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Review
. 2018 May:110:134-140.
doi: 10.1016/j.bone.2018.01.008. Epub 2018 Jan 16.

Development, regulation, metabolism and function of bone marrow adipose tissues

Affiliations
Review

Development, regulation, metabolism and function of bone marrow adipose tissues

Ziru Li et al. Bone. 2018 May.

Abstract

Most adipocytes exist in discrete depots throughout the body, notably in well-defined white and brown adipose tissues. However, adipocytes also reside within specialized niches, of which the most abundant is within bone marrow. Whereas bone marrow adipose tissue (BMAT) shares many properties in common with white adipose tissue, the distinct functions of BMAT are reflected by its development, regulation, protein secretion, and lipid composition. In addition to its potential role as a local energy reservoir, BMAT also secretes proteins, including adiponectin, RANK ligand, dipeptidyl peptidase-4, and stem cell factor, which contribute to local marrow niche functions and which may also influence global metabolism. The characteristics of BMAT are also distinct depending on whether marrow adipocytes are contained within yellow or red marrow, as these can be thought of as 'constitutive' and 'regulated', respectively. The rBMAT for instance can be expanded or depleted by myriad factors, including age, nutrition, endocrine status and pharmaceuticals. Herein we review the site specificity, age-related development, regulation and metabolic characteristics of BMAT under various metabolic conditions, including the functional interactions with bone and hematopoietic cells.

Keywords: BMAT; Bone; Development; Hematopoiesis; Regulation; Site specificity.

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Figures

Figure 1
Figure 1. The conversion of red to yellow marrow during aging
Throughout life, hematopoietic cells are gradually replaced by adipocytes within bone marrow. This conversion of red to yellow marrow begins early in life and generally occurs in a centripetal pattern, beginning in the distal bones. Accumulation of bone marrow adipocytes in elderly people is associated with development of osteoporosis. Original elements used in this diagram are from Servier Medical Art (http://smart.servier.com/).
Figure 2
Figure 2. Location and characteristics of mouse tibial BMAT
Tibiae from 20-week-old mice were decalcified, lipid stained with osmium tetroxide, and BMAT then detected by microcomputed tomography. H&E staining shows the histological difference between proximal rBMAT and distal cBMAT within tibiae. The properties of rBMAT and cBMAT are summarized in the table.

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