TY - JOUR
T1 - Regulation of muscle hypertrophy through granulin
T2 - Relayed communication among mesenchymal progenitors, macrophages, and satellite cells
AU - Zhang, Lidan
AU - Saito, Hayato
AU - Higashimoto, Tatsuyoshi
AU - Kaji, Takayuki
AU - Nakamura, Ayasa
AU - Iwamori, Kanako
AU - Nagano, Ryoko
AU - Motooka, Daisuke
AU - Okuzaki, Daisuke
AU - Uezumi, Akiyoshi
AU - Seno, Shigeto
AU - Fukada, So ichiro
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/4/23
Y1 - 2024/4/23
N2 - Skeletal muscles exert remarkable regenerative or adaptive capacities in response to injuries or mechanical loads. However, the cellular networks underlying muscle adaptation are poorly understood compared to those underlying muscle regeneration. We employed single-cell RNA sequencing to investigate the gene expression patterns and cellular networks activated in overloaded muscles and compared these results with those observed in regenerating muscles. The cellular composition of the 4-day overloaded muscle, when macrophage infiltration peaked, closely resembled that of the 10-day regenerating muscle. In addition to the mesenchymal progenitor-muscle satellite cell (MuSC) axis, interactome analyses or targeted depletion experiments revealed communications between mesenchymal progenitors-macrophages and macrophages-MuSCs. Furthermore, granulin, a macrophage-derived factor, inhibited MuSC differentiation, and Granulin-knockout mice exhibited blunted muscle hypertrophy due to the premature differentiation of overloaded MuSCs. These findings reveal the critical role of granulin through the relayed communications of mesenchymal progenitors, macrophages, and MuSCs in facilitating efficient muscle hypertrophy.
AB - Skeletal muscles exert remarkable regenerative or adaptive capacities in response to injuries or mechanical loads. However, the cellular networks underlying muscle adaptation are poorly understood compared to those underlying muscle regeneration. We employed single-cell RNA sequencing to investigate the gene expression patterns and cellular networks activated in overloaded muscles and compared these results with those observed in regenerating muscles. The cellular composition of the 4-day overloaded muscle, when macrophage infiltration peaked, closely resembled that of the 10-day regenerating muscle. In addition to the mesenchymal progenitor-muscle satellite cell (MuSC) axis, interactome analyses or targeted depletion experiments revealed communications between mesenchymal progenitors-macrophages and macrophages-MuSCs. Furthermore, granulin, a macrophage-derived factor, inhibited MuSC differentiation, and Granulin-knockout mice exhibited blunted muscle hypertrophy due to the premature differentiation of overloaded MuSCs. These findings reveal the critical role of granulin through the relayed communications of mesenchymal progenitors, macrophages, and MuSCs in facilitating efficient muscle hypertrophy.
KW - CP: Stem cell research
KW - granulin
KW - macrophage
KW - mesenchymal progenitor
KW - muscle satellite cell
KW - overload
KW - regeneration
UR - http://www.scopus.com/inward/record.url?scp=85189551061&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85189551061&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2024.114052
DO - 10.1016/j.celrep.2024.114052
M3 - Article
C2 - 38573860
AN - SCOPUS:85189551061
SN - 2211-1247
VL - 43
JO - Cell Reports
JF - Cell Reports
IS - 4
M1 - 114052
ER -