TY - JOUR
T1 - Transgenic overexpression of pregnancy-associated plasma protein-A in skeletal muscle of mice increases myofiber size and central nucleation in sedentary muscle and promotes muscle regeneration in the injured muscle
AU - Deb, Chandra
AU - Li, Bo
AU - Baylink, David J.
AU - Xing, Weirong
AU - Zhang, Wenyi
AU - Chen, Michael
AU - Wergedal, Jon E.
AU - Mohan, Subburaman
AU - Qin, Xuezhong
N1 - Copyright © 2012. Published by Elsevier Ltd.
PY - 2012/10
Y1 - 2012/10
N2 - Objective: While there is compelling evidence for an anabolic role of PAPP-A, an IGFBP protease, in muscle development, its effect on dynamic regulation of muscle regeneration has not been investigated. In this study, we evaluated the effect of transgenic PAPP-A overexpression in skeletal muscle of mice on myofiber formation in intact and crush-injured tibialus anterior muscle. Design: Skeletal muscle in transgenic mice overexpressing human PAPP-A in skeletal muscle was subjected to crush-injury. Myofiber formation and myogenic gene expression were then evaluated in injured or intact muscle of PAPP-A transgenic mice and wild-type mice. Results: In the intact muscle, aging PAPP-A transgenic (Tg.) mice (age of 12. months) showed more than a 2-fold increase in both myofiber size and number of nuclei per myofiber compared with their wild-type (Wt.) littermates. Myofibers with centered nuclei, a hallmark of muscle regeneration, were increased from < 1% in Wt. mice to 65% in Tg. muscle. In the injured muscle, reduced inflammatory cell infiltration and increased new myofiber size and the area occupied by new myofibers were observed in PAPP-A transgenic mice compared to wild-type littermates. MyoD and creatine kinase in the injured muscle was also significantly increased in the Tg. mice. Although TNF-α induced PAPP-A expression in skeletal myoblast culture and its expression increased upon injury, abrogation of TNF-α signaling in TNF-α receptor knockout mice had no impact on the extent of injury induction of PAPP-A. We also found that TGF-β expression was significantly increased following muscle injury in vivo and treatment with recombinant TGF-β in vitro significantly enhanced PAPP-A expression in skeletal myoblasts. Conclusion: Our findings demonstrate that exogenous PAPP-A can promote recovery of muscle injury in aging mice albeit the expression of endogenous PAPP-A had already been increased dramatically upon muscle injury. © 2012.
AB - Objective: While there is compelling evidence for an anabolic role of PAPP-A, an IGFBP protease, in muscle development, its effect on dynamic regulation of muscle regeneration has not been investigated. In this study, we evaluated the effect of transgenic PAPP-A overexpression in skeletal muscle of mice on myofiber formation in intact and crush-injured tibialus anterior muscle. Design: Skeletal muscle in transgenic mice overexpressing human PAPP-A in skeletal muscle was subjected to crush-injury. Myofiber formation and myogenic gene expression were then evaluated in injured or intact muscle of PAPP-A transgenic mice and wild-type mice. Results: In the intact muscle, aging PAPP-A transgenic (Tg.) mice (age of 12. months) showed more than a 2-fold increase in both myofiber size and number of nuclei per myofiber compared with their wild-type (Wt.) littermates. Myofibers with centered nuclei, a hallmark of muscle regeneration, were increased from < 1% in Wt. mice to 65% in Tg. muscle. In the injured muscle, reduced inflammatory cell infiltration and increased new myofiber size and the area occupied by new myofibers were observed in PAPP-A transgenic mice compared to wild-type littermates. MyoD and creatine kinase in the injured muscle was also significantly increased in the Tg. mice. Although TNF-α induced PAPP-A expression in skeletal myoblast culture and its expression increased upon injury, abrogation of TNF-α signaling in TNF-α receptor knockout mice had no impact on the extent of injury induction of PAPP-A. We also found that TGF-β expression was significantly increased following muscle injury in vivo and treatment with recombinant TGF-β in vitro significantly enhanced PAPP-A expression in skeletal myoblasts. Conclusion: Our findings demonstrate that exogenous PAPP-A can promote recovery of muscle injury in aging mice albeit the expression of endogenous PAPP-A had already been increased dramatically upon muscle injury. © 2012.
KW - IGF-I
KW - Muscle
KW - Muscle regeneration
KW - PAPP-A
KW - Pregnancy-Associated Plasma Protein-A/genetics
KW - Humans
KW - Mice, Transgenic
KW - Tumor Necrosis Factor-alpha/genetics
KW - Pregnancy
KW - Animals
KW - Regeneration/genetics
KW - Female
KW - Mice
KW - Muscle, Skeletal/physiology
UR - http://www.scopus.com/inward/record.url?scp=84865368487&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84865368487&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/2158d394-6cc2-38a5-813f-81f6d4555633/
U2 - 10.1016/j.ghir.2012.05.003
DO - 10.1016/j.ghir.2012.05.003
M3 - Article
C2 - 22709655
SN - 1096-6374
VL - 22
SP - 173
EP - 179
JO - Growth Hormone and IGF Research
JF - Growth Hormone and IGF Research
IS - 5
ER -