Hedgehog signalling is required for perichondral osteoblast differentiation in zebrafish

被引:17
作者
Felber, Katharina [1 ]
Croucher, Peter [2 ]
Roehl, Henry H. [1 ]
机构
[1] Univ Sheffield, MRC Ctr Dev & Biomed Genet, Sheffield S10 2TN, S Yorkshire, England
[2] Univ Sheffield, Acad Unit Bone Biol, Sect Musculoskeletal Sci, Sch Med, Sheffield S10 2RX, S Yorkshire, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
Dermal bone; Perichondrium; Periosteum; Hedgehog; Osteoblast osteoprogenetor; Osteoblast; Osteoblastogenesis; Neural crest; Bone; Cranial; runx2/cbfa1/osf1/pebp2 alpha A; Osterix; INDIAN-HEDGEHOG; BONE-DEVELOPMENT; SKELETAL ELEMENTS; DANIO-RERIO; EXPRESSION; GENE; MORPHOGENESIS; LINEAGE; IHH; CHONDROGENESIS;
D O I
10.1016/j.mod.2010.11.006
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
In tetrapod long bones, Hedgehog signalling is required for osteoblast differentiation in the perichondrium. In this work we analyse skeletogenesis in zebrafish larvae treated with the Hedgehog signalling inhibitor cyclopamine. We show that cyclopamine treatment leads to the loss of perichondral ossification of two bones in the head. We find that the Hedgehog co-receptors patched1 and patched2 are expressed in regions of the perichondrium that will form bone before the onset of ossification. We also show that cyclopamine treatment strongly reduces the expression of osteoblast markers in the perichondrium and that perichondral ossification is enhanced in patched1 mutant fish. This data suggests a conserved role for Hedgehog signalling in promoting perichondral osteoblast differentiation during vertebrate skeletal development. However, unlike what is seen during long bone development, we did not observe ectopic chondrocytes in the perichondrium when Hedgehog signalling is blocked. This result may point to subtle differences between the development of the skeleton in the skull and limb. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:141 / 152
页数:12
相关论文
共 46 条
[1]
Regulation of skeletogenic differentiation in cranial dermal bone [J].
Abzhanov, Arhat ;
Rodda, Stephen J. ;
McMahon, Andrew P. ;
Tabin, Clifford J. .
DEVELOPMENT, 2007, 134 (17) :3133-3144
[2]
Expression of the PTCH1 tumor suppressor gene is regulated by alternative promoters and a single functional Gli-binding site [J].
Ågren, M ;
Kogerman, P ;
Kleman, MI ;
Wessling, M ;
Toftgård, R .
GENE, 2004, 330 :101-114
[3]
Mesenchymal stem cells in perichondrium express activated leukocyte cell adhesion molecule and participate in bone marrow formation [J].
Arai, F ;
Ohneda, O ;
Miyamoto, T ;
Zhang, XQ ;
Suda, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (12) :1549-1563
[4]
Characterization of two new zebrafish members of the hedgehog family:: Atypical expression of a zebrafish indian hedgehog gene in skeletal elements of both endochondral and dermal origins [J].
Avaron, F ;
Hoffman, L ;
Guay, D ;
Akimenko, MA .
DEVELOPMENTAL DYNAMICS, 2006, 235 (02) :478-489
[5]
BERESFORD WA, 1993, PATTERNS STRUCTURAL, V3, P69
[6]
BERESFORD WA, 1981, CHONDROID BONE SECON, pR17
[7]
Regulation of Zebrafish Skeletogenesis by ext2/dackel and papst1/pinscher [J].
Clement, Aurelie ;
Wiweger, Malgorzata ;
von der Hardt, Sophia ;
Rusch, Melissa A. ;
Selleck, Scott B. ;
Chien, Chi-Bin ;
Roehl, Henry H. .
PLOS GENETICS, 2008, 4 (07)
[8]
Colnot C, 2009, J BONE MINER RES, V24, P274, DOI [10.1359/jbmr.081003, 10.1359/JBMR.081003]
[9]
Cubbage CC, 1996, J MORPHOL, V229, P121, DOI 10.1002/(SICI)1097-4687(199608)229:2<121::AID-JMOR1>3.0.CO
[10]
2-4