Assay to Measure Nucleocytoplasmic Transport in Real Time within Motor Neuron-like NSC-34 Cells

Summary

This protocol describes a method to sensitively measure the nucleocytoplasmic transport rate within motor neuron-like NSC-34 cells by quantifying the real-time change in the nuclear import of a NLS-NES-GFP protein.

Abstract

Nucleocytoplasmic transport refers to the import and export of large molecules from the cell nucleus. Recently, a number of studies have shown a connection between amyotrophic lateral sclerosis (ALS) and impairments in the nucleocytoplasmic pathway. ALS is a neurodegenerative disease affecting the motor neurons and resulting in paralysis and ultimately in death, within 2-5 years on average. Most cases of ALS are sporadic, lacking any apparent genetic linkage, but 10% are inherited in a dominant manner. Recently, hexanucleotide repeat expansions (HREs) in the chromosome 9 open reading frame 72 (C9orf72) gene were identified as a genetic cause of ALS and frontotemporal dementia (FTD). Importantly, different groups have recently proposed that these mutants affect nucleocytoplasmic transport. These studies have mostly shown the final outcome and manifestations caused by HREs on nucleocytoplasmic transport, but they do not demonstrate nuclear transport dysfunction in real time. As a result, only severe nucleocytoplasmic transport deficiency can be determined, mostly due to high overexpression or exogenous protein insertion.

This protocol describes a new and very sensitive assay to evaluate and quantify nucleocytoplasmic transport dysfunction in real time. The rate of import of a NLS-NES-GFP protein (shuttle-GFP) can be quantified in real time using fluorescent microscopy. This is performed by using an exportin inhibitor, thus allowing the shuttle GFP only to enter the nucleus. To validate the assay, the C9orf72 HRE translated dipeptide repeats, poly(GR) and poly(PR), which have been previously shown to disrupt nucleocytoplasmic transport, were used. Using the described assay, a 50% decrease in the nuclear import rate was observed compared to the control. Using this system, minute changes in nucleocytoplasmic transport can be examined and the ability of different factors to rescue (even partially) a nucleocytoplasmic transport defect can be determined.

Introduction

The nuclear pore complex (NPC) controls the import and export of large molecules into and out of the cell nucleus. In contrast to small molecules, which can enter the nucleus without regulation¹, the transport of larger molecules is strongly controlled by the NPC. These large molecules, such as proteins and RNA, associate with transport factors, including importins and exportins, to be imported and exported from the nucleus². In order to be imported, proteins must contain a small peptide motif, generally called a nuclear localization signal (NLS), which is bound by importins². These sequences of amino acids act as a tag and are diverse in composition^3,4. Proteins can be exported from the nucleus to the cytoplasm due to their association with exportins, which bind a signal sequence, generally called a nuclear export signal (NES)². Both importins and exportins are able to transport their cargo due to the regulation of the small Ras related nuclear protein GTPase (Ran)². Ran has been shown to exist in different conformational states depending on whether it is bound to GTP or GDP. When bound to GTP, Ran can bind to importins or exportins. Upon binding to RanGTP, importins release their cargo, while exportins must bind RanGTP to form a complex with their export cargo. The dominant nucleotide binding state of Ran depends on its location in the nucleus (RanGTP) or the cytoplasm (RanGDP).

Recently, a number of studies have shown a connection between impairments in the nucleocytoplasmic pathway and both amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD)^{5,6,7,8,9,10,11,12}. ALS is a progressive and fatal neurodegenerative disease affecting both upper and lower motor neurons (MNs)¹³ and resulting in paralysis and ultimately in death, within 2-5 years on average. Most cases of ALS are classified as sporadic (SALS), lacking any apparent genetic linkage, but 10% are inherited in a dominant manner (familial ALS; FALS). Recently, hexanucleotide repeat expansions (HREs) in the chromosome 9 open reading frame 72 (C9orf72) gene were identified^14,15 as a genetic cause of ALS and FTD. These mutants account for 30-40% of FALS cases¹⁶, and different studies have contended that they cause toxicity by affecting nucleocytoplasmic transport^{5,6,7,8,9,10,11,12}.

These studies have mostly shown the final outcomes and manifestations of HREs on nucleocytoplasmic transport, but they do not demonstrate nucleocytoplasmic disruption in real time. As a result, only severe nucleocytoplasmic transport deficiency has been evaluated^11,17,18.

This protocol describes a new and very sensitive assay to evaluate and quantify nucleocytoplasmic transport dysfunction in real time. The rate of import of a NLS-NES-GFP protein (shuttle-GFP) can be quantified in real time using fluorescent microscopy. This is done using an exportin inhibitor, as described previously¹⁸, thus allowing the shuttle-GFP only to enter the nucleus. Using florescent microscopy and a software capable of quantifying fluorescent changes in real time, it is possible to quantify gradual changes in the fluorescence intensity of the shuttle-GFP, located in the nucleus. As a result, a Michaelis-Menten-like saturation curve of the fluorescence-to-time axis, representing the amount of nuclear shuttle-GFP at any given time, can be made. By using the initial linear rate of the curves, it is possible to generate a slope, which represents the rate of entry into the nucleus before fluorescence saturation.

To validate the assay, the translated C9orf72 dipeptide repeats, poly(GR) and poly(PR), which have been previously reported to disrupt nucleocytoplasmic transport, were used^5,7,8,10,12. Using this assay, a 50% decrease in the nuclear import rate was observed compared to the control. Using this system, minute changes in nucleocytoplasmic transport can be examined. Moreover, the ability of different factors to rescue a nucleocytoplasmic transport defect can be determined.

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Protocol

1. Cell Line Preparation

1. Thaw approximately 1,000,000 mouse neuroblastoma spinal cord cells (NSC-34 cells) that were stored in a liquid nitrogen container. Use a 37 °C water incubator until the cells are fully thawed.
2. Add fresh, warm medium (DMEM medium containing 10% fetal bovine serum (FBS), 1% L-glutamine, and 1% pen-strep antibiotics).
3. Centrifuge thawed cells (SL16R) at 500 x g for 5 min, forming a cell pellet. Discard the medium and add 1 mL of new medium for the cell resuspension.
4. Place the resuspended cells in a 15 mL flask and add an extra 5 mL of medium. Incubate the cells overnight in a sterile incubator with 5% CO₂ at 37 °C.
5. In parallel, place 8 uncoated coverslips (cover glass: 12 mm, 0.13-0.17 mm thick) in a 60-mm culture dish and sterilize using 70% ethanol and exposure to 30 min of UV light until it is dry. Add medium to each dish and dispose to wash off the residual ethanol.
6. Add trypsin buffer (2.5 g of trypsin and 0.2 g of EDTA in 1 L of Hanks' Balanced Salt Solution) to the cells after they reach approximately 90% confluence (roughly 6 million cells per flask) to allow adherent cells to dissociate.
   NOTE: NSC-34 cells are sensitive and only require 15 s of trypsin buffer incubation and 1 additional min of incubation free of trypsin before dissociation using the medium.
7. Plate the cells onto the 60 mm culture dishes already containing the coverslips with 3 mL of medium, approximately 350,000 per dish. Leave them in the incubator for 24 h to allow cell attachment onto the coverslips.

2. Cell Transfection

NOTE: After approximately 24 h, the NSC-34 cells will reach 40% confluence (approximately 800,000 cells) and will be ready for transfection.

1. Prepare pure DMEM medium (300 µL of DMEM medium for each 60 mm culture dish) in sterile microcentrifuge tubes.
2. Add 2 µg of each plasmid required for transfection to each DMEM-containing microcentrifuge tube.
   NOTE: The shuttle-GFP plasmid is mandatory in all cell transfections.
3. Add transfection reagent to all the microcentrifuge tubes that contain their required plasmids. Here, add 4 µL of the commercial transfection reagent for each 2 µg of DNA.
4. Vortex the microcentrifuge tubes containing DMEM, plasmids, and the transfection reagent and incubate them at room temperature for 25 min.
5. Add each microcentrifuge tube to a culture dish and stir the dish gently to form a homogenous solution. Place the dish back in the incubator for 48 h.
   NOTE: Since shuttle-GFP should be expressed in all cells, the shuttle-GFP transfection efficiency can be partially examined and pre-tested using fluorescent microscopy after overnight transfection. A full examination of non-fluorescent expressed proteins can be conducted using an immunoblot analysis.

3. Microscopy

1. Attach the coverslips containing transfected NSC-34 cells to a coverslip holder and wash gently with phosphate-buffered saline (PBS) to remove the detached dead cells.
2. Identify a suitable cell patch using a green fluorescent filter with an inverted microscope.
   NOTE: A suitable cell patch is defined as a microscope field of view showing a large number of cells (20-30 cells in a field) and in which the nuclei are clearly defined in the cells. Cell nuclei within the cell patch are first identified by eye and are manually marked by the imaging software.
3. Add 200 µL of an exportin-1 inhibitor Leptomycin B (LMB) buffer containing 10 ng/mL LMB in PBS to the coverslips by dripping the buffer on the coverslips under the microscope.
   NOTE: This point in time is set as interval zero.
4. Quantify the fluorescent intensity of the marked nuclei in 3 s intervals for around 400-500 s.
5. Test between 3 and 5 cover slips for each transfection group in each individual experiment.

4. Analysis

NOTE: Since different cells express different levels of florescent shuttle-GFP, it is important to normalize the nuclear fluorescent intensity of each cell to its own initial fluorescent intensity.

1. Normalize the fluorescent intensity of the marked nuclei by dividing 3-s fluorescent interval of each nucleus with the average of the initial six intervals of that nucleus.
2. After the normalization of each nucleus, produce a fluorescent intensity curve representing the change in nuclei fluorescence as a function of time for each cell patch. To do this, calculate the average of all the cells in each cell-patch (consisting of approximately 20-30 cells in each patch).
   NOTE: The nuclei fluorescent intensity curve resembles a Michaelis-Menten saturation curve, which is better observed within increased time periods. This is due to a decrease in the cytosolic amounts of shuttle-GFP with time due to nuclear transport. This decrease statistically lowers the probability of a shuttle-GFP to transport into the nucleus, thus reaching saturation in nuclear fluorescence. The slope derived from the linear initial rate of the curve yields the V_max entry rate into the nucleus.
3. Analyze the V_max slopes of each cell patch, derived from three to five independent experiments, using the graphing software to produce one slope representing each experimental group. Perform quantification using one-way ANOVA statistical analysis.

5. Protein Expression Validation

1. Place 60 mm culture dishes containing the residual cells (not used in the above experiment) from each experimental group on ice.
2. Dispose the medium and wash the cells twice with PBS to dilute and wash the remaining medium.
3. Treat the cells with 200-400 µL of lysis buffer containing PBS, 0.5% Triton, and protease inhibitor cocktail tablet (PI). Scrape using a cell scraper.
4. Collect the cells in lysis buffer in a microcentrifuge tube and homogenize with a homogenizer at 4,000 rpm for 1 min under ice.
5. Centrifuge the homogenized cells at 2,500 x g for 10 min. Collect the supernatant, quantify the protein concentration using a Bradford assay, and store until use at -20 °C.
6. Collect between 30 and 70 µg of total protein (depending on the protein) and load it into a SDS-PAGE gel to test for protein expression using an immunoblot assay.

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Results

Using the procedure presented here, motor neuron-like NSC-34 cells were transfected with a NLS-NES-GFP (shuttle-GFP) protein. This protein, which has NLS and NES signal sequences (Figure 1), can shuttle between the nucleus and the cytoplasm. Generic GFP can enter or exit the nucleus in the absence of any localization signal tag only by diffusion and is therefore distributed evenly between the nucleus and the cytoplasm (Figure 2A). In contrast, the shuttle...

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Discussion

This protocol demonstrates a highly sensitive and quantitative new assay to evaluate minute changes in nucleocytoplasmic transport. Using this system, it is possible to observe and measure nucleocytoplasmic transport and its dysfunction in real time, not only large defects that result in dramatic changes in protein distribution. This assay not only has a sensitivity advantage, but it also requires little preparation, is inexpensive, and is a very easy and low-engagement assay.

To test the effi...

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Materials

Name	Company	Catalog Number	Comments
Mouse Motor Neuron-Like hybrid Cell Line (NSC-34)	tebu-bio	CLU140-A
DMEM 4.5 g/L L-glucose	Biological Industries	01-055-1A
FBS European Grade	Biological Industries	04-007-1A
SL 16R Centrifuge	Thermo Scientific	75004030
Thermo Forma Series ii Water Jacketed CO2 Incubator	Thermo Scientific	3111
Cover glass 12 mm dia., 0.13-0.17 mm thick	Bar Naor LTD
TurboFect Transfection Reagent	Thermo Scientific	R0531
Axiovert 100 inverted microscope	Zeiss
Imaging Workbench 2	Axon Instruments
Leptomycin B	Sigma	L2913
PBS	Biological Industries	02-023-1A
Homogenizer motor/control/chuck/90 degree clamp	Glas-Col	099C K5424CE
MicroCL 17R Centrifuge, Refrigerated	Thermo Scientific	75002455