Single-cell Microinjection for Cell Communication Analysis

Summary

We describe here how to perform a single-cell microinjection of Lucifer Yellow to visualize cellular communication via gap-junctions in living cells, and provide some useful tips. We expect that this paper will help everyone to evaluate the degree of cellular coupling due to functional gap junctions. Everything described here could be, in principle, adapted to other fluorescent dyes with molecular weight below 1,000 Daltons.

Abstract

Gap junctions are intercellular channels that allow the communication of neighboring cells. This communication depends on the contribution of a hemichannel by each neighboring cell to form the gap junction. In mammalian cells, the hemichannel is formed by six connexins, monomers with four transmembrane domains and a C and N terminal within the cytoplasm. Gap junctions permit the exchange of ions, second messengers, and small metabolites. In addition, they have important roles in many forms of cellular communication within physiological processes such as synaptic transmission, heart contraction, cell growth and differentiation. We detail how to perform a single-cell microinjection of Lucifer Yellow to visualize cellular communication via gap-junctions in living cells. It is expected that in functional gap junctions, the dye will diffuse from the loaded cell to the connected cells. It is a very useful technique to study gap junctions since you can evaluate the diffusion of the fluorescence in real time. We discuss how to prepare the cells and the micropipette, how to use a micromanipulator and inject a low molecular weight fluorescent dye in an epithelial cell line.

Introduction

Gap junctions are intercellular channels that allow the intercommunication among neighboring cells¹. This communication connects two or more neighboring cells, where each one contributes with a connexon or hemichannel to form the intercellular channel. In mammalian cells, the connexon is formed by six connexins, monomers with four transmembrane domains and a C and N terminal within the cytoplasm². Gap junctions not only permit the flow of ions, second messengers and small metabolites, but also contribute to many forms of cellular communication in many physiological processes, such as synaptic transmission, heart contraction, cell growth and differentiation^3,4,5,6,7,8. In addition gap junctions have been associated with many diseases including cancer^9,10, muscular atrophy¹¹, some genetic diseases and demyelinating diseases¹².

This type of intercellular crosstalk can be evaluated by several methods^13,14,15,16. In this paper, we show how to perform a single-cell microinjection of Lucifer Yellow to visualize cellular communication via gap-junctions in living cells. We discuss how to prepare the cells and the micropipette, the usage of the micromanipulator and the injection of Lucifer Yellow dye in a thymic epithelial cell line. Usually, this experimental procedure could be analyzed by the average of connected cells to the cell loaded with dye. In addition, this method could be used with other fluorescent dyes with molecular weight below the gap junctions cut-off which is approximately 1,000 daltons.

Protocol

1. Preparation of Cells

1. Maintain a culture of a thymic epithelial cell line (IT76M1) or cell to be tested in an incubator (37°C/5% CO₂).
2. Wash the cells with PBS 1x (repeat this item 3x).
3. Add Trypsin to the cells for 5 min.
4. Add medium (twice of the volume of trypsin added in item 1.3) with 10% FBS (fetal bovine serum) to the cells with trypsin and centrifuge (800 x g for 5 min).
5. Count the cells in a hemocytometer.
6. Adjust the density of cells according to the cell type as the cells have to be in close contact with each other to allow coupling. Note: In our case, we used 3 x 10⁵ cells per 35 mm Petri dish.

2. Micropipette Preparation

1. Pull the micropipette as specified from a glass capillary micropipette (1.5 mm diameter) to a final 0.2 µm of diameter so as to attain a final resistance of approximately 30 MΩ^17,18.
   NOTE: Alternatively, injection pipettes can be purchased. The resistance depends on the cell size, for instance a higher resistance microelectrode would be necessary for pancreatic acinar cells, for example (100-150 MΩ)¹⁹. A common problem that could occur is the precipitation of Lucifer Yellow solution which can then obstruct the micropipette and may require prior filtration or centrifugation. Before injection, the micropipette should be analyzed under the microscope to detect if there is an obstruction or any type of disruption¹³. The micropipette can be tested by injecting LY with the micropipette tip inside a saline solution.

3. Testing the Micropipette

1. Prepare the Lucifer Yellow solution (5%) in 150 mmol/L LiCI and load the micropipette using a syringe or by backfilling (put into it LY Solution).
2. Place the micropipette over the 35 mm Petri dish with the IT76M1 cells on the microinjection workstation and submerge the tip of the glass micropipette into the cell medium. Focus on the micropipette and perform a dye flowing test by applying a pulse.

4. Single-cell Lucifer Yellow Microinjection

1. Focus the microscope right above the cell layer using a high magnification (40X), then slowly lower the pipette to the cells using the micromanipulator.
2. Puncture the target cell when the tip is close enough to touch the cell membrane, and apply a small hyperpolarizing pulse to introduce the LY into the cell. The applied voltage will depend on the net charge of dye to be injected.  Alternatively, some other dyes could be used with this technique as shown in Table 1.
   Note: In principle any hydrophilic dye with MW less than 1KDa could be used. However, the rate of transfer could vary according to the weight and hydrophilicity. Additionally, unspecific transfer of the dye used must be evaluated.  
3. Capture cell images 3 min after dye injection or make a small movie with time lapse microscopy (30 fps).
   NOTE: A similar approach could be seen in Hitomi et al (2015)²⁰. To avoid communication by intercellular bridges (incomplete mitosis), a co-injection of rhodamin dextran (from 2 to 10 KDa), which does not pass through gap junctions but passes through intercellular bridges and certain types of nanotubules is recommended as shown in Figure 2.

Results

Thymic epithelial cell line IT-76MI were used to evaluate dye coupling by gap junctions as these cells were described to express functional gap junctions formed by connexin 43²¹. Figure 1 shows the injection of Lucifer Yellow when applied in the one cell below the tip of the pipette. After few minutes, connected cells become fluorescent (asterisks) indicating the diffusion of the fluorescent dye through the gap junctions. The number of cells and time to became fluo...

Discussion

In order to verify the presence of functional intercellular gap junction, the use of tracers, which are membrane impermeable, although permeable by intercellular channels are required¹⁶. Fluorescein, the first fluorescent dye to observe cell-to-cell coupling²², is permeable between non junctional membranes³ and has therefore been substituted by Lucifer Yellow dye¹⁵. Currently, to find the best choice among the many different t...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Lucifer yellow	Sigma	L0259
Lithium Chloride	Sigma	L4408
PBS tablets	Sigma	P4417
RPMI	Sigma	R4130
Bovine fetal serum	Cultilab
Trypsin	Sigma	T4799
vibration-insulated table	Newport	VH3036W-OPT	A vibration-insulated table is needed to protect the experiments from vibration and avoid cell damage
Micromanipulator	Narishige	MMO-203	This equipment allows precision adjustments of the micropipette, which is needed for cell micro injection.
Current Generator	Digitimer	DS2	To produce the dye flow through the micropipette, a current below one nano ampere was given using a current generator with an electrode inside the micropipette or an amplifier which has a capacitance compensation circuit (old electrometer) or current injection functions of new patch clamp amplifiers, and the ground wire submersed in the plate dish. Alternatively, the dye can be injected by a pneumatic microinjector, following the factory recommendations.