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Updated: Dec 23, 2025

Identification and Dissection of Diverse Mouse Adipose Depots
Published on: July 11, 2019
Human Bone Marrow Adipose Tissue is a Metabolically Active and Insulin-Sensitive Distinct Fat Depot
Tam T Pham1, Kaisa K Ivaska2, Jarna C Hannukainen1
1Turku PET Centre, University of Turku, Turku, Finland.
Bone marrow adipose tissue (BMAT) is insulin-sensitive and metabolically active in humans. Its insulin sensitivity is impaired in obesity and type 2 diabetes but improves after bariatric surgery.
Area of Science:
- Endocrinology
- Metabolism
- Adipose Tissue Biology
Background:
- Bone marrow adipose tissue (BMAT) is abundant in adult long bones, yet its metabolic functions remain largely uncharacterized.
- Understanding BMAT's role is crucial, especially concerning its potential involvement in metabolic diseases like obesity and type 2 diabetes (T2DM).
Purpose of the Study:
- To investigate the metabolic and molecular characteristics of human BMAT.
- To determine if BMAT is insulin-sensitive and how this sensitivity is affected by obesity and T2DM.
Main Methods:
- Positron emission tomography (PET) imaging with 2-[18F]fluoro-2-deoxy-D-glucose (FDG) was used to assess glucose uptake (GU) in BMAT.
- Molecular profiling of BMAT was conducted using quantitative RT-PCR.
- Studies included morbidly obese individuals (with and without T2DM) and healthy controls, with assessments before and after bariatric surgery for obese subjects.
Main Results:
- Insulin administration significantly enhanced glucose uptake in human BMAT.
- Femoral BMAT exhibited impaired insulin sensitivity in obese patients with T2DM compared to controls.
- Bariatric surgery led to improved insulin sensitivity in femoral BMAT of obese patients.
- Gene expression analysis indicated that BMAT possesses a molecular profile distinct from both white and brown adipose tissues.
Conclusions:
- Human BMAT is a metabolically active and insulin-sensitive fat depot.
- BMAT's distinct molecular characteristics suggest a unique role in whole-body energy metabolism.
- Dysregulation of BMAT insulin sensitivity in obesity and T2DM highlights its potential contribution to metabolic disorders.
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