TY - JOUR
T1 - The dorsal aortic compartment is a developmental source of brown adipose tissue in mice
AU - Heider, Sophie
AU - Fischer, Cornelius
AU - Secener, Ali Kerim
AU - Vallecillo-Garcı́a, Pedro
AU - Kotsaris, Georgios
AU - Meisen, Zarah G
AU - Pawolski, Verena
AU - Giesecke-Thiel, Claudia
AU - Conrad, Thomas
AU - Schulz, Tim J
AU - Sauer, Sascha
AU - Stricker, Sigmar
N1 - Publisher Copyright:
© The Author(s) 2026.
PY - 2026/12
Y1 - 2026/12
N2 - White adipose tissue primarily stores energy while brown adipose tissue dissipates energy as heat, holding promise for therapeutic use. Brown adipose tissue in the anterior trunk is believed to derive from the somitic mesoderm, although some depots are of partially unknown origin. Here we show that the subscapular, lateral, cervical and peri-aortic brown adipose depots, but not the interscapular depot, are in part formed by a non-somitic source. Single-cell sequencing along with genetic lineage tracing indicates that at embryonic day 9.5 the dorsal aorta compartment harbors multipotent mesenchymal progenitors expressing the transcription factor Osr1. Spreading laterally from the dorsal aortic midline, these cells contribute to adipose, cartilage and myogenic lineages. This study uncovers an alternative source of brown adipose tissue and suggests that a fraction of dorsal aorta-associated mesenchymal Osr1+ cells may represent the in vivo correlate of a multipotent progenitor cell type so far only characterized in vitro, the mesoangioblast.
AB - White adipose tissue primarily stores energy while brown adipose tissue dissipates energy as heat, holding promise for therapeutic use. Brown adipose tissue in the anterior trunk is believed to derive from the somitic mesoderm, although some depots are of partially unknown origin. Here we show that the subscapular, lateral, cervical and peri-aortic brown adipose depots, but not the interscapular depot, are in part formed by a non-somitic source. Single-cell sequencing along with genetic lineage tracing indicates that at embryonic day 9.5 the dorsal aorta compartment harbors multipotent mesenchymal progenitors expressing the transcription factor Osr1. Spreading laterally from the dorsal aortic midline, these cells contribute to adipose, cartilage and myogenic lineages. This study uncovers an alternative source of brown adipose tissue and suggests that a fraction of dorsal aorta-associated mesenchymal Osr1+ cells may represent the in vivo correlate of a multipotent progenitor cell type so far only characterized in vitro, the mesoangioblast.
KW - Animals
KW - Adipose Tissue, Brown/embryology
KW - Mice
KW - Aorta/embryology
KW - Cell Lineage
KW - Mesenchymal Stem Cells/metabolism
KW - Transcription Factors/metabolism
KW - Mice, Inbred C57BL
KW - Mesoderm/cytology
KW - Single-Cell Analysis
KW - Female
KW - Adipose Tissue, White/metabolism
KW - Male
KW - Gene Expression Regulation, Developmental
KW - Cell Differentiation
UR - https://www.scopus.com/pages/publications/105027179829
U2 - 10.1038/s41467-025-68147-9
DO - 10.1038/s41467-025-68147-9
M3 - Journal article
C2 - 41501080
SN - 2041-1723
VL - 17
SP - 286
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 286
ER -