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Characterization of Immune Cells in Human Adipose Tissue by Using Flow Cytometry
Published on: March 6, 2018
B Lymphocytes in the Adipose Tissue Microenvironment: Multifaceted Roles in Inflammation and Metabolic Dysfunction
1Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Immunology
|July 27, 2026
Summary
Adipose tissue B cells regulate immune responses and metabolic health. Dysfunctional B cells in obesity promote inflammation and insulin resistance, while others offer protection, highlighting therapeutic potential.
Area of Science:
- Immunometabolism
- Adipose tissue biology
- B cell immunology
Background:
- Adipose tissue (AT) is an immunometabolic organ crucial for homeostasis.
- Immune cells within AT, especially B lymphocytes, significantly influence tissue function.
- Obesity and aging trigger immune remodeling in AT, impacting metabolic health.
Purpose of the Study:
- To review the development, localization, and function of AT-resident B cells.
- To examine adipocyte-B cell crosstalk mechanisms.
- To discuss the role of B cells in metabolic inflammation and potential therapeutic strategies.
Main Methods:
- Literature review of current knowledge on AT-resident B cells.
- Analysis of molecular mechanisms in adipocyte-B cell interactions.
- Discussion of dysregulation in metabolic disease and therapeutic targets.
Main Results:
- Distinct B cell subsets in AT have varied roles, from promoting inflammation (B-2, age-associated B cells) to exerting protective effects (regulatory B cells, B-1 cells).
- Adipocyte-B cell crosstalk involves adipokines, chemokines, antigen presentation, and inflammasomes.
- Dysregulated crosstalk contributes to metabolic inflammation, autoimmunity, and AT remodeling.
Conclusions:
- B cells are key players in AT immunometabolism, with specific subsets driving or mitigating inflammation.
- Understanding adipocyte-B cell interactions is vital for addressing obesity-associated metabolic diseases.
- Targeting B cell pathways offers promising therapeutic avenues for metabolic disorders.
Keywords:
B celladaptive immunityagingdamage‐associated molecular patterns (DAMPs)diabetesinflammasomeinnate immunityobesityMore Related Videos
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