Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development (Reprinted from Matrix Biology, vol 34, pgs 55-63, 2014)

被引:18
作者
Jochmann, Katja
Bachvarova, Velina
Vortkamp, Andrea
机构
[1] Univ Duisburg Essen, Fac Biol, Dept Dev Biol, D-45117 Essen, Germany
[2] Univ Duisburg Essen, Ctr Med Biotechnol, D-45117 Essen, Germany
关键词
Heparan sulfate; Osteochondroma; Chondrocyte differentiation; Endochondral ossification; Indian hedgehog; Ihh; Signaling range; Exostoses; HEREDITARY MULTIPLE EXOSTOSES; GENOTYPE-PHENOTYPE CORRELATION; NDST1; GENE-FUNCTION; INDIAN HEDGEHOG; SONIC HEDGEHOG; CHONDROCYTE PROLIFERATION; CELL-SURFACE; GROWTH-PLATE; PERIPHERAL CHONDROSARCOMA; CHONDROITIN SULFATE;
D O I
10.1016/j.matbio.2014.04.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most elements of the vertebrate skeleton are formed by endochondral ossification. This process is initiated with mesenchymal cells that condense and differentiate into chondrocytes. These undergo several steps of differentiation from proliferating into hypertrophic chondrocytes, which are subsequently replaced by bone. Chondrocyte proliferation and differentiation are tightly controlled by a complex network of signaling molecules. During recent years, it has become increasingly clear that heparan sulfate (HS) carrying proteoglycans play a critical role in controlling the distribution and activity of these secreted factors. In this review we summarize the current understanding of the role of HS in regulating bone formation. In human, mutations in the HS synthetizing enzymes Ext1 and Ext2 induce the Multiple Osteochondroma syndrome, a skeletal disorder characterized by short stature and the formation of benign cartilage-capped tumors. We review the current insight into the origin of the disease and discuss its possible molecular basis. In addition, we summarize the existing insight into the role of HS as a regulator of signal propagation and signaling strength in the developing skeleton. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:239 / 247
页数:9
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