TY - JOUR
T1 - Independent stem cell lineages regulate adipose organogenesis and adipose homeostasis
AU - Jiang, Yuwei
AU - Berry, Daniel C.
AU - Tang, Wei
AU - Graff, Jonathan M.
N1 - Funding Information:
We are grateful to Dr. Luis Parada and the J.M.G. lab for use of equipment and helpful discussions. We thank Dr. Pierre Chambon for generously providing the SMA-Cre ERT2 mouse strain. This study was supported by the NIH and the National Institute of Diabetes and Digestive and Kidney Diseases grants (R01 DK066556, R01 DK064261, and R01 DK088220) to J.M.G. D.C.B. is supported by the National Heart, Blood and Lung Institute (5T32HL007360-34). Y.J. is supported by the American Heart Association (13POST14590008). J.M.G. is a cofounder and shareholder of Reata Pharmaceuticals.
Publisher Copyright:
© 2014 The Authors.
PY - 2014
Y1 - 2014
N2 - Adipose tissues have striking plasticity, highlighted by childhood and adult obesity. Using adipose lineage analyses, smooth muscle actin (SMA)-mural cell-fate mapping, and conditional PPARγ deletion to block adipocyte differentiation, we find two phases of adipocyte generation that emanate from two independent adipose progenitor compartments: developmental and adult. These two compartments are sequentially required for organ formation and maintenance. Although both developmental and adult progenitors are specified during the developmental period and express PPARγ, they have distinct microanatomical, functional, morphogenetic, and molecular profiles. Furthermore, the two compartments derive from different lineages; whereas adult adipose progenitors fate-map from an SMA+ mural lineage, developmental progenitors do not. Remarkably, the adult progenitor compartment appears to be specified earlier than the developmental cells and then enters the already developmentally formed adipose depots. Thus, two distinct cell compartments control adipose organ development and organ homeostasis, which may provide a discrete therapeutic target for childhood and adult obesity.
AB - Adipose tissues have striking plasticity, highlighted by childhood and adult obesity. Using adipose lineage analyses, smooth muscle actin (SMA)-mural cell-fate mapping, and conditional PPARγ deletion to block adipocyte differentiation, we find two phases of adipocyte generation that emanate from two independent adipose progenitor compartments: developmental and adult. These two compartments are sequentially required for organ formation and maintenance. Although both developmental and adult progenitors are specified during the developmental period and express PPARγ, they have distinct microanatomical, functional, morphogenetic, and molecular profiles. Furthermore, the two compartments derive from different lineages; whereas adult adipose progenitors fate-map from an SMA+ mural lineage, developmental progenitors do not. Remarkably, the adult progenitor compartment appears to be specified earlier than the developmental cells and then enters the already developmentally formed adipose depots. Thus, two distinct cell compartments control adipose organ development and organ homeostasis, which may provide a discrete therapeutic target for childhood and adult obesity.
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U2 - 10.1016/j.celrep.2014.09.049
DO - 10.1016/j.celrep.2014.09.049
M3 - Article
C2 - 25437556
AN - SCOPUS:84919727190
SN - 2211-1247
VL - 9
SP - 1007
EP - 1022
JO - Cell Reports
JF - Cell Reports
IS - 3
ER -