Adipose Natural Regulatory B Cells Negatively Control Adipose Tissue Inflammation

• DOI: 10.1016/j.cmet.2013.09.017
• Publication Date: 2013-10-24T22:39:00Z
• Authors: Satoshi Nishimura; Ichiro Manabe; Satoshi Takaki; Mika Nagasaki; Makoto Otsu; Hiroshi Yamashita; Junichi Sugita; Kotaro Yoshimura; Koji Eto; Issei Komuro; Takashi Kadowaki; Ryozo Nagai
• Keywords: 0301 basic medicine; 2. Zero hunger; 0303 health sciences; 03 medical and health sciences; Physiology; Cell Biology; Molecular Biology

Distinct B cell populations, designated regulatory B (Breg) cells, are known to restrain immune responses associated with autoimmune diseases. Additionally, obesity is known to induce local inflammation within adipose tissue that contributes to systemic metabolic abnormalities, but the underlying mechanisms that modulate adipose inflammation remain poorly understood. We identified Breg cells that produce interleukin-10 constitutively within adipose tissue. B cell-specific Il10 deletion enhanced adipose inflammation and insulin resistance in diet-induced obese mice, whereas adoptive transfer of adipose tissue Breg cells ameliorated those effects. Adipose environmental factors, including CXCL12 and free fatty acids, support Breg cell function, and Breg cell fraction and function were reduced in adipose tissue from obese mice and humans. Our findings indicate that adipose tissue Breg cells are a naturally occurring regulatory B cell subset that maintains homeostasis within adipose tissue and that Breg cell dysfunction contributes pivotally to the progression of adipose tissue inflammation in obesity.