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Here, we describe the isolation, culture, and adipogenic induction of stromal vascular fraction-derived preadipocytes from mouse periaortic adipose tissue, allowing for the study of perivascular adipose tissue function and its relationship with vascular cells.
Perivascular adipose tissue (PVAT) is an adipose tissue depot that surrounds blood vessels and exhibits the phenotypes of white, beige, and brown adipocytes. Recent discoveries have shed light on the central role of PVAT in regulating vascular homeostasis and participating in the pathogenesis of cardiovascular diseases. A comprehensive understanding of PVAT properties and regulation is of great importance for the development of future therapies. Primary cultures of periaortic adipocytes are valuable for studying PVAT function and the crosstalk between periaortic adipocytes and vascular cells. This paper presents an economical and feasible protocol for the isolation, culture, and adipogenic induction of stromal vascular fraction-derived preadipocytes from mouse periaortic adipose tissue, which can be useful for modeling adipogenesis or lipogenesis in vitro. The protocol outlines tissue processing and cell differentiation for culturing periaortic adipocytes from young mice. This protocol will provide the technological cornerstone at the bench side for the investigation of PVAT function.
Perivascular adipose tissue (PVAT), a perivascular structure composed of a mixture of mature adipocytes and a stromal vascular fraction (SVF), is believed to interact with the adjacent vessel wall via its secretome paracrineally1. As a critical regulator of vascular homeostasis, PVAT dysfunction is implicated in the pathogenesis of cardiovascular diseases2,3,4. The SVF of adipocyte tissue consists of several expected cell populations, including endothelial cells, immune cells, mesothelium cells, neuronal cells, and adipose stem and progenitor cells (AS....
The animal protocols were approved by the Institutional Animal Care and Use Committee at Shanghai Chest Hospital affiliated to Shanghai Jiao Tong University School of Medicine (approval number: KS23010) and were in compliance with relevant ethical regulations. Male and female C57BL/6 mice aged 4-8 weeks are to be preferred for this experiment.
1. Preparation of surgical tools, buffers, and culture media
Using this protocol described above, we carefully isolated PVATs surrounding mouse thoracic aortas (Figure 1A-D). After washing and mincing the PVATs into small pieces using sterile scissors (Figure 1E,F), tissue fragments were digested in a digestion solution containing type 1 collagenase (1 mg/mL) and dispase II (4 mg/mL) and incubated at 37 °C on a shaker for 30-45 min (Figure 1G
We propose a practical and feasible approach for the isolation and adipogenic induction of SVF-derived preadipocytes from mouse periaortic adipose tissue. The advantages of this protocol are that it is simple and economical. Adequate numbers of mice are critical for successful isolation, as insufficient tissue can result in low SVF density and poor growth state, ultimately affecting lipogenic efficiency. Additionally, mouse age is an important factor to consider as the adipogenic potential of SVF decreases with age. Rapi.......
This work was supported by the National Natural Science Foundation of China (82130012 and 81830010) and the Nurture projects for basic research of Shanghai Chest Hospital (Grant Number: 2022YNJCQ03).
....Name | Company | Catalog Number | Comments |
0.2 μm syringe filters | PALL | 4612 | |
12-well plate | Labselect | 11210 | |
15 mL centrifuge tube | Labserv | 310109003 | |
3,3',5-triiodo-L-thyronine (T3) | Sigma-Aldrich | T-2877 | 1 nM |
50 mL centrifuge tube | Labselect | CT-002-50A | |
anti-adiponectin | Abcam | ab22554 | 1:1,000 working concentration |
anti-COX IV | CST | 4850 | 1:1,000 working concentration |
anti-FABP4 | CST | 2120 | 1:1,000 working concentration |
anti-PGC1α | Abcam | ab191838 | 1:1,000 working concentration |
anti-PPARγ | Invitrogen | MA5-14889 | 1:1,000 working concentration |
anti-UCP1 | Abcam | ab10983 | 1:1,000 working concentration |
anti-α-Actinin | CST | 6487 | 1:1,000 working concentration |
BSA | Beyotime | ST023-200g | 1% |
C57BL/6 mice aged 4-8 weeks of both sexes | Shanghai Model Organisms Center, Inc. | ||
Cell Strainer 70 µm, nylon | Falcon | 352350 | |
Collagen from calf skin | Sigma-Aldrich | C8919 | |
Collagenase, Type 1 | Worthington | LS004196 | 1 mg/mL |
Dexamethasone | Sigma-Aldrich | D1756 | 1 μM |
Dispase II | Sigma-Aldrich | D4693-1G | 4 mg/mL |
Fetal bovine serum | Gibco | 16000-044 | 10% |
HEPES | Sigma-Aldrich | H4034-25G | 20 mM |
High glucose DMEM | Hyclone | SH30022.01 | |
IBMX | Sigma-Aldrich | I7018 | 0.5 mM |
Incubator with orbital shaker | Shanghai longyue Instrument Eruipment Co.,Ltd. | LYZ-103B | |
Insulin (cattle) | Sigma-Aldrich | 11070-73-8 | 1 μM |
Isoflurane | RWD | R510-22-10 | |
Krebs-Ringer's Solution | Pricella | PB180347 | protect from light |
Microsurgical forceps | Beyotime | FS233 | |
Microsurgical scissor | Beyotime | FS217 | |
Oil Red O | Sangon Biotech (Shanghai) Co., Ltd | A600395-0050 | |
PBS (Phosphate-buffered saline) | Sangon Biotech (Shanghai) Co., Ltd | B548117-0500 | |
Penicillin-Streptomycin | Gibco | 15140122 | |
Peroxidase AffiniPure Goat Anti-Mouse IgG (H+L) | Jackson ImmunoResearch | 115-035-146 | 1:5,000 working concentration |
Peroxidase AffiniPure Goat Anti-Rabbit IgG (H+L) | Jackson ImmunoResearch | 111-035-144 | 1:5,000 working concentration |
Rosiglitazone | Sigma-Aldrich | R2408 | 1 μM |
Standard forceps | Beyotime | FS225 | |
Surgical scissor | Beyotime | FS001 |
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