A distinct cohort of progenitor cells participates in synovial Joint and articular cartilage formation during mouse limb skeletogenesis

被引:259
作者
Koyama, Eiki [1 ]
Shibukawa, Yoshihiro [2 ]
Nagayama, Motohiko [1 ]
Sugito, Hiroki [2 ]
Young, Blanche [1 ]
Yuasa, Takahito [1 ]
Okabe, Takahiro [1 ]
Ochiai, Takanaga [1 ]
Kamiya, Nobuhiko [3 ]
Rountree, Ryan B. [4 ,5 ]
Kingsley, David M. [4 ,5 ]
Iwamoto, Masahiro [1 ]
Enomoto-Iwamoto, Motomi [1 ]
Pacifici, Maurizio [1 ]
机构
[1] Thomas Jefferson Univ, Coll Med, Dept Orthopaed Surg, Philadelphia, PA 19107 USA
[2] Tokyo Dent Coll, Dept Periodontol, Chiba, Japan
[3] NIES, Mol Dev Biol Grp, Reprod & Dev Toxicol Lab, Res Triangle Pk, NC 27709 USA
[4] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, HHMI, Stanford, CA 94305 USA
关键词
synovial joint formation; interzone; limb development; articular cartilage; Gdf5; Wnt9a; signaling pathways;
D O I
10.1016/j.ydbio.2008.01.012
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The origin, roles and fate of progenitor cells forming synovial joints during limb skeletogenesis remain largely unclear. Here we produced prenatal and postnatal genetic cell fate-maps by mating ROSA-LacZ-reporter mice with mice expressing Cre-recombinase at prospective joint sites under the control of Gdf5 regulatory sequences (Gdf5-Cre). Reporter-expressing cells initially constituted the interzone, a compact mesenchymal structure representing the first overt sign of joint formation, and displayed a gradient-like distribution along the ventral-to-dorsal axis. The cells expressed genes such as Wnt9a, Erg and collagen IIA, remained predominant in the joint-forming sites over time, gave rise to articular cartilage, synovial lining and other joint tissues, but contributed little if any to underlying growth plate cartilage and shaft. To study their developmental properties more directly, we isolated the joint-forming cells from prospective autopod joint sites using a novel microsurgical procedure and tested them in vitro. The cells displayed a propensity to undergo chondrogenesis that was enhanced by treatment with exogenous rGdf5 but blocked by Wnt9a over-expression. To test roles for such Wnt-mediated anti-chondrogenic capacity in vivo, we created conditional mutants deficient in Wnt/beta-catenin signaling using Co12-Cre or Gdf5-Cre. Synovial joints did form in both mutants; however, the joints displayed a defective flat cell layer normally abutting the synovial cavity and expressed markedly reduced levels of lubricin. In sum, our data indicate that cells present at prospective joint sites and expressing Gdf5 constitute a distinct cohort of progenitor cells responsible for limb joint formation. The cells appear to be patterned along specific limb symmetry axes and rely on local signaling tools to make distinct contributions to joint formation. (C) 2008 Elsevier Inc. All rights reserved.
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页码:62 / 73
页数:12
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