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This study developed an optimized protocol for the isolation of murine mesangial cells (MCs) and their ex vivo cell culture. These cells can be passaged multiple times, frozen, revived, and cultured without compromising cell growth or protein expression.
Mesangial cells (MCs) are stromal cells located in the middle space of the glomerulus, with pivotal functions in glomerular homeostasis. Methods for isolating, purifying, and culturing glomerular MCs have been developed and optimized since the 1980s for use in biomedical research, particularly in the field of nephrology. Mice are the most frequently used experimental animal models in research on renal diseases. In this study, we developed an optimized protocol for murine MCs isolation and ex vivo cell culture. These cells can be passaged multiple times, frozen, revived, and cultured without compromising cell growth or protein expression. This optimized approach significantly reduces the study duration for researchers and enables long-term cell preservation. The necessary equipment for the procedures is easily accessible in a basic biomedical laboratory, and the procedural steps are straightforward. The acquisition of target cells requires only 2-3 weeks, a reduction of at least 1 week compared to existing methods.
The glomerulus is a network of capillaries that performs the essential task of filtering blood to form urine1. Mesangial cells (MCs) are embedded within the mesangial matrix, situated between the glomerular capillaries, and are uniquely positioned to influence glomerular dynamics through their diverse functions2. MCs play crucial roles in the glomerulus, including glomerular development, structural support for glomerular capillaries, phagocytosis, and the production of the glomerular basement membrane matrix3. The study of mesangial cells is pivotal for advancing our understanding of renal physiol....
Animal experiments complied with the ARRIVE guidelines, and all animal procedures were conducted in accordance with national legislation and the European Commission Directive (2010/63/EU). Mice were housed and maintained in pathogen-free conditions, in compliance with the requirements of the Animal Care and Use Committees of West China Hospital, Sichuan University. All experimental animal studies were approved by the Animal Care and Use Committees of West China Hospital, Sichuan University. Eight-week-old C57BL/6JGpt male mice were used for mesangial cell isolation in this assay. The details of the reagents and equipment used in this study are listed in the Ta....
This study developed an optimized protocol for murine MCs isolation and ex vivo cell culture. To our knowledge, no standard method exists for validating primary MCs ex vivo. According to previous publications, MCs are characterized by the expression of Ξ±SMA, Vimentin, and Fibronectin3,14,15. Western blot analysis was used to detect the expression levels of MCs. The MCs isolated in this study exhibited sign.......
Kidney-related diseases are highly prevalent, and mice are widely used as the primary animal model for studying these conditions due to their genetic similarity to humans and the availability of well-established disease models. Mesangial cells play a crucial role in maintaining the normal structure and function of the glomerulus by providing structural support, regulating glomerular filtration, and participating in immune responses. While various experimental techniques exist for isolating mesangial cells from humans, ra.......
The authors declare no conflicts of interest, financial or otherwise.
This work was supported by grants to Y.Z. from the National Natural Science Foundation of China (No. 82470196, No. 82070219 and No. 81870157), and the Sichuan University Faculty Start Fund.
....Name | Company | Catalog Number | Comments |
100 Β΅m Cell Strainer | Biosharp | BS-100-CS | |
100 mm Petri Dish | Sorfa | 230301 | |
15 mL Centrifuge Tube | Sorfa | 411000 | |
15 mm glass bottom cell culture dish | Sorfa | 201200 | |
180 kDa Plus Prestained Protein Marker | Vazyme | MP201-01 | |
2 mM L-glutamine | BasalMedia | S210JV | |
4% Paraformaldehyde | Biosharp | BL539A | |
40 Β΅m Cell Strainer | Biosharp | BS-40-XBS | |
50 mL Centrifuge Tube | Sorfa | 41000 | |
60 mm Petri Dish | Sorfa | 230201 | |
75% Alcohol | Knowles | 64-17-5 | |
96 Well Cell Culture Plates, TC-treated | Servicebio | CCP-96H | |
Antibiotics (10 ΞΌg/mL ceftriaxone plus 100 ΞΌg/mL gentamicin) | NCM | C100C5 | |
BCA (Bicinchoninic acid) Protein Assay kit | CWBIO | CW0014S | |
Cell Counting Kit-8 | Oriscience | CB101 | |
Confocal Microscope | FV-3000 | Olympus | |
DMSO | Sigma | D2650 | |
DMSO | Sigma | D2650 | |
Earle's Balanced Salt Solution (1x EBSS)Β | Beyotime | Β C0213 | |
Fetal Bovine Serum (FBS) | Excell | FSP500 | |
Fluorescence Cell Analyzer | Mira FLΒ | Countstar | |
Fluoromount media | Southern Biotech | 0100-01 | |
Insulin, Transferrin, Selenium Solution 100x (ITS -G) | Gibco | 41400045 | |
Inverted Fluorescence Microscope | Olympus | IX83 | |
Lysis Buffer | Adilab | PP1101 | |
One-Step PAGE Preparation Kit (10%) | Oriscience | PB102 | |
One-Step PAGE Preparation Kit (7.5%) | Oriscience | PB101 | |
PE anti-mouse CD140b Antibody | Biolegend | 323605 | |
Phosphate Buffered Saline (PBS) | Servicebio | G4202 | |
Plastic Cell Pestle | Biofil | Β CC-4090 | |
Proteinase Inhibitor Cocktail | Roche | 4693159001 | |
PVDF Membrane | Vazyme | E802-01 | |
Recombinant Human Insulin | Solarbio | 11061-68-0 | |
Roswell Park Memorial Institute (RPMI) 1640 Medium | Corning | 10-040-CV | |
SDS-PAGE Sample Loading Buffer (5x) | Servicebio | G2013 | |
Specially customized Roswell Park Memorial Institute (RPMI) 1640 Medium (D-valine instead of L-valine) | Procell | WH3923U222 | |
TBS (Tris Buffered Saline)Β | Servicebio | G0001-2L | |
Triton X-100 | Biosharp | BS084 | |
Trypsin-EDTA (0.25%) | Gibco | 25200072 | |
Tween 20 | Biosharp | BS100 | |
Type I collagenase | Solarbio | Β CB140 |
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