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Fat-bone interaction within the bone marrow milieu: Impact on hematopoiesis and systemic energy metabolism

期刊

BONE
卷 119, 期 -, 页码 57-64

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bone.2018.03.012

关键词

Bone marrow milieu; Bone marrow adipose tissue; White adipose tissue; Hematopoeisis; Mesenchymal stem cells; Hematopoeitic stem cells; Adipocytes; Adipokines; Bone mineral density

资金

  1. NIH [K07 CA166177]

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The relationship between fat, bone and systemic metabolism is a growing area of scientific interest. Marrow adipose tissue is a well-recognized component of the bone marrow milieu and is metabolically distinct from current established subtypes of adipose tissue. Despite recent advances, the functional significance of marrow adipose tissue is still not clearly delineated. Bone and fat cells share a common mesenchymal stem cell (MSC) within the bone marrow, and hormones and transcription factors such as growth hormone, leptin, and peroxisomal proliferator-activated receptor gamma influence MSC differentiation into osteoblasts or adipocytes. MSC osteogenic potential is more vulnerable than adipogenic potential to radiation and chemotherapy, and this confers a risk for an abnormal fat-bone axis in survivors following cancer therapy and bone marrow transplantation. This review provides a summary of data from animal and human studies describing the relationship between marrow adipose tissue and hematopoiesis, bone mineral density, bone strength, and metabolic function. The significance of marrow adiposity in other metabolic disorders such as osteoporosis, diabetes mellitus, and estrogen and growth hormone deficiency are also discussed. We conclude that marrow adipose tissue is an active endocrine organ with important metabolic functions contributing to bone energy maintenance, osteogenesis, bone remodeling, and hematopoiesis. Future studies on the metabolic role of marrow adipose tissue may provide the critical insight necessary for selecting targeted therapeutic interventions to improve altered hematopoiesis and augment skeletal remodeling in cancer survivors. (C) 2018 Elsevier Inc. All rights reserved.

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