Development · 2011 · 209 citations · 37 references
Life SciencesCell BiologyDevelopmental BiologyMorphogenesisOrganogenesisTissue DifferentiationAdipocyte DifferentiationAdipose TissueAngiogenesisAdipocyte BiologyAdipocyte Progenitor CellsAdipogenic DifferentiationAdipose Tissue AngiogenesisAdipose Tissue Extracellular MatrixMultipotent Progenitor CellsProgenitor Cells
Adipose tissue is a specialized energy‑storage organ whose adipocyte lineage originates from mesoderm or neuroectoderm, yet the mechanisms of its development remain poorly understood. The study aimed to investigate adipose tissue development by examining postnatal epididymal adipose tissue in mice. Researchers analyzed postnatal epididymal adipose tissue in mice to trace its cellular origins and developmental dynamics. They found that epididymal adipose tissue arises from a non‑adipose structure within the first 14 postnatal days, with early progenitors lacking adipogenic capacity that acquire it through cell‑matrix and cell‑cell interactions, and that impaired angiogenesis via VEGFA blockade or macrophage depletion disrupts development, underscoring the necessity of proper cellular, matrix, and vascular interactions.
Adipose tissue is a structure highly specialized in energy storage. The adipocyte is the parenchymal component of adipose tissue and is known to be mesoderm or neuroectoderm in origin; however, adipocyte development remains poorly understood. Here, we investigated the development of adipose tissue by analyzing postnatal epididymal adipose tissue (EAT) in mouse. EAT was found to be generated from non-adipose structure during the first 14 postnatal days. From postnatal day 1 (P1) to P4, EAT is composed of multipotent progenitor cells that lack adipogenic differentiation capacity in vitro, and can be regarded as being in the 'undetermined' state. However, the progenitor cells isolated from P4 EAT obtain their adipogenic differentiation capacity by physical interaction generated by cell-to-matrix and cell-to-cell contact both in vitro and in vivo. In addition, we show that impaired angiogenesis caused by either VEGFA blockade or macrophage depletion in postnatal mice interferes with adipose tissue development. We conclude that appropriate interaction between the cellular and matrix components along with proper angiogenesis are mandatory for the development of adipose tissue.
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Life Sciences, Endocrinology, Aging +12