This study was supported by grants from the National Natural Science Foundation of China (82204951) and Sichuan Science and Technology Program (2020JDRC0102).

Adult C57BL/6 mice (6 weeks of age, 25-30 g) were used in this study. All procedures were performed in compliance with local regulations of animal welfare and experimental ethics. The study was approved by the West China Hospital of Sichuan University Biomedical Research Ethics Committee.
1. Glomeruli labeling and tissue preparation
<ol>
	<li>Glomeruli labeling
	<ol>
		<li>Dissolve FITC-dextran (10 mg) in 1x phosphate-buffered saline (PBS) at a ratio of 1:1 (1 mg: 1 mL) to p...

Fluorescent Labeling of Glomeruli in Cleared Mouse Kidneys for Microscopy

<ol>
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F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glomerular+number+and+size+in+relation+to+age,+kidney+weight,+and+body+surface+in+normal+man.">Glomerular number and size in relation to age, kidney weight, and body surface in normal man.</a> The Anatomical Record. 232 (2), 194-201 (1992).</li><li>Rasch, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Prevention+of+diabetic+glomerulopathy+in+streptozotocin+diabetic+rats+by+insulin+treatment.+Kidney+size+and+glomerular+volume.">Prevention of diabetic glomerulopathy in streptozotocin diabetic rats by insulin treatment. Kidney size and glomerular volume.</a> Diabetologia. 16 (2), 125-128 (1979).</li><li>Puelles, V. G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glomerular+number+and+size+variability+and+risk+for+kidney+disease.">Glomerular number and size variability and risk for kidney disease.</a> Current Opinion in Nephrology and Hypertension. 20 (1), 7-15 (2011).</li><li>Bertram, J. F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Why+and+how+we+determine+nephron+number.">Why and how we determine nephron number.</a> Pediatric Nephrology. 29, 575-580 (2014).</li><li>Bertram, J. F., Soosaipillai, M. C., Ricardo, S. D., Ryan, G. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Total+numbers+of+glomeruli+and+individual+glomerular+cell+types+in+the+normal+rat+kidney.">Total numbers of glomeruli and individual glomerular cell types in the normal rat kidney.</a> Cell and Tissue Research. 270 (1), 37-45 (1992).</li><li>Nyengaard, J. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Stereologic+methods+and+their+application+in+kidney+research.">Stereologic methods and their application in kidney research.</a> Journal of the American Society of Nephrology. 10 (5), 1100-1123 (1999).</li><li>Bertram, J. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Analyzing+renal+glomeruli+with+the+new+stereology.">Analyzing renal glomeruli with the new stereology.</a> International Review of Cytology. 161, 111-172 (1995).</li><li>L&#248;drup, A. B., Karstoft, K., Dissing, T. H., Pedersen, M., Nyengaard, J. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Kidney+biopsies+can+be+used+for+estimations+of+glomerular+number+and+volume:+a+pig+study.">Kidney biopsies can be used for estimations of glomerular number and volume: a pig study.</a> Virchows Archiv. 452 (4), 393-403 (2008).</li><li>Lane, P. H., Steffes, M. W., Mauer, S. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Estimation+of+glomerular+volume:+a+comparison+of+four+methods.">Estimation of glomerular volume: a comparison of four methods.</a> Kidney International. 41 (4), 1085-1089 (1992).</li><li>Baldelomar, E. J., Charlton, J. R., deRonde, K. A., Bennett, K. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+vivo+measurements+of+kidney+glomerular+number+and+size+in+healthy+and+Os(/+)+mice+using+MRI.">In vivo measurements of kidney glomerular number and size in healthy and Os(/+) mice using MRI.</a> American Journal of Physiology-Renal Physiology. 317 (4), F865-F873 (2019).</li><li>Huang, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+cationic+near+infrared+fluorescent+agent+and+ethyl-cinnamate+tissue+clearing+protocol+for+vascular+staining+and+imaging.">A cationic near infrared fluorescent agent and ethyl-cinnamate tissue clearing protocol for vascular staining and imaging.</a> Scientific Reports. 9 (1), 521 (2019).</li><li>Beeman, S. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Measuring+glomerular+number+and+size+in+perfused+kidneys+using+MRI.">Measuring glomerular number and size in perfused kidneys using MRI.</a> American Journal of Physiology-Renal Physiology. 300 (6), F1454-F1457 (2011).</li><li>Basgen, J. M., Steffes, M. W., Stillman, A. E., Mauer, S. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Estimating+glomerular+number+in+situ+using+magnetic+resonance+imaging+and+biopsy.">Estimating glomerular number in situ using magnetic resonance imaging and biopsy.</a> Kidney International. 45 (6), 1668-1672 (1994).</li><li>Prentice, B. M., Caprioli, R. M., Vuiblet, V. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Label-free+molecular+imaging+of+the+kidney.">Label-free molecular imaging of the kidney.</a> Kidney International. 92 (3), 580-598 (2017).</li><li>Sanden, S. K., Wiggins, J. E., Goyal, M., Riggs, L. K., Wiggins, R. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Evaluation+of+a+thick+and+thin+section+method+for+estimation+of+podocyte+number,+glomerular+volume,+and+glomerular+volume+per+podocyte+in+rat+kidney+with+Wilms'+tumor-1+protein+used+as+a+podocyte+nuclear+marker.">Evaluation of a thick and thin section method for estimation of podocyte number, glomerular volume, and glomerular volume per podocyte in rat kidney with Wilms' tumor-1 protein used as a podocyte nuclear marker.</a> Journal of the American Society of Nephrology. 14 (10), 2484-2493 (2003).</li><li>Hama, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Scale:+a+chemical+approach+for+fluorescence+imaging+and+reconstruction+of+transparent+mouse+brain.">Scale: a chemical approach for fluorescence imaging and reconstruction of transparent mouse brain.</a> Nature Neuroscience. 14 (11), 1481-1488 (2011).</li><li>Susaki, E. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Whole-brain+imaging+with+single-cell+resolution+using+chemical+cocktails+and+computational+analysis.">Whole-brain imaging with single-cell resolution using chemical cocktails and computational analysis.</a> Cell. 157 (3), 726-739 (2014).</li><li>Lloyd-Lewis, B., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Imaging+the+mammary+gland+and+mammary+tumours+in+3D:+optical+tissue+clearing+and+immunofluorescence+methods.">Imaging the mammary gland and mammary tumours in 3D: optical tissue clearing and immunofluorescence methods.</a> Breast Cancer Research. 18 (1), 127 (2016).</li><li>Ren, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CUBIC-plus:+An+optimized+method+for+rapid+tissue+clearing+and+decolorization.">CUBIC-plus: An optimized method for rapid tissue clearing and decolorization.</a> Biochemical and Biophysical Research Communications. 568, 116-123 (2021).</li><li>Azaripour, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+survey+of+clearing+techniques+for+3D+imaging+of+tissues+with+special+reference+to+connective+tissue.">A survey of clearing techniques for 3D imaging of tissues with special reference to connective tissue.</a> Progress in Histochemistry and Cytochemistry. 51 (2), 9-23 (2016).</li><li>Matsumoto, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Advanced+CUBIC+tissue+clearing+for+whole-organ+cell+profiling.">Advanced CUBIC tissue clearing for whole-organ cell profiling.</a> Nature Protocols. 14 (12), 3506-3537 (2019).</li><li>Puelles, V. G., Moeller, M. J., Bertram, J. 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S., Lichtman, J. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Clarifying+tissue+clearing.">Clarifying tissue clearing.</a> Cell. 162 (2), 246-257 (2015).</li><li>Kolesov&#225;, H., Olejn&#237;&#269;kov&#225;, V., Kvasilov&#225;, A., Gregorovi&#269;ov&#225;, M., Sedmera, D. J. I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tissue+clearing+and+imaging+methods+for+cardiovascular+development.">Tissue clearing and imaging methods for cardiovascular development.</a> Iscience. 238 (2), 489-507 (2021).</li><li>Tian, T., Yang, Z., Li, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tissue+clearing+technique:+Recent+progress+and+biomedical+applications.">Tissue clearing technique: Recent progress and biomedical applications.</a> Journal of Anatomy. 238 (2), 489-507 (2021).</li><li>Du, H., Hou, P., Zhang, W., Li, Q. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Advances+in+CLARITY-based+tissue+clearing+and+imaging.">Advances in CLARITY-based tissue clearing and imaging.</a> Experimental and Therapeutic. 16 (3), 1567-1576 (2018).</li><li>Ert&#252;rk, A., Lafkas, D., Chalouni, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Imaging+cleared+intact+biological+systems+at+a+cellular+level+by+3DISCO.">Imaging cleared intact biological systems at a cellular level by 3DISCO.</a> Journal of Visualized Experiments: JoVE. 89, e51382 (2014).</li></ol>

Tissue-clearing technologies can be classified into 3 or 4 groups29,30,31. Organic solvent-based tissue clearing (e.g., DISCO and PEGASOS), aqueous-based tissue clearing (e.g., CUBIC), and hydrogel embedding tissue clearing (e.g., CLARITY) have all been applied in kidney clearing 25,26,28,32. CUBIC, as...

The number and volume of glomeruli are very important for the diagnosis and treatment of various kidney diseases1,2,3,4,5. The golden standard of glomeruli number estimation is the physical dissector/fractionator combination. However, this method requires special reagents and equipment, making it slow and expensive6,7,8,9. Biopsy provides a wealth of information, but obviously, this method is only suitable for rough estimations10,11. Medical imaging technologies, including magnetic resonance imaging (MRI), computed tomography (CT), and X-ray, are also widely used in glomerular detection12,13,14,15, but such technologies require bulky instruments. New methods, such as matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometer16 or the thick and thin section method17, have also been used in glomerular detection, though they remain tedious and laborious.
With the help of transparency technologies, it is possible to observe deeper depths and obtain richer and more complete information from thick tissues or even whole organs18,19,20,21,22,23. Therefore, transparency technologies have been widely used in kidney research24. The observation and detection of glomeruli in the cleared kidneys are also involved. However, these published articles either only briefly referred to glomerular detection25 or used difficult-to-achieve labeling methods such as transgenic animals26, self-produced dyes13, or high-concentration antibody incubation27 to label the glomeruli. In addition, although studies had analyzed glomeruli in cleared kidneys, the analyses were always limited13 or relied on analysis algorithms established by the authors themselves26.
We have previously demonstrated a more convenient way to label the glomeruli in mice kidneys28. By using Imaris, we found that glomeruli count, frequency, and volume could be quickly obtained. Thus, here we present a more accessible, comprehensive, and simplified set of methods to label and analyze the glomeruli of mice kidneys.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>4% PFA</td>
			<td>Biosharp</td>
			<td>7007171800</td>
			<td>Fixation reaagen</td>
		</tr>
		<tr>
			<td>502 Glue&#160;</td>
			<td>Deli</td>
			<td>7146</td>
			<td>For fixing the kidney to the sample fixing adapter&#160;</td>
		</tr>
		<tr>
			<td>Antipyrine</td>
			<td>Aladdin</td>
			<td>A110660</td>
			<td>Clearing reagent</td>
		</tr>
		<tr>
			<td>Brain Matrix</td>
			<td>RWD Life Science</td>
			<td>1mm 40-75</td>
			<td>Tissue slicing</td>
		</tr>
		<tr>
			<td>Confocal microscopy</td>
			<td>Nikon</td>
			<td>A1plus</td>
			<td>Image acquisition</td>
		</tr>
		<tr>
			<td>FITC-Dextran</td>
			<td>Sigma-Aldrich</td>
			<td>FD150S</td>
			<td>Labeling reagent</td>
		</tr>
		<tr>
			<td>Light sheet fluorescence microscopy&#160;</td>
			<td>Zeiss</td>
			<td>Light sheet 7&#160;</td>
			<td>Image acquisition</td>
		</tr>
		<tr>
			<td>Mice</td>
			<td>Ensiweier</td>
			<td></td>
			<td>Adult C57BL/6 mice (6 weeks of age, 25&#8211;30 g)&#160;</td>
		</tr>
		<tr>
			<td>N-Butyldiethanolamine</td>
			<td>Aladdin</td>
			<td>B299095</td>
			<td>Clearing reagent</td>
		</tr>
		<tr>
			<td>Nicotinamide</td>
			<td>Aladdin</td>
			<td>N105042</td>
			<td>Clearing reagent</td>
		</tr>
		<tr>
			<td>Pentobarbital Natriumsalz</td>
			<td>Sigma-Aldrich</td>
			<td>P3761</td>
			<td></td>
		</tr>
		<tr>
			<td>Tail vein fixator</td>
			<td>JINUOTAI</td>
			<td>JNT-FS35</td>
			<td>Fix the mouse for vail injection</td>
		</tr>
		<tr>
			<td>Triton X-100</td>
			<td>Sigma-Aldrich</td>
			<td>T8787</td>
			<td>Clearing reagent</td>
		</tr>
	</tbody>
</table>

an efficient and fast method for labeling and analyzing mouse glomeruli

The glomeruli are fundamental units in the kidney; hence, studying the glomeruli is pivotal for understanding renal function and pathology. Biological imaging provides intuitive information; thus, it is of great significance to label and observe the glomeruli. However, the glomeruli observation methods currently in use require complicated operations, and the results may lose label details or three-dimensional (3D) information. The clear, unobstructed brain imaging cocktails and computational analysis (CUBIC) tissue clearing technology has been widely used in renal research, allowing for more accurate detection and deeper detection depth. We found that mouse glomeruli can be rapidly and effectively labeled by tail vein injection of medium molecular weight FITC-Dextran followed by the CUBIC clearing method. The cleared mouse kidney could be scanned by a light-sheet microscope (or a confocal microscope when sliced) to obtain three-dimensional image stacks of all the glomeruli in the entire kidney. Processed with appropriate software, the glomeruli signals could be easily digitized and further analyzed to measure the number, volume, and frequency of the glomeruli.

Author Spotlight: Aiding Research in Kidney Biology by Labeling Glomeruli in Cleared Tissues 

An Efficient and Fast Method for Labeling and Analyzing Mouse Glomeruli

Labeling and counting glomeruli using conventional methods can be complicated, tedious, time consuming, and bulky instrument are required. Our method offers an instant and intuitively accurate labeling method for analysis of the glomeruli within the entire kidney. Our technique is a quick, easy, accurate, and cheap method to analyze glomeruli in the entire kidney.It does not require any special equipment, so it can be carried out in any laboratory. This is a groundbreaking, rapid, and simple method to label glomeruli, allowing for an intuitive observation of all the glomeruli within the entire kidney. It holds great potential to assist researchers to make significant breakthroughs in the study of the kidney by providing information such as glomeruli quantity, volume, distribution, and more.On one hand, we're exploring the application of this glomeruli labeling method in clinical kidney disease research. On the other hand, we'll keep working on enhancing methods to label biotargets like blood vessels or specific proteins in transparent tissues, adjusting them to meet our research needs.

This study provides a simple and efficient method for labeling and analyzing the glomeruli in mice kidneys.
Glomeruli (blood vessels) can be well labeled by intravascularly injected FITC-Dextran. After the clearing process, the kidney became transparent (Figure 1A), and the glomeruli could be clearly observed by using light-sheet microscopy (Figure 1B) or confocal microscopy (Figure 1C). Confocal microsco...

Watch this Scientific Journal Video about Aiding Research in Kidney Biology by Labeling Glomeruli in Cleared Tissues at JoVE.com

This study presents an easy-to-use, complete, and simple set of methods to label and analyze glomeruli from CUBIC-cleared mouse kidneys. Data such as glomerulus number and volume can be obtained easily and reliably using fluorescein isothiocyanate (FITC)-Dextran, light sheet fluorescence microscopy (LSFM), or common confocal microscopy and software such as Imaris.

The glomeruli are fundamental units in the kidney; hence, studying the glomeruli is pivotal for understanding renal function and pathology. Biological ...

an-efficient-fast-method-for-labeling-analyzing-mouse

Research

JoVE Journal

Biology

669 ビュー.  Sichuan University. 従来の方法を使用した糸球体のラベリングとカウントは、複雑で退屈で時間がかかり、かさばる機器が必要になる場合があります。私たちの方法は、腎臓全体の糸球体を分析するための即時かつ直感的に正確な標識法を提供します。私たちの技術は、腎臓全体の糸球体を分析するための迅速、簡単、正確、そして安価な方法です。特別な機器を必要としないため、?...

ビデオ: 著者スポットライト:クリアされた組織に糸球体を標識することにより、腎臓生物学の研究を支援する 

This study presents an easy-to-use, complete, and simple set of methods to label and analyze glomeruli from CUBIC-cleared mouse kidneys. Data such as glomerulus number and volume can be obtained easily and reliably using fluorescein isothiocyanate (FITC)-Dextran, light sheet fluorescence microscopy (LSFM), or common confocal microscopy and software such as...

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glomeruli isolation: a technique to obtain intact glomeruli from murine kidney

This video describes the method to isolate intact glomeruli from mouse kidneys. The encapsulated and decapsulated glomeruli thus obtained can further be used for culturing parietal epithelial cell outgrowths from the murine...

Glomeruli Isolation: A Technique to Obtain Intact Glomeruli from Murine Kidney

isolation of glomeruli and in vivo labeling of glomerular cell surface proteins

Isolation of Glomeruli and In Vivo Labeling of Glomerular Cell Surface Proteins

Here we present a protocol for murine in vivo labeling of glomerular cell surface proteins with biotin. This protocol contains information on how to perfuse mouse kidneys, isolate glomeruli, and perform endogenous immunoprecipitation of the protein of...

Isolation of Glomeruli and In Vivo Labeling of Glomerular Cell Surface Proteins

Next, transfer the kidneys to a 100-millimeter Petri dish and use two scalpels to mince them into small pieces that are approximately 1 to 2 millimeters. Keep the minced kidney pieces wet with...

an efficient sieving method to isolate intact glomeruli from adult rat kidney

An Efficient Sieving Method to Isolate Intact Glomeruli from Adult Rat Kidney

The main focus of this protocol is to efficiently isolate viable primary glomeruli cultures with minimal contaminants for use in a variety of downstream applications. The isolated glomeruli retain structural relationships between component cell types and can be cultured ex vivo for a short...

microrna in situ hybridization for formalin fixed kidney tissues

MicroRNA In situ Hybridization for Formalin Fixed Kidney Tissues

This article describes an in situ hybridization protocol optimized for colormetric detection of microRNA expression in formalin fixed kidney...

MicroRNA In situ Hybridization for Formalin Fixed Kidney Tissues

kidney regeneration in adult zebrafish by gentamicin induced injury

Kidney Regeneration in Adult Zebrafish by Gentamicin Induced Injury

Here we present a reliable method to study adult kidney regeneration by inducing acute kidney injury by gentamicin injection. We show that injury is dependent on gentamicin dosage and environmental temperature using in situ hybridization to label lhx1a+ developing new nephrons.

enhanced 3d confocal imaging of solvent-cleared human heart tissues

Enhanced 3D Confocal Imaging of Solvent-Cleared Human Heart Tissues

bilateral renal ischemia-reperfusion model for acute kidney injury in mice

Author Spotlight: Bilateral Renal Ischemia-Reperfusion Model for Acute Kidney Injury in Mice

The ischemia-reperfusion injury (IRI) model can be used at different stages of acute kidney injury (AKI) development, especially during AKI to chronic kidney disease (CKD) progression. Here, we describe the procedure for IRI model development in mice via a trans-abdominal approach, clamping renal pedicles via a vascular clip to induce ischemic...

Developing Murine Acute Kidney Injury Model Using Bilateral Ischemia-Reperfusion

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single-channel analysis and calcium imaging in the podocytes of the freshly isolated glomeruli

Single-channel Analysis and Calcium Imaging in the Podocytes of the Freshly Isolated Glomeruli

Changes in the intracellular calcium levels in the podocytes are one of the most important means to control the filtration function of glomeruli. Here we explain a high-throughput approach that allows detection of real-time calcium handling and single ion channels activity in the podocytes of the freshly isolated glomeruli.

acute kidney injury model induced by cisplatin in adult zebrafish

Acute Kidney Injury Model Induced by Cisplatin in Adult Zebrafish

This protocol describes the procedures to induce Acute Kidney Injury (AKI) in adult zebrafish using cisplatin as a nephrotoxic agent. We detailed the steps to evaluate the reproducibility of the technique and two techniques to analyze inflammation and cell death in the renal tissue, flow cytometry and TUNEL,...

pipeline for multi-scale three-dimensional anatomic study of the human heart

Author Spotlight: Advancing Human Cardiac Anatomy Through Multi-Scale Analysis of Hearts

This protocol presents a comprehensive pipeline to analyze samples obtained from human hearts that span the microscopic and macroscopic...

Comprehensive 3D Analysis of Human Hearts from Micro to Macro Scales

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assessment of kidney function in mouse models of glomerular disease

Assessment of Kidney Function in Mouse Models of Glomerular Disease

This protocol describes a full kidney work-up that should be carried out in mouse models of glomerular disease. The methods allow for detailed functional, structural, and mechanistic analysis of glomerular function, which can be applied to all mouse models of glomerular...

formation of human thymus organoids in three-dimensional fibrin hydrogels

Author Spotlight: Advancing Thymic Epithelial Cells and T-Cell Research with Human Thymic Organoids

Here, we describe a protocol for the formation of human iPSC-derived thymus organoids grown in 3D fibrin hydrogels aiming to support thymic epithelial cell (TEC) maturation and prolonged maintenance, as well as thymopoiesis in...

Recreating the Thymic Microenvironment with iPSC-Derived Organoids

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orienteering as a tool for cognitive research: an implementation guide

Author Spotlight: Utilizing Orienteering in Research to Improve Brain Health and Spatial Memory

The sport of orienteering is emerging as an effective way to train both the body and brain as it combines physical activity with spatial navigation. The current manuscript offers a guide on how to implement the sport of orienteering in...

Implementing Orienteering for Body and Brain Training 

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ex vivo placental explant flow culture - mimicking the dynamic conditions in utero

Author Spotlight: Advancing Research Through Single Cell Sequencing and Spatial Histology in Placental Tissues 

Here is a protocol for culturing placental explants under constant flow conditions. This approach enhances traditional static villous culture systems by enabling the replication of dynamic physiological...

Improving Ex Vivo Placental Explant Culture Using a Flow-Based Approach

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systems biology of metabolic regulation by estrogen receptor signaling in breast cancer

Systems Biology of Metabolic Regulation by Estrogen Receptor Signaling in Breast Cancer

Integration of data from genome-wide sequencing experiments and metabolomics experiments is a challenge.  In this paper we report, for the first time, generation, analysis and integration of transcriptome, cistrome and metabolome data from breast cancer cells treated with estradiol.

estimation of nephron number in whole kidney using the acid maceration method

Estimation of Nephron Number in Whole Kidney using the Acid Maceration Method

Estimates of whole kidney nephron number are important clinically and experimentally, as there is an inverse association between nephron number and an enhanced risk of renal and cardiovascular disease.Herein, the use of the acid maceration method, which provides fast and reliable estimates of whole kidney nephron number, is...