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Here, we present a protocol including mitochondrial tracing, direct co-culture procedures of mesenchymal stem cells (MSCs) and retinal pigment epithelial cells (ARPE19), as well as the methods for observing and statistically analyzing tunneling nanotubes (TNT) formation and mitochondrial transfer to characterize mitochondrial exchange via TNTs between MSCs and ARPE19 cells.
Mitochondrial transfer is a normal physiological phenomenon that occurs widely among various types of cells. In the study to date, the most important pathway for mitochondrial transport is through tunneling nanotubes (TNTs). There have been many studies reporting that mesenchymal stem cells (MSCs) can transfer mitochondria to other cells by TNTs. However, few studies have demonstrated the phenomenon of bidirectional mitochondrial transfer. Here, our protocol describes an experimental approach to study the phenomenon of mitochondrial transfer between MSCs and retinal pigment epithelial cells in vitro by two mitochondrial tracing methods.
We co-cultured mito-GFP-transfected MSCs with mito-RFP-transfected ARPE19 cells (a retinal pigment epithelial cell line) for 24 h. Then, all cells were stained with phalloidin and imaged by confocal microscopy. We observed mitochondria with green fluorescence in ARPE19 cells and mitochondria with red fluorescence in MSCs, indicating that bidirectional mitochondrial transfer occurs between MSCs and ARPE19 cells. This phenomenon suggests that mitochondrial transport is a normal physiological phenomenon that also occurs between MSCs and ARPE19 cells, and mitochondrial transfer from MSCs to ARPE19 cells occurs much more frequently than vice versa. Our results indicate that MSCs can transfer mitochondria into retinal pigment epithelium, and similarly predict that MSCs can fulfill their therapeutic potential through mitochondrial transport in the retinal pigment epithelium in the future. Additionally, mitochondrial transfer from ARPE19 cells to MSCs remains to be further explored.
Mitochondria serve as the primary energy source for most cell types, with mitochondrial dysfunction particularly impacting high-energy-demanding tissues like the retina1. Metabolic alterations in the retina can trigger a bioenergetic crisis, ultimately resulting in the death of photoreceptors and/or RPE cells2. Mesenchymal stem cell (MSC)-based therapies have demonstrated efficacy in treating ocular degeneration, and one of the precise mechanisms underlying the beneficial effects of MSCs on retinal tissues may be attributed to functional mitochondrial transfer3,4....
1. Generation of MSC-mito-GFP and ARPE19-mito-RFP cell lines
The schematic diagram illustrating the direct co-culture of mesenchymal stem cells (MSC) and ARPE19 cells is depicted in Figure 1. MSCs, engineered to express mito-GFP, as the donor cells and ARPE19-mito-RFP cells with violet-labeled cytoplasmic membranes as recipient cells were co-cultured at a ratio of 1:1. Following a 24 h co-culture period, the cells were stained for phalloidin and examined using confocal microscopy. The resulting cell populations included MSC-mito-GFP cells, ARPE19-mito.......
Numerous studies have demonstrated that the phenomenon of TNT-mediated mitochondrial transfer is a prevalent physiological process in various types of tissue cells10,11,12,13. Functional mitochondrial donation from MSCs to cells with mitochondrial dysfunction exhibits strong therapeutic potential3,14,15
We thank Guangzhou CSR Biotech Co. Ltd for imaging with their commercial super-resolution microscope (HIS-SIM), data acquisition, SR image reconstruction, analysis, and discussion. This work is partly supported by the National Natural Science Foundation of China (82125007,92368206) and the Beijing Natural Science Foundation (Z200014).
....Name | Company | Catalog Number | Comments |
0.25% Trypsin-EDTA | Gibco | 25200-056 | |
4% paraformaldehyde | Solarbio | P1110 | |
6-well plate | NEST | 703001 | |
15 mL centrifuge tube | BD Falcon | 352097 | |
24-well plate | NEST | 702001 | |
ARPE19 cells | ATCC | CRL-2302 | Cell lines |
Bovine serum albumin (BSA) | Beyotime | ST025 | |
CellTrace violet | Invitrogen | C34557 | |
Cover slide | NEST | 801007 | |
DMSO | sigma | D2650 | |
DPBS | Gibco | C141905005BT | |
DMEM/F-12-GlutaMAX | Gibco | 10565-042 | |
Fetal Bovine Serum (FBS) | VivaCell | C04002-500 | |
FluorSave Reagent | Millipore | 345789 | |
MSCs | Nuwacell | RC02003 | Cell lines |
ncMission | Shownin | RP02010 | |
Pen Strep | Gibco | 15140-122 | |
pCT-Mito-GFP | SBI | CYTO102-PA-1 | Plasmid; From https://www.systembio.com/mitochondria-cyto-tracer-pct-mito-gfp-cmv |
Puromycin | MCE | HY-B1743A | |
Pipette | Axygen | TF-1000-R-S | |
Phalloidin | Invitrogen | A22287 | |
Triton X-100 | Solarbio | T8200 | |
Transwell plate | Corning | 3470 |
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