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. 2021 Jul 1;11:16. doi: 10.1186/s13395-021-00265-6

Table 1.

Summary of endogenous murine skeletal muscle fibro-adipogenic progenitors

Murine cell Canonical Markers Alternative markers Negative markers Localization Differentiation potential Additional comments References
Embryonic-fetal FAPs

PDGFRα

TCF7L2/TCF4

Osr1

Osr2

Hox11

Tbx3

Tbx4

Tbx5

Sca-1a

CD34a

Adam-12

Tie-2a

CD45

CD31

Ter119

α7-Integrin

Muscle-associated connective tissue and muscle interstitium Robust in vitro adipogenic and fibrogenic differentiation but low chondrogenic and no detectable osteogenic or myogenic potential. Osr1+ progenitors also give rise to embryonic fibroblast-like cells in the dermis and FABP4+ adipocytes in white fat pads Little is known about their origin, fate, gene regulation, function, stemness, and self-renewal [24]; [26]; [57];
Adult FAPs

PDGFRα

SCA-1

Hic1

CD90

Decorin (Dcn)

PDGFRβb

Col1a1b

TCF7L2/TCF4b

CD34b

Adam-12c

Tie-2c

Gli1d

CD45

CD31

Ter119

α7-Integrin

NG2/Cspg4

Rsg5

Fascia, epimysium, perimysium, and endomysium; abundant as perivascular cells Adipocytes, myofibroblasts, osteocytes, and chondrocytes after muscle injury and in vitro, with no myogenic potential Required for adult skeletal muscle regeneration and homeostasis; cellular and molecular dysfunction in pathology and disease [11, 12, 27, 28]; [1]; [13]; [58]; [14]; [58]; [59]; [60]; [61]; [62], [2, 15, 53, 63, 64];

aThese markers have not been studied in the embryo with detail

bThese markers are also expressed by different cell types, including satellite cells, pericytes, and endothelial cells

cAdam-12 and Tie-2 expression appears to be restricted for a subpopulation of FAPs

dGli1 defines a subpopulation of murine muscle FAPs with pro-myogenic and anti-adipogenic functions [65]