Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice

被引:9
作者
Yang, Ling [1 ,2 ]
Gu, Shuping [2 ]
Ye, Wenduo [2 ]
Song, Yingnan [2 ,3 ]
Chen, YiPing [2 ,3 ]
机构
[1] Sun Yat Sen Univ, Guanghua Sch Stomatol, Hosp Stomatol, Guangdong Prov Key Lab Stomatol, Guangzhou 510055, Guangdong, Peoples R China
[2] Tulane Univ, Dept Cell & Mol Biol, New Orleans, LA 70118 USA
[3] Fujian Normal Univ, Southern Ctr Biomed Res, Fujian Key Lab Dev & Neural Biol, Coll Life Sci, Fuzhou 350108, Fujian, Peoples R China
关键词
Indian hedgehog; Cranial neural crest; Temporomandibular joint; Condyle; Glenoid fossa; MANDIBULAR CONDYLAR CARTILAGE; RUNX2-DEFICIENT MICE; TMJ DEVELOPMENT; MOUSE EMBRYOS; DIFFERENTIATION; EXPRESSION; MESENCHYME; RECEPTOR; PROTEIN; GROWTH;
D O I
10.1007/s00441-015-2306-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Extensive studies have pinpointed the crucial role of Indian hedgehog (Ihh) signaling in the development of the appendicular skeleton and the essential function of Ihh in the formation of the temporomandibular joint (TMJ). In this study, we have investigated the effect of augmented Ihh signaling in TMJ development. We took a transgenic gain-of-function approach by overexpressing Ihh in the cranial neural crest (CNC) cells using a conditional Ihh transgenic allele and the Wnt1-Cre allele. We found that Wnt1-Cre-mediated tissue-specific overexpression of Ihh in the CNC lineage caused severe craniofacial abnormalities, including cleft lip/palate, encephalocele, anophthalmos, micrognathia, and defective TMJ development. In the mutant TMJ, the glenoid fossa was completely absent, whereas the condyle and the articular disc appeared relatively normal with slightly delayed chondrocyte differentiation. Our findings thus demonstrate that augmented Ihh signaling is detrimental to craniofacial development, and that finely tuned Ihh signaling is critical for TMJ formation. Our results also provide additional evidence that the development of the condyle and articular disc is independent of the glenoid fossa.
引用
收藏
页码:105 / 115
页数:11
相关论文
共 39 条
  • [1] SCHEMES OF ZONATION IN MANDIBULAR CONDYLE
    BERESFORD, WA
    [J]. AMERICAN JOURNAL OF ORTHODONTICS AND DENTOFACIAL ORTHOPEDICS, 1975, 68 (02) : 189 - 195
  • [2] Chai Y, 2000, DEVELOPMENT, V127, P1671
  • [3] Isolation and Characterization of Murine Mandibular Condylar Cartilage Cell Populations
    Chen, J.
    Utreja, A.
    Kalajzic, Z.
    Sobue, T.
    Rowe, D.
    Wadhwa, S.
    [J]. CELLS TISSUES ORGANS, 2012, 195 (03) : 232 - 243
  • [4] Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
    Chiang, C
    Ying, LTT
    Lee, E
    Young, KE
    Corden, JL
    Westphal, H
    Beachy, PA
    [J]. NATURE, 1996, 383 (6599) : 407 - 413
  • [5] Early eye development in vertebrates
    Chow, RL
    Lang, RA
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2001, 17 : 255 - 296
  • [6] Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase
    Danielian, PS
    Muccino, D
    Rowitch, DH
    Michael, SK
    McMahon, AP
    [J]. CURRENT BIOLOGY, 1998, 8 (24) : 1323 - 1326
  • [7] PRENATAL DEVELOPMENT OF MANDIBULAR JOINT IN MICE
    FROMMER, J
    [J]. ANATOMICAL RECORD, 1964, 150 (04): : 449 - +
  • [8] Bone morphogenetic protein rescues the lack of secondary cartilage in Runx2-deficient mice
    Fukuoka, Hiroki
    Shibata, Shunichi
    Suda, Naoto
    Yamashita, Yasuo
    Komori, Toshihisa
    [J]. JOURNAL OF ANATOMY, 2007, 211 (01) : 8 - 15
  • [9] Shox2-deficiency leads to dysplasia and ankylosis of the temporomandibular joint in mice
    Gu, Shuping
    Wei, Na
    Yu, Ling
    Fei, Jian
    Chen, YiPing
    [J]. MECHANISMS OF DEVELOPMENT, 2008, 125 (08) : 729 - 742
  • [10] BMPRIA Mediated Signaling Is Essential for Temporomandibular Joint Development in Mice
    Gu, Shuping
    Wu, Weijie
    Liu, Chao
    Yang, Ling
    Sun, Cheng
    Ye, Wenduo
    Li, Xihai
    Chen, Jianquan
    Long, Fanxin
    Chen, YiPing
    [J]. PLOS ONE, 2014, 9 (08):