The ominous triad of adipose tissue dysfunction: Inflammation, fibrosis, and impaired angiogenesis

Clair Crewe, Yu Aaron An, Philipp E. Scherer

Research output: Contribution to journalReview article

102 Citations (Scopus)

Abstract

There are three dominant contributors to the pathogenesis of dysfunctional adipose tissue (AT) in obesity: unresolved inflammation, inappropriate extracellular matrix (ECM) remodeling and insufficient angiogenic potential. The interactions of these processes during AT expansion reflect both a linear progression as well as feed-forward mechanisms. For example, both inflammation and inadequate angiogenic remodeling can drive fibrosis, which can in turn promote migration of immune cells into adipose depots and impede further angiogenesis. Therefore, the relationship between the members of this triad is complex but important for our understanding of the pathogenesis of obesity. Here we untangle some of these intricacies to highlight the contributions of inflammation, angiogenesis, and the ECM to both "healthy" and "unhealthy" AT expansion.

Original languageEnglish (US)
Pages (from-to)74-82
Number of pages9
JournalJournal of Clinical Investigation
Volume127
Issue number1
DOIs
StatePublished - Jan 3 2017

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Tissue Expansion
Adipose Tissue
Fibrosis
Inflammation
Extracellular Matrix
Obesity
Cell Movement

ASJC Scopus subject areas

  • Medicine(all)

Cite this

The ominous triad of adipose tissue dysfunction : Inflammation, fibrosis, and impaired angiogenesis. / Crewe, Clair; An, Yu Aaron; Scherer, Philipp E.

In: Journal of Clinical Investigation, Vol. 127, No. 1, 03.01.2017, p. 74-82.

Research output: Contribution to journalReview article

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