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Characterization of Immune Cells in Human Adipose Tissue by Using Flow Cytometry
Published on: March 6, 2018
Innate immunity and adipose tissue biology
Andreas Schäffler1, Jürgen Schölmerich
1Department of Internal Medicine I, University Hospital of Regensburg, D-93042 Regensburg, Germany. andreas.schaeffler@klinik.uni-regensburg.de
Trends in Immunology
|May 4, 2010
Summary
Adipose tissue is an active endocrine and immune organ. Toll-like receptors (TLRs) in fat cells and macrophages link immunity and metabolism, driving inflammation in obesity.
Area of Science:
- Immunology
- Endocrinology
- Metabolism
Background:
- Adipose tissue's role has evolved from lipid storage to an endocrine and immunologically active function.
- Innate immunity mechanisms within adipose tissue are increasingly recognized.
- Toll-like receptors (TLRs) are key players in this immune activity.
Purpose of the Study:
- To review the evidence for adipose tissue's role in innate immunity.
- To focus on Toll-like receptors (TLRs) in adipocytes and adipose tissue macrophages.
- To explore the connection between innate immunity and metabolism via adipose tissue.
Main Methods:
- Review of existing scientific literature on adipose tissue, innate immunity, and Toll-like receptors.
- Analysis of studies focusing on TLR expression and function in adipocytes.
- Examination of the role and interactions of adipose tissue macrophages.
Main Results:
- Adipose tissue functions as an endocrine and immunologically active organ.
- Toll-like receptors (TLRs) are expressed and functional in adipocytes.
- Dual activation of TLR4 by lipopolysaccharide and fatty acids links innate immunity and metabolism.
- Obesity leads to macrophage infiltration and crosstalk in visceral adipose tissue, promoting inflammation.
Conclusions:
- Adipose tissue plays a critical role in innate immunity.
- The interplay between adipocytes and macrophages, particularly via TLRs, influences metabolic and immune homeostasis.
- Understanding these interactions is crucial for addressing obesity-related inflammation.
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