TY - JOUR
T1 - Osteopontin is a myosphere-derived secretory molecule that promotes angiogenic progenitor cell proliferation through the phosphoinositide 3-kinase/Akt pathway
AU - Ogata, Takehiro
AU - Ueyama, Tomomi
AU - Nomura, Tetsuya
AU - Asada, Satoshi
AU - Tagawa, Masashi
AU - Nakamura, Tomoyuki
AU - Takahashi, Tomosaburo
AU - Matsubara, Hiroaki
AU - Oh, Hidemasa
N1 - Funding Information:
We are grateful to Ms. A. Kosugi, Ms. M. Nishikawa, and Mr. M. Kuramoto for their skillful technical assistance. This work was supported by Grants-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and by Grants-in-Aid from the Ministry of Health, Labor, and Welfare of Japan, Japan Association for the Advancement of Medical Equipment, Takeda Science Foundation, Novartis Research Award on Molecular and Cellular Cardiology, Kanae Foundation for Life & Socio-Medical Science, Suzuken Memorial Foundation, and Mochida Memorial Foundation.
PY - 2007/7/27
Y1 - 2007/7/27
N2 - We have reported that skeletal myosphere-derived progenitor cells (MDPCs) can differentiate into vascular cells, and that MDPC transplantation into cardiomyopathic hearts improves cardiac function. However, the autocrine/paracrine molecules and underlying mechanisms responsible for MDPC growth have not yet been determined. To explore the molecules enhancing the proliferation of MDPCs, we performed serial analysis of gene expression and signal sequence trap methods using RNA isolated from MDPCs. We identified osteopontin (OPN), a secretory molecule, as one of most abundant molecules expressed in MDPCs. OPN provided a proliferative effect for MDPCs. MDPCs treated with OPN showed Akt activation, and inhibition of the phosphoinositide 3-kinase (PI3K)/Akt pathway repressed the proliferative effect of OPN. Furthermore, OPN-pretreated MDPCs maintained their differentiation potential into endothelial and vascular smooth muscle cells. These findings indicate an important role of OPN as an autocrine/paracrine molecule in regulating the proliferative growth of muscle-derived angiogenic progenitor cells via the PI3K/Akt pathway.
AB - We have reported that skeletal myosphere-derived progenitor cells (MDPCs) can differentiate into vascular cells, and that MDPC transplantation into cardiomyopathic hearts improves cardiac function. However, the autocrine/paracrine molecules and underlying mechanisms responsible for MDPC growth have not yet been determined. To explore the molecules enhancing the proliferation of MDPCs, we performed serial analysis of gene expression and signal sequence trap methods using RNA isolated from MDPCs. We identified osteopontin (OPN), a secretory molecule, as one of most abundant molecules expressed in MDPCs. OPN provided a proliferative effect for MDPCs. MDPCs treated with OPN showed Akt activation, and inhibition of the phosphoinositide 3-kinase (PI3K)/Akt pathway repressed the proliferative effect of OPN. Furthermore, OPN-pretreated MDPCs maintained their differentiation potential into endothelial and vascular smooth muscle cells. These findings indicate an important role of OPN as an autocrine/paracrine molecule in regulating the proliferative growth of muscle-derived angiogenic progenitor cells via the PI3K/Akt pathway.
KW - Differentiation
KW - Osteopontin
KW - Progenitor cells
KW - Proliferation
KW - Skeletal muscle
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U2 - 10.1016/j.bbrc.2007.05.104
DO - 10.1016/j.bbrc.2007.05.104
M3 - Article
C2 - 17537408
AN - SCOPUS:34249942727
SN - 0006-291X
VL - 359
SP - 341
EP - 347
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -