The pivotal role of PDGF and its receptor isoforms in adipose-derived stem cells

被引:25
作者
Kim, Won-Serk [1 ]
Park, Hyoung-Sook [2 ]
Sung, Jong-Hyuk [2 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Dermatol, Seoul, South Korea
[2] Yonsei Univ, Coll Pharm, Inchon, South Korea
基金
新加坡国家研究基金会;
关键词
Adipose-derived stem cells; Platelet-derived growth factor; Receptor; Reactive oxygen species; Mitogenic effect; GROWTH-FACTOR PDGF; IN-VITRO; TISSUE; PROLIFERATION; BB; VIVO; DIFFERENTIATION; ANGIOGENESIS; GENERATION; MIGRATION;
D O I
10.14670/HH-11-598
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Platelet-derived growth factor (PDGF) is one of the growth factors that reportedly regulates cell growth and division of mesenchymal cells. Although PDGF isoforms and their receptors reportedly play a pivotal role in mesenchymal stem cell regulation, there is a paucity of literature reviewing the role of PDGF in adipose-derived stem cells (ASCs). Therefore, we summarized previous reports on the expression and functional roles of PDGF and its receptor isoforms in this review. In addition, we examined findings pertaining to underlying molecular mechanisms and signaling pathways with special focus on PDGF-D/PDGFR beta. ASCs only express PDGF-A, -C, -D, PDGFR alpha, and PDGFR beta. PDGFRa expression decreases with adipocyte lineage, while PDGFR beta inhibits white adipocyte differentiation. In addition, PDGFR beta induces proliferation, migration, and angiogenesis and up-regulates the expression of paracrine factors in ASCs. Although PDGF-B and -D mediate their functions mainly by PDGFR beta and ROS generation, there are many differences between them in terms of regulating ASCs. PDGF-D is endogenous, generates ROS via the mitochondrial electron transport system, and regulates the autocrine loop of ASCs in vivo. Furthermore, PDGF-D has stronger mitogenic effects than PDGF-B.
引用
收藏
页码:793 / 799
页数:7
相关论文
共 47 条
[1]
Role of platelet-derived growth factors in physiology and medicine [J].
Andrae, Johanna ;
Gallini, Radiosa ;
Betsholtz, Christer .
GENES & DEVELOPMENT, 2008, 22 (10) :1276-1312
[2]
Anti-adipogenic effect of PDGF is reversed by PKC inhibition [J].
Artemenko, Y ;
Gagnon, A ;
Aubin, D ;
Sorisky, A .
JOURNAL OF CELLULAR PHYSIOLOGY, 2005, 204 (02) :646-653
[3]
In vitro migration capacity of human adipose tissue-derived mesenchymal stem cells reflects their expression of receptors for chemokines and growth factors [J].
Baek, Sun Jin ;
Kang, Sung Keun ;
Ra, Jeong Chan .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2011, 43 (10) :596-603
[4]
PDGF-BB MODULATES ENDOTHELIAL PROLIFERATION AND ANGIOGENESIS IN-VITRO VIA PDGF BETA-RECEPTORS [J].
BATTEGAY, EJ ;
RUPP, J ;
IRUELAARISPE, L ;
SAGE, EH ;
PECH, M .
JOURNAL OF CELL BIOLOGY, 1994, 125 (04) :917-928
[5]
Characterization of the adipocyte cellular lineage in vivo [J].
Berry, Ryan ;
Rodeheffer, Matthew S. .
NATURE CELL BIOLOGY, 2013, 15 (03) :302-308
[6]
REGULATION OF DNA-SYNTHESIS IN CHICKEN ADIPOCYTE PRECURSOR CELLS BY INSULIN-LIKE GROWTH-FACTORS, PLATELET-DERIVED GROWTH-FACTOR AND TRANSFORMING GROWTH-FACTOR-BETA [J].
BUTTERWITH, SC ;
GODDARD, C .
JOURNAL OF ENDOCRINOLOGY, 1991, 131 (02) :203-209
[7]
Adipose stem cells originate from perivascular cells [J].
Cai, Xiaoxiao ;
Lin, Yunfeng ;
Hauschka, Peter V. ;
Grottkau, Brian E. .
BIOLOGY OF THE CELL, 2011, 103 (09) :435-447
[8]
Platelet-derived growth-factor-releasing aligned collagen-nanoparticle fibers promote the proliferation and tenogenic differentiation of adipose-derived stem cells [J].
Cheng, XingGuo ;
Tsao, Christopher ;
Sylvia, Victor L. ;
Cornet, Douglas ;
Nicolella, Daniel P. ;
Bredbenner, Todd L. ;
Christy, Robert J. .
ACTA BIOMATERIALIA, 2014, 10 (03) :1360-1369
[9]
PDGF receptor signaling networks in normal and cancer cells [J].
Demoulin, Jean-Baptiste ;
Essaghir, Ahmed .
CYTOKINE & GROWTH FACTOR REVIEWS, 2014, 25 (03) :273-283
[10]
Epithelial-mesenchymal transition in breast cancer lines is mediated through PDGF-D released by tissue-resident stem cells [J].
Devarajan, Eswaran ;
Song, Yao-Hua ;
Krishnappa, Srinivasalu ;
Alt, Eckhard .
INTERNATIONAL JOURNAL OF CANCER, 2012, 131 (05) :1023-1031