BMP growth factor signaling in a biomechanical context

被引:71
作者
Kopf, Jessica [1 ]
Paarmann, Pia [1 ]
Hiepen, Christian [1 ]
Horbelt, Daniel [1 ]
Knaus, Petra [1 ]
机构
[1] Free Univ Berlin, Inst Chem Biochem, Berlin, Germany
关键词
BMP signaling; mechanotransduction; cytoskeleton; Smad; BONE MORPHOGENETIC PROTEIN; FACTOR-BETA SUPERFAMILY; STEM-CELL DIFFERENTIATION; NUCLEAR-MEMBRANE PROTEIN; TGF-BETA; SHEAR-STRESS; ENDOTHELIAL-CELLS; GENE-EXPRESSION; OSTEOGENIC DIFFERENTIATION; RECEPTOR OLIGOMERIZATION;
D O I
10.1002/biof.1137
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Bone Morphogenetic Proteins (BMPs) are members of the transforming growth factor- superfamily of secreted polypeptide growth factors and are important regulators in a multitude of cellular processes. To ensure the precise and balanced propagation of their pleiotropic signaling responses, BMPs and their corresponding signaling pathways are subject to tight control. A large variety of regulatory mechanisms throughout different biological levels combines into a complex network and provides the basis for physiological BMP function. This regulatory network not only includes biochemical factors but also mechanical cues. Both BMP signaling and mechanotransduction pathways are tightly interconnected and represent an elaborate signaling network active during development but also during organ homeostasis. Moreover, its dysregulation is associated with a number of human pathologies. A more detailed understanding of this crosstalk in respect to molecular interactions will be indispensable in the future, in particular to understand BMP-related diseases as well as with regard to an efficient clinical application of BMP ligands. (c) 2013 BioFactors, 40(2):171-187, 2014
引用
收藏
页码:171 / 187
页数:17
相关论文
共 195 条
[1]
A Large Bioactive BMP Ligand with Distinct Signaling Properties Is Produced by Alternative Proconvertase Processing [J].
Akiyama, Takuya ;
Marques, Guillermo ;
Wharton, Kristi A. .
SCIENCE SIGNALING, 2012, 5 (218)
[2]
Nuclear CDKs Drive Smad Transcriptional Activation and Turnover in BMP and TGF-β Pathways [J].
Alarcon, Claudio ;
Zaromytidou, Alexia-Ileana ;
Xi, Qiaoran ;
Gao, Sheng ;
Yu, Jianzhong ;
Fujisawa, Sho ;
Barlas, Afsar ;
Miller, Alexandria N. ;
Manova-Todorova, Katia ;
Macias, Maria J. ;
Sapkota, Gopal ;
Pan, Duojia ;
Massague, Joan .
CELL, 2009, 139 (04) :757-769
[3]
BMP-3 and BMP-6 structures illuminate the nature of binding specificity with receptors [J].
Allendorph, George P. ;
Isaacs, Michael J. ;
Kawakami, Yasuhiko ;
Belmonte, Juan Carlos Izpisua ;
Choe, Senyon .
BIOCHEMISTRY, 2007, 46 (43) :12238-12247
[4]
Bridging membrane and cytoskeleton dynamics in the secretory and endocytic pathways [J].
Anitei, Mihaela ;
Hoflack, Bernard .
NATURE CELL BIOLOGY, 2012, 14 (01) :11-19
[5]
Spatial Restriction of Bone Morphogenetic Protein Signaling in Mouse Gastrula through the mVam2-Dependent Endocytic Pathway [J].
Aoyama, Minako ;
Sun-Wada, Ge-Hong ;
Yamamoto, Akitsugu ;
Yamamoto, Masamichi ;
Hamada, Hiroshi ;
Wada, Yoh .
DEVELOPMENTAL CELL, 2012, 22 (06) :1163-1175
[6]
A Smad action turnover switch operated by WW domain readers of a phosphoserine code [J].
Aragon, Eric ;
Goerner, Nina ;
Zaromytidou, Alexia-Ileana ;
Xi, Qiaoran ;
Escobedo, Albert ;
Massague, Joan ;
Macias, Maria J. .
GENES & DEVELOPMENT, 2011, 25 (12) :1275-1288
[7]
Reduced expression of BMP-3 due to mechanical loading -: A link between mechanical stimuli and tissue differentiation [J].
Aspenberg, P ;
Basic, N ;
Tägil, M ;
Vukicevic, S .
ACTA ORTHOPAEDICA SCANDINAVICA, 2000, 71 (06) :558-562
[8]
Mechanics and mechano-biology of fracture healing in normal and osteoporotic bone [J].
Augat, Peter ;
Simon, Ulrich ;
Liedert, Astrid ;
Claes, Lutz .
OSTEOPOROSIS INTERNATIONAL, 2005, 16 (Suppl 2) :S36-S43
[9]
Comparative genomic analysis of the eight-membered ring cystine knot-containing bone morphogenetic protein antagonists [J].
Avsian-Kretchmer, O ;
Hsueh, AJW .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (01) :1-12
[10]
Deconstructing the third dimension - how 3D culture microenvironments alter cellular cues [J].
Baker, Brendon M. ;
Chen, Christopher S. .
JOURNAL OF CELL SCIENCE, 2012, 125 (13) :3015-3024