Whole-cell Patch-clamp Recordings of Isolated Primary Epithelial Cells from the Epididymis

摘要

We present a protocol that combines cell isolation and whole-cell patch-clamp recording to measure the electrical properties of the primary dissociated epithelial cells from the rat cauda epididymides. This protocol allows for investigation of the functional properties of primary epididymal epithelial cells to further elucidate the physiological role of the epididymis.

摘要

The epididymis is an essential organ for sperm maturation and reproductive health. The epididymal epithelium consists of intricately connected cell types that are distinct not only in molecular and morphological features but also in physiological properties. These differences reflect their diverse functions, which together establish the necessary microenvironment for the post-testicular sperm development in the epididymal lumen. The understanding of the biophysical properties of the epididymal epithelial cells is critical for revealing their functions in sperm and reproductive health, under both physiological and pathophysiological conditions. While their functional properties have yet to be fully elucidated, the epididymal epithelial cells can be studied using the patch-clamp technique, a tool for measuring the cellular events and the membrane properties of single cells. Here, we describe the methods of cell isolation and whole-cell patch-clamp recording to measure the electrical properties of primary dissociated epithelial cells from the rat cauda epididymides.

引言

The epididymis in the male reproductive tract is an organ lined with a layer of mosaic epithelial cells. As in other epithelial tissues, the various cell types of the epididymal epithelium, including principal cells, clear cells, basal cells and cells from the immunological and lymphatic systems, work in a concerted manner to function as the barrier at the tubule frontline and as the supporting cells for sperm maturation and physiology^1,2,3. Thus, these epithelial cells play an essential role in reproductive health.

Epithelial cells are generally regarded as non-excitable cells that are unable to generate all-or-none action potentials in response to depolarizing stimuli, due to a lack of voltage-gated Na⁺ or Ca²⁺ channels^4,5. However, epithelial cells express unique sets of ion channels and transporters that regulate their specialized physiological roles, such as secretion and nutrient transportation⁶. Different epithelial cells therefore possess characteristic electrical properties. For example, the principal cells express the CFTR for fluid and chloride transportation and express the TRPV6 for calcium reabsorption, whereas the clear cells express the proton pump V-ATPase for luminal acidification^1,7,8,9. Some transporters and ion channels that regulate the physiological features of the epididymal epithelial cells have been reported, but the functional properties of epididymal epithelial cells are largely not yet understood^10,11,12,13.

Whole-cell patch-clamp recording is a well-established technique for examining the intrinsic properties of both excitable and non-excitable cells, and is particularly helpful for studying the functions of primarily dissociated cells in heterogeneous cell samples; the voltage-clamp is used for measuring the passive membrane properties and the ionic currents of single cells^14,15. The passive membrane properties include input resistance and capacitance. The former parameter indicates the intrinsic membrane conductance, while the latter implies the surface area of the cell membrane (a phospholipid bilayer, where ion channels and transporters are located, that serves as a thin insulator separating extracellular and intracellular media). The membrane capacitance is directly proportional to the cell membrane's surface area. Together with the membrane resistance that is reflected by the input resistance, the membrane time constant, which indicates how fast the cell membrane potential responds to the flow of ion channel currents, can be determined. In this regard, by combining the current response characteristics from a series of voltage steps applied to the cells, the biophysical kinetics and properties of the cells are determined^15,16,17,18.

In the present paper, we describe the procedures for isolating epithelial cells from the rat cauda epididymis and the steps for measuring the membrane properties of different cell types in the dissociated cell mixture using the whole-cell patch-clamp. We show that the epididymal principal cells exhibit distinct membrane electrophysiological properties and that the conductances can be readily identified from other cell types.

方案

All animal experiments are carried out in accordance with the guidelines of the ShanghaiTech University Institutional Animal Care and Use Committee, which fulfill the local and international requirements.

1. Experimental Animals

1. Use adult male Sprague-Dawley rats (~300-450 g) between 8-12 weeks old. At this age in the rats, the sperm have arrived in the cauda epididymides.

2. Isolation of Epithelial Cells from Rat Cauda Epididymides

NOTE: The following steps are performed under non-aseptic conditions unless otherwise stated.

1. Preparation of dissection instruments and reagents
   1. Disinfect the dissection tools by immersion in 70% ethanol and let them air dry.
   2. Turn on the warming bath (32 °C); Prepare and pre-warm 500 mL of 1x Roswell Park Memorial Institute 1640 Medium (RPMI) supplemented with 1% (v/v) antibiotics (100 U/mL penicillin and 100 µg/mL streptomycin final), and labeled as "RPMI (+P/S 1:100)". Perform this step in a clean air-flow controlled working station.
   3. Prepare and pre-warm 1x 500 mL Iscove's Modified Dulbecco's Medium (IMDM) containing non-essential amino acids (0.1 mM) and sodium pyruvate (1 mM), and supplemented with 5-α-dihydrotestosterone (1 nM), 10% fetal bovine serum, 1% (v/v) antibiotics (100 U/mL penicillin and 100 µg/mL streptomycin final), and labeled as "Full-IMDM". Create 50 mL aliquots and seal with parafilm; store at 4 °C. Use aseptic conditions.
   4. Prepare a collagenase enzyme digestion solution by dissolving collagenase Type I and collagenase Type II in RPMI (+P/S 1:100) resulting in 1 mg/mL of each collagenase in the solution. Filter through a 0.22-µm membrane and mark as "Collagenase Solution". Keep at room temperature (RT) until use. Adjust the volume of the enzyme solution based on the weight of the enzyme; the minimal volume required for both cauda epididymides from a single rat is 2 mL.
   5. Fill a 35 mm dish with RPMI (+P/S 1:100).
2. Dissection of rat cauda epididymides
   1. Sacrifice the animal by either using sodium pentobarbital 85 mg/kg i.p. or using an isoflurane chamber until the animal does not respond to tail-pinching stimulation; follow by cervical dislocation.
   2. Disinfect the lower abdomen by wiping with 70% ethanol, gently push the two testes down to the lower abdomen, and then open the lower abdomen near the scrotum.
   3. Pick up the epididymal fat, dissect out the whole reproductive organs (testes, epididymides, and vas deferens) and immerse in the dish with RPMI (+P/S 1:100).
   4. Transfer the reproductive organs in the dish with RPMI (+P/S 1:100) to an aseptic working station.
   5. Dissect out the cauda epididymides from the connective and fatty tissues and the epididymal capsule. Place one epididymis with ~0.2 mL of Collagenase Solution in a 1.5 mL tube.Perform this step in a clean air-flow controlled working station.
3. Dissociation of single cells from rat cauda epididymides
   1. Cut the epididymides in the Collagenase Solution using fine scissors until the tissue becomes a paste-like fluid. Rinse the scissors gently with the rest of (~0.8 mL) enzyme solution in the 1.5 mL tube.
   2. Place the tube on a metal thermomixer for 30 min at 37 °C with a shaking speed of 1,000 rpm.
   3. Centrifuge the enzyme-tissue mixture at 30 x g at RT for 3 min and decant the sticky supernatant that contains mostly the sperm.
   4. Resuspend the pellet in 1 mL Full-IMDM to quench all the enzymatic activity. Transfer the cell suspension to a 50 mL tube containing 49 mL RPMI (+P/S 1:100).
      NOTE: Optionally, filter the cell suspension through a 100 µm mesh membrane with constant trituration to avoid large, cell aggregates. However, do not use a mesh filter if cell suspension is needed for growing cell monolayers.
   5. Centrifuge the cellular mixture at 30 x g at RT for 10 min; decant the supernatant.
   6. Resuspend the pellet in 1 mL Full-IMDM with gentle trituration for at least 5 min to dissociate single cells from the enzymatic treated epididymal tissue mixtures.
4. Separation of epithelial cells from other cells under aseptic conditions
   1. Culture the cell suspension on a 10 cm Petri dish containing Full-IMDM for at least 8 h or overnight, in an incubator at 32 °C in 5% CO₂.
   2. Prepare sterile coverslips in advance by immersion in 100% alcohol. Air dry and dip in a small volume of the culture medium. Place the coverslips in 6 cm culture dishes or in single wells of a 24-well plate.
   3. Next morning, harvest the dissociated epithelial cells by gently collecting the cell suspension from the Petri dish, which consists mostly of epithelial cells. Centrifuge the cell suspension at 30 x g at RT for 5 min, and then decant the supernatant.
   4. Resuspend the cell pellet in ~2 mL Full-IMDM.
   5. Seed 0.2 mL of the harvested cell suspension onto the center of each sterile coverslip.
   6. Let the cell suspension settle in the liquid droplet for at least 10 min to allow cells to loosely adhere to the glass coverslips. Carefully add 1 mL Full-IMDM at the edge of 10 cm dish, or 0.3 mL Full-IMDM to each well of a 24-well plate; do not disturb cells.
   7. Keep the isolated single cells on coverslips in the incubator at 32 °C in 5% CO₂ until the patch-clamp experiments.

3. Recording Solutions and Micropipettes

NOTE: For the patch-clamp experiments, use the best quality chemicals and solutions.

1. Preparation of stock solutions
   1. Autoclave all the bottles for stock storage and filter all the stock solutions (except the corrosive solutions) and filter through 0.22-µm membranes before use.
   2. Prepare all stock solutions in advance at RT, and store at 4 ^oC: 5 M NaCl; 1 M KCl; 100 mM MgCl₂; 100 mM CaCl₂; 200 mM NaH₂PO₄; 100 mM EGTA (pH 7.0 with KOH). Handle 5 M NaOH, 1 M HCl and 1 M KOH stocks as corrosive solutions.
2. Preparation of standard external recording physiological salt solution (PSS)
   1. Warm the stock solutions to RT on the morning of the patch-clamp recording.
   2. Pipette the ingredients from each stock according to the desired final volume, except CaCl₂, e.g. for preparing 500 mL of PSS: 140 mM NaCl = 14 mL of 5M; 5 mM KCl = 2.5 mL of 1M; 1.2 mM MgCl₂ = 6 mL of 100 mM; 1.2 mM NaH₂PO₄ = 3 mL of 200 mM.
   3. Add double-distilled water (ddH₂O) to the final volume of 400 mL and equilibrate.
   4. Weigh 0.9 g glucose and 1.19 g HEPES and dissolve completely in the solution mixture.
   5. Add the CaCl₂ stock (2.5 mM = 12.5 mL of 100 mM) with stirring.
   6. Add up to 99% of final volume.
   7. Adjust the pH to 7.4 using NaOH or HCl.
   8. Check the osmolarity and adjust using 5 M NaCl or glucose, if necessary.
   9. Add ddH₂O to the final volume of 500 mL in a cylinder.
3. Preparation of micropipette internal solutions (low EGTA K⁺ -based solutions)
   1. Weigh or pipette the correct volume of the reagents from each stock according to the desired final volume and concentration, e.g. for preparing 50 mL low EGTA K⁺-based intracellular solution to a volume of ~ 30 mL ddH₂O: 100 mM K-gluconate = 1.17 g; 35 mM KCl = 1.75 mL of 1 M; 2 mM MgCl₂ = 1 mL of 100 mM; 0.1 mM EGTA = 0.05 mL of 100 mM; 10 mM HEPES = 0.072 g.
   2. Add enough water for ~ 95% of final volume and allow the solution to equilibrate at RT. Make sure that the solution is clear.
   3. While constantly stirring the solution, adjust the pH to 7.2 using KOH.
   4. Weigh and add 0.078 g Mg-ATP to the solution until it is dissolved completely.
   5. Place the solution on ice and use a small aliquot for the measurement of osmolarity; typically, the solutions measures ~290 mOsmol and does not need adjustment. If the osmolarity differs significantly from 280-295 mOsmol, prepare a new solution.
   6. Add ddH₂O to final volume.
   7. Divide the solution into 500 µL aliquots, filter with a 0.2 µm syringe filter, tightly seal and immediately store at ≤ -20 °C.
   8. On the date of the patch-clamp experiment, thaw one aliquot of intracellular solution on ice and keep chilled during the patch-clamp experiment to prevent degradation.
4. Pull the patch pipettes from glass capillaries (following pipette puller user's manual) to obtain micropipette sizes with resistance of 5-10 M when filled with intracellular solution.

4. Setting up the Patch-Clamp Experiment and Establishing Whole-Cell Configuration with Cells

1. Setting up the patch-clamp experiment
   1. Turn on the patch-clamp set up (computer, computer-controlled amplifier, digitizer, etc.)
   2. Open the patch-clamp software (e.g. AXON pCLAMP10 or HEKA PatchMaster) and set up the protocols for electrophysiological recordings. Set the filter for the signal to low pass at 1-3 kHz and the digitizer at 10-20 kHz.
   3. Turn on the camera, micromanipulator and light source.
   4. When the computer-controlled amplifier is on, ground the body of experimenter by touching with hands the patch-clamp rig that has been grounded, before touching the headstage, in order to protect it from electrical shocks.
   5. Transfer the culturing epithelial cells on the glass coverslip to the recording chamber filled with ~1 mL of standard PSS at RT. Carefully change the bathing PSS at least two times using a pipette before any patch-clamp experiments.
      NOTE: Optionally, fill the perfusion system with standard PSS or another external solution according to the planned experiment. Perfuse the microscope-mounted recording chamber (RC-26G or RC-26GLP) with PSS a few times at a speed of ~2 mL/min before the start off the patch-clamp experiments. Make sure that there are no air bubbles trapped along the perfusion system.
   6. View and select the cells under an inverted microscope using 10X and 40X objectives equipped with a differential interference contrast optical system. Look for large single isolated cells for recording. Identify the isolated epididymal epithelial cells by their spherical shape with rough microvilli on one end of the membranes and polarized distribution of intracellular contents (Figure 1).
   7. Using a 1 mL syringe (a home-made nonmetallic microsyringe needle), fill a micropipette with the internal solution (low EGTA K⁺-based solution, see step 3.3). Make sure that there are no air bubbles in the micropipette, which can increase the resistance of the micropipette. Use enough solution so that the internal solution submerges the chloride-coated silver wire electrode within the micropipette holder.
   8. Mount the micropipette in the electrode holder, and apply a low positive pressure (~0.2 mL syringe volume). Keep the low positive pressure continuous until touching the cell membrane in the later steps.
2. Establishing whole-cell configuration with cells for recordings
   1. Immerse the pipette into the bath solution at the highest speed of the micromanipulator. Find the pipette tip in the screen connected to the digital camera; slow down the micromanipulator speed to the medium-high mode.
   2. Quickly check the micropipette resistance (5-10 MΩ) using the data acquisition interface command (e.g. "Membrane Test" in the AXON system) by applying a voltage step (e.g. 5 mV for 100 ms) generated from the computer-controlled amplifier. Change to a new micropipette if the resistance is significantly out of this range.
   3. Start to move down the objective mounted on the microscope; gradually guide the micropipette toward the selected cell. Always lower the objective first, and then lower the micropipette to the plane of focus, untilthe micropipette is above the center surface of the selected cell.
   4. Cancel the liquid junction potential between the pipette and bath solutions to zero using the "pipette offset" command in the commander interface of software.
   5. Set the computer-controlled amplifier commander to the voltage-clamp and the membrane test to the "Bath" mode.
   6. Fine focus for a clearer view of the cell, then gradually lower the micropipette using the micromanipulator at the low-medium speed.
   7. When the micropipette is close to the cell (demonstrated by a decreased current when triggered by the membrane test command), remove the low positive pressure immediately and apply a weak negative pressure (0.1 mL syringe volume) to form the gigaseal (>1 GΩ).
   8. Monitor the resistance with the membrane test. If the resistance is >500 MΩ but <1 GΩ, apply a negative potential (usually as the holding potential which is set to -60 mV), which can help form the gigaseal. Compensate the transient capacitive current of the micropipette.
   9. If the seal is >1 GΩ and stable (as shown in the software interface), apply a brief and strong suction in order to break the cell membrane. Do not apply compensation for the series resistance and the cell capacitance.
   10. Immediately after achieving a successful whole-cell configuration, apply a 10 mV hyperpolarizing step (5-traces with minimal time intervals, 20 ms duration, signal sample at 20 kHz) from a holding potential of -60 mV.
   11. Switch the voltage-mode to the zero-current mode and mark down the readings from the software interface or perform a gap-free recording (10-60 s) for the membrane potential readings of the cell.
   12. Quickly switch back to and remain in the voltage-mode and apply the voltage protocols according to the planned experiments and measure the current responses. Subtraction is not applied to the intrinsic leak current during the recordings.
   13. Monitor the stability of the responses during the recordings, or the different parameters of the cell. For example, use the "Membrane Test" command interface to check the input resistance (R_i), the series resistance (R_s) and the cell membrane capacitance (C_m) in the membrane test at the "Cell" mode during the switch of protocols.
       NOTE: Sudden drops in input resistance is usually indicative of a loose patch, and a dramatic increase in the series resistance may be indicative of micropipette tip clogging by the intracellular organelles or membrane fragments. During recording, regularly monitor the micropipette location to check if drift occurs, which may lead to the loss of the patch. If drift is a problem, carefully lift together the micropipette and the patching cell away from the bottom of recording chamber. This step may sometimes lead to the loss of the patch, in which case, it is necessary to repeat the whole-cell patch-clamp procedure.

5. Analysis of Passive Electrophysiological Properties of Cells

1. After obtaining the data from the patch-clamp experiments, open the gap-free data in the Clampfit software and measure the mean value for the resting membrane potential for each cell. Alternatively, use the value as marked down from the zero-current voltage at the current mode. Correct the values with the liquid junction potential (12.4 mV in this study).
2. Open the data from the 10-mV hyperpolarizing step (ΔV) obtained from a cell, measure the current difference before and during the step (ΔI_step), and calculate the input resistance (R_i) using the equation as:
   
3. Calculate the cell capacitance (C_m, in unit of pF) (use the same current data from the 10-mV hyperpolarizing step by integrating the total area under the membrane capacitor current during the initial transient decay current raised upon the voltage step trigger), to obtain the value of the total accumulated charge (Q, in unit of pA•ms) of the cell. Use the following equation:
   
4. Calculate the value of the series resistance (R_s) for each cell by fitting the initial transient current from the 10-mV negative step with a standard exponential algorithm to obtain the time constant decay current (T, in unit of ms) and use the following equation:
   

结果

The described enzymatic digestion procedure for the isolation of epithelial cells from the rat cauda epididymides is a modified protocol from our previous studies^9,12. This method produces a mixture of single cells with over 90% viability and without surface blisters or swollen cell volume. The heterogeneous cell mixture consists mainly of principal cells, clear cells and basal cells, as we have described previously

讨论

In this protocol, the enzymatic dispersion of the rat cauda epididymides consistently yielded healthy epithelial cells. The quality of the epididymal epithelial cells for the patch-clamp experiments is dependent on a few critical steps in the protocol. For instance, the centrifugation of the cell mixture at a low centrifugal force (30 x g) is important for removing the spermatozoa and the epididymal luminal content; the epididymal epithelial cells become unhealthy in the presence of the spermatozoa in the cell culture. I...

材料

本文使用的材料清单

姓名	公司	目录编号	评论
<强>AXON 系统仪器
计算机控制放大器	分子器件 - Axon	Multiclamp 700B 膜片钳放大器
数字采集系统	分子器件 - Axon	Digidata 1550 转换器
显微镜	奥林巴斯	BX-61WI
显微作器	萨特仪器	MPC-325
记录室和在线加热器	华纳仪器	TC-324C
HEKA 系统仪器
膜片钳放大器	哈佛生物科学 - HEKA	EPC-10 USB 双
显微镜	奥林巴斯	IX73
显微作器	Sutter Instruments	MPC-325
记录室和在线加热器	Warner Instruments	TC-324C
其他仪器
微量移液器拉拔器	Sutter 仪器	P-1000
记录室	华纳仪器	RC-26G 或自制室
硼硅酸盐毛细管玻璃带细丝	萨特仪器 / 哈佛仪器	BF150-86-10
隔振台	TMC	63544
Digital Camare	HAMAMASTU	ORCA-Flash4.0 V2 C11440-22CU
试剂
RPMI 1640 培养基	Gibco	22400089
青霉素/链霉素	Gibca	15140112
	;	2005 年 30 月
IMDM	Gibco	C12440500BT
胶原酶 I	Sigma	C0130
胶原酶 II	Sigma	C6885
5-&α;-二氢睾酮	Medchemexpress	HY-A0120
胎牛血清	摩羯座	FBS-12A
<强>微量移液器内部溶液（基于 K+ 的溶液）（pH 7.2,280-295 mOsm）
KCl，35 mM	Sigma/各种	V900068
MgCl2 · 6H2O，2 mM	Sigma/各种	M2393
EGTA，0.1 mM	Sigma/各种	E4378
HEPES，10 mM	Sigma/各种	V900477
葡萄糖酸钾盐，100 mM	Sigma/各种	P-1847
Mg-ATP，3 mM	Sigma/各种	A9187
标准外部记录生理盐溶液 （PSS）（pH 7.4,300-310 mOsm）
NaCl，140 mM	Sigma/各种	V900058
KCl，4.7 mM	Sigma/各种	V900068
CaCl2，2.5 mM	Sigma/各种	V900266
MgCl2 · 6H2O，1.2 mM	Sigma/各种	M2393
NaH2PO4,1.2 mM	Sigma/各种	V900060
HEPES，10 mM	Sigma/各种	V900477
葡萄糖、10mM	Sigma/各种	V900392
<强>用于 pH 调节
NaOH	Sigma/各种	V900797	纯度 >=97%
KOH	Sigma/各种	60371	纯度 >=99.99%