChIP to Assay Dynamic Histone Modification in Activated Gene Expression in Human Cells

This protocol describes how chromatin immunoprecipitation (ChIP) is used to study the dynamic alterations to the chromatin template that regulate transcription induced by a signal transduction pathway.

In response to a variety of extracellular ligands, the STAT (signal transducer and activator of transcription) transcription factors are rapidly recruited ...

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

The number of significant genetic associations with common complex traits is constantly increasing. However, most of these associations have not been understood at molecular level. One of the mechanisms mediating the effect of DNA variants on phenotypes is gene expression, which has been shown to be particularly relevant for complex traits1.
This method tests in a cellular context the effect of specific DNA sequences on gene expression. The principle is to measure the relative abundance of transcripts arising from the two alleles of a gene, analysing cells which carry one copy of the DNA sequences associated with disease (the risk variants)2,3. Therefore, the cells used for this method should meet two fundamental genotypic requirements: they have to be heterozygous both for DNA risk variants and for DNA markers, typically coding polymorphisms, which can distinguish transcripts based on their chromosomal origin (Figure 1). DNA risk variants and DNA markers do not need to have the same allele frequency but the phase (haplotypic) relationship of the genetic markers needs to be understood. It is also important to choose cell types which express the gene of interest. This protocol refers specifically to the procedure adopted to extract nucleic acids from fibroblasts but the method is equally applicable to other cells types including primary cells.
DNA and RNA are extracted from the selected cell lines and cDNA is generated. DNA and cDNA are analysed with a primer extension assay, designed to target the coding DNA markers4. The primer extension assay is carried out using the MassARRAY (Sequenom)5 platform according to the manufacturer's specifications. Primer extension products are then analysed by matrix-assisted laser desorption/ionization time of-flight mass spectrometry (MALDI-TOF/MS). Because the selected markers are heterozygous they will generate two peaks on the MS profiles. The area of each peak is proportional to the transcript abundance and can be measured with a function of the MassARRAY Typer software to generate an allelic ratio (allele 1: allele 2) calculation. The allelic ratio obtained for cDNA is normalized using that measured from genomic DNA, where the allelic ratio is expected to be 1:1 to correct for technical artifacts. Markers with a normalised allelic ratio significantly different to 1 indicate that the amount of transcript generated from the two chromosomes in the same cell is different, suggesting that the DNA variants associated with the phenotype have an effect on gene expression. Experimental controls should be used to confirm the results.

Genetic associations often remain unexplained at a functional level. This method aims to assess the effect of phenotype-associated genetic markers on gene expression by analyzing cells heterozygous for transcribed SNPs. The technology allows accurate measurement by MALDI-TOF mass spectrometry to quantify allele-specific primer extension products.

The number of significant genetic associations with common complex traits is constantly increasing. However, most of these associations have not been ...

Paraffin-Embedded and Frozen Sections of Drosophila Adult Muscles

The molecular characterization of muscular dystrophies and myopathies in humans has revealed the complexity of muscle disease and genetic analysis of muscle specification, formation and function in model systems has provided valuable insight into muscle physiology. Therefore, identifying and characterizing molecular mechanisms that underlie muscle damage is critical. The structure of adult Drosophila multi-fiber muscles resemble vertebrate striated muscles 1 and the genetic tractability of Drosophila has made it a great system to analyze dystrophic muscle morphology and characterize the processes affecting muscular function in ageing adult flies 2. Here we present the histological technique for preparing paraffin-embedded and frozen sections of Drosophila thoracic muscles. These preparations allow for the tissue to be stained with classical histological stains and labeled with protein detecting dyes, and specifically cryosections are ideal for immunohistochemical detection of proteins in intact muscles. This allows for analysis of muscle tissue structure, identification of morphological defects, and detection of the expression pattern for muscle/neuron-specific proteins in Drosophila adult muscles. These techniques can also be slightly modified for sectioning of other body parts.

Paraffin-Embedded and Frozen Sections of Drosophila Adult Muscles

Identification of mechanisms underlying muscle damage is crucial. Here we present the histological technique for preparing paraffin-embedded and frozen sections of Drosophila thoracic muscles. This allows analysis of muscle morphology and localization of protein and other muscle cell components.

The molecular characterization of muscular dystrophies and myopathies in humans has revealed the complexity of muscle disease and genetic analysis of ...

In vitro Reconstitution of the Active T. castaneum Telomerase

Efforts to isolate the catalytic subunit of telomerase, TERT, in sufficient quantities for structural studies, have been met with limited success for more than a decade. Here, we present methods for the isolation of the recombinant Tribolium castaneum TERT (TcTERT) and the reconstitution of the active T. castaneum telomerase ribonucleoprotein (RNP) complex in vitro.
Telomerase is a specialized reverse transcriptase1 that adds short DNA repeats, called telomeres, to the 3' end of linear chromosomes2 that serve to protect them from end-to-end fusion and degradation. Following DNA replication, a short segment is lost at the end of the chromosome3 and without telomerase, cells continue dividing until eventually reaching their Hayflick Limit4. Additionally, telomerase is dormant in most somatic cells5 in adults, but is active in cancer cells6 where it promotes cell immortality7.
The minimal telomerase enzyme consists of two core components: the protein subunit (TERT), which comprises the catalytic subunit of the enzyme and an integral RNA component (TER), which contains the template TERT uses to synthesize telomeres8,9. Prior to 2008, only structures for individual telomerase domains had been solved10,11. A major breakthrough in this field came from the determination of the crystal structure of the active12, catalytic subunit of T. castaneum telomerase, TcTERT1.
Here, we present methods for producing large quantities of the active, soluble TcTERT for structural and biochemical studies, and the reconstitution of the telomerase RNP complex in vitro for telomerase activity assays. An overview of the experimental methods used is shown in Figure 1.

In vitro Reconstitution of the Active T. castaneum Telomerase

Efforts to isolate the catalytic subunit of telomerase, TERT, in sufficient quantities for structural studies, have been met with limited success for more than a decade. Here, we present methods for the isolation of the recombinant Tribolium castaneum TERT (TcTERT) and the reconstitution of the active T. castaneum telomerase ribonucleoprotein (RNP) complex in vitro.

Efforts to isolate the catalytic subunit of telomerase, TERT, in sufficient quantities for structural studies, have been met with limited success for more ...

Analysis of Global RNA Synthesis at the Single Cell Level following Hypoxia

Hypoxia or lowering of the oxygen availability is involved in many physiological and pathological processes. At the molecular level, cells initiate a particular transcriptional program in order to mount an appropriate and coordinated cellular response. The cell possesses several oxygen sensor enzymes that require molecular oxygen as cofactor for their activity. These range from prolyl-hydroxylases to histone demethylases. The majority of studies analyzing cellular responses to hypoxia are based on cellular populations and average studies, and as such single cell analysis of hypoxic cells are seldom performed. Here we describe a method of analysis of global RNA synthesis at the single cell level in hypoxia by using Click-iT RNA imaging kits in an oxygen controlled workstation, followed by microscopy analysis and quantification.&nbsp; Using cancer cells exposed to hypoxia for different lengths of time, RNA is labeled and measured in each cell. This analysis allows the visualization of temporal and cell-to-cell changes in global RNA synthesis following hypoxic stress.

We describe a technique for analysis of global RNA synthesis in hypoxia using imaging. Click-chemistry labeling of RNA has not previously been performed under hypoxia and allows visualization of global RNA changes at the single cell level. This approach complements the existing averaged RNA techniques, allowing direct visualization of cell-to-cell changes in global RNA synthesis.

Hypoxia or lowering of the oxygen availability is involved in many physiological and pathological processes. At the molecular level, cells initiate a ...

siRNA Screening to Identify Ubiquitin and Ubiquitin-like System Regulators of Biological Pathways in Cultured Mammalian Cells

Post-translational modification of proteins with ubiquitin and ubiquitin-like molecules (UBLs) is emerging as a dynamic cellular signaling network that regulates diverse biological pathways including the hypoxia response, proteostasis, the DNA damage response and transcription.&#160; To better understand how UBLs regulate pathways relevant to human disease, we have compiled a human siRNA &#8220;ubiquitome&#8221; library consisting of 1,186 siRNA duplex pools targeting all known and predicted components of UBL system pathways. This library can be screened against a range of cell lines expressing reporters of diverse biological pathways to determine which UBL components act as positive or negative regulators of the pathway in question.&#160; Here, we describe a protocol utilizing this library to identify ubiquitome-regulators of the HIF1A-mediated cellular response to hypoxia using a transcription-based luciferase reporter.&#160; An initial assay development stage is performed to establish suitable screening parameters of the cell line before performing the screen in three stages: primary, secondary and tertiary/deconvolution screening. &#160;The use of targeted over whole genome siRNA libraries is becoming increasingly popular as it offers the advantage of reporting only on members of the pathway with which the investigators are most interested.&#160; Despite inherent limitations of siRNA screening, in particular false-positives caused by siRNA off-target effects, the identification of genuine novel regulators of the pathways in question outweigh these shortcomings, which can be overcome by performing a series of carefully undertaken control experiments.

Here, we describe a methodology to perform a targeted siRNA &#8220;ubiquitome&#8221; screen to identify novel ubiquitin and ubiquitin-like regulators of the HIF1A-mediated cellular response to hypoxia.&#160; This can be adapted to any biological pathway where a robust read out of reporter activity is available.

Post-translational modification of proteins with ubiquitin and ubiquitin-like molecules (UBLs) is emerging as a dynamic cellular signaling network that ...

Measurement of Metabolic Rate in Drosophila using Respirometry

Metabolic disorders are a frequent problem affecting human health. Therefore, understanding the mechanisms that regulate metabolism is a crucial scientific task. Many disease causing genes in humans have a fly homologue, making Drosophila a good model to study signaling pathways involved in the development of different disorders. Additionally, the tractability of Drosophila simplifies genetic screens to aid in identifying novel therapeutic targets that may regulate metabolism. In order to perform such a screen a simple and fast method to identify changes in the metabolic state of flies is necessary. In general, carbon dioxide production is a good indicator of substrate oxidation and energy expenditure providing information about metabolic state. In this protocol we introduce a simple method to measure CO2 output from flies. This technique can potentially aid in the identification of genetic perturbations affecting metabolic rate.

Measurement of Metabolic Rate in Drosophila using Respirometry

Metabolic disorders are among one of the most common diseases in humans. The genetically tractable model organism D. melanogaster can be used to identify novel genes that regulate metabolism. This paper describes a relatively simple method which allows studying the metabolic rate in flies by measuring their CO2 production.