Adipose Tissue Fibrosis: Mechanisms, Models, and Importance

被引:96
作者
DeBari, Megan K. [1 ]
Abbott, Rosalyn D. [2 ]
机构
[1] Carnegie Mellon Univ, Dept Mat Sci & Engn, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Biomed Engn, Pittsburgh, PA 15213 USA
关键词
adipose tissue; fibrosis; in vitro models; in vivo models; biomaterials; MESENCHYMAL STEM-CELLS; NECROSIS-FACTOR-ALPHA; UNILOCULAR FAT-CELLS; EXTRACELLULAR-MATRIX; IN-VITRO; INSULIN-RESISTANCE; ADIPOGENIC DIFFERENTIATION; ADIPOCYTE DIFFERENTIATION; MAST-CELLS; PROINFLAMMATORY STATE;
D O I
10.3390/ijms21176030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increases in adipocyte volume and tissue mass due to obesity can result in inflammation, further dysregulation in adipose tissue function, and eventually adipose tissue fibrosis. Like other fibrotic diseases, adipose tissue fibrosis is the accumulation and increased production of extracellular matrix (ECM) proteins. Adipose tissue fibrosis has been linked to decreased insulin sensitivity, poor bariatric surgery outcomes, and difficulty in weight loss. With the rising rates of obesity, it is important to create accurate models for adipose tissue fibrosis to gain mechanistic insights and develop targeted treatments. This article discusses recent research in modeling adipose tissue fibrosis using in vivo and in vitro (2D and 3D) methods with considerations for biomaterial selections. Additionally, this article outlines the importance of adipose tissue in treating other fibrotic diseases and methods used to detect and characterize adipose tissue fibrosis.
引用
收藏
页码:1 / 24
页数:23
相关论文
共 185 条
[21]   Bariatric surgery: A systematic review and meta-analysis [J].
Buchwald, H ;
Avidor, Y ;
Braunwald, E ;
Jensen, MD ;
Pories, W ;
Fahrbach, K ;
Schoelles, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (14) :1724-1737
[22]   Adipose tissue fibrosis [J].
Buechler, Christa ;
Krautbauer, Sabrina ;
Eisinger, Kristina .
WORLD JOURNAL OF DIABETES, 2015, 6 (04) :548-553
[23]   Deconstructing Adipogenesis Induced by β3-Adrenergic Receptor Activation with Single-Cell Expression Profiling [J].
Burl, Rayanne B. ;
Ramseyer, Vanesa D. ;
Rondini, Elizabeth A. ;
Pique-Regi, Roger ;
Lee, Yun-Hee ;
Granneman, James G. .
CELL METABOLISM, 2018, 28 (02) :300-+
[24]   FAT-METABOLISM IN HUMAN OBESITY [J].
CAMPBELL, PJ ;
CARLSON, MG ;
NURJHAN, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (04) :E600-E605
[25]   Angiogenesis modulates adipogenesis and obesity [J].
Cao, Yihai .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (09) :2362-2368
[26]   Evolution of subcutaneous adipose tissue fibrosis after bariatric surgery [J].
Chabot, K. ;
Gauthier, M. -S. ;
Garneau, P. Y. ;
Rabasa-Lhoret, R. .
DIABETES & METABOLISM, 2017, 43 (02) :125-133
[27]   Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY3-36 [J].
Challis, BG ;
Coll, AP ;
Yeo, GSH ;
Pinnock, SB ;
Dickson, SL ;
Thresher, RR ;
Dixon, J ;
Zahn, D ;
Rochford, JJ ;
White, A ;
Oliver, RL ;
Millington, G ;
Aparicio, SA ;
Colledge, WH ;
Russ, AP ;
Carlton, MB ;
O'Rahilly, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (13) :4695-4700
[28]   Second harmonic generation microscopy for quantitative analysis of collagen fibrillar structure [J].
Chen, Xiyi ;
Nadiarynkh, Oleg ;
Plotnikov, Sergey ;
Campagnola, Paul J. .
NATURE PROTOCOLS, 2012, 7 (04) :654-669
[29]   miR-155 regulates differentiation of brown and beige adipocytes via a bistable circuit [J].
Chen, Yong ;
Siegel, Franziska ;
Kipschull, Stefanie ;
Haas, Bodo ;
Froehlich, Holger ;
Meister, Gunter ;
Pfeifer, Alexander .
NATURE COMMUNICATIONS, 2013, 4
[30]   Refining the adipose progenitor cell landscape in healthy and obese visceral adipose tissue using single-cell gene expression profiling [J].
Cho, Dong Seong ;
Lee, Bolim ;
Doles, Jason D. .
LIFE SCIENCE ALLIANCE, 2019, 2 (06)