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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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....

Protocol

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

  1. Autoclave surgical tools (e.g., surgical scissors and standard.......

Representative Results

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

Discussion

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.......

Acknowledgements

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).

....

Materials

NameCompanyCatalog NumberComments
0.2 μm syringe filtersPALL4612
12-well plate Labselect11210
15 mL centrifuge tubeLabserv310109003
3,3',5-triiodo-L-thyronine (T3)Sigma-AldrichT-28771 nM
50 mL centrifuge tubeLabselectCT-002-50A
anti-adiponectinAbcamab225541:1,000 working concentration
anti-COX IVCST48501:1,000 working concentration
anti-FABP4CST21201:1,000 working concentration
anti-PGC1αAbcamab1918381:1,000 working concentration
anti-PPARγInvitrogenMA5-148891:1,000 working concentration
anti-UCP1Abcamab109831:1,000 working concentration
anti-α-ActininCST64871:1,000 working concentration
BSABeyotimeST023-200g1%
C57BL/6 mice aged 4-8 weeks of both sexesShanghai Model Organisms Center, Inc.
Cell Strainer 70 µm, nylonFalcon352350
Collagen from calf skinSigma-AldrichC8919
Collagenase, Type 1WorthingtonLS0041961 mg/mL
DexamethasoneSigma-AldrichD17561 μM
Dispase IISigma-AldrichD4693-1G4 mg/mL
Fetal bovine serum Gibco16000-04410%
HEPESSigma-AldrichH4034-25G20 mM
High glucose DMEMHycloneSH30022.01
IBMX Sigma-AldrichI70180.5 mM
Incubator with orbital shakerShanghai longyue Instrument Eruipment Co.,Ltd.LYZ-103B
Insulin (cattle) Sigma-Aldrich11070-73-81 μM
IsofluraneRWDR510-22-10
Krebs-Ringer's SolutionPricella PB180347protect from light 
Microsurgical forcepsBeyotimeFS233
Microsurgical scissorBeyotimeFS217
Oil Red O Sangon Biotech (Shanghai) Co., LtdA600395-0050
PBS (Phosphate-buffered saline)Sangon Biotech (Shanghai) Co., LtdB548117-0500
Penicillin-StreptomycinGibco15140122
Peroxidase AffiniPure Goat Anti-Mouse IgG (H+L)Jackson ImmunoResearch 115-035-1461:5,000 working concentration
Peroxidase AffiniPure Goat Anti-Rabbit IgG (H+L)Jackson ImmunoResearch 111-035-1441:5,000 working concentration
RosiglitazoneSigma-AldrichR24081 μM
Standard forcepsBeyotimeFS225
Surgical scissorBeyotimeFS001

References

  1. Akoumianakis, I., Antoniades, C. The interplay between adipose tissue and the cardiovascular system: is fat always bad. Cardiovascular Research. 113 (9), 999-1008 (2017).
  2. Huang, C. L., et al.

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Stromal Vascular FractionPreadipocytesPeriaortic Adipose TissueAdipogenesisIn VitroIsolationCulturePVAT FunctionVascular HomeostasisCardiovascular Diseases

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