Expression of p21WAF1/CIP1 during mouse odontogenesis

被引:28
作者
Bloch-Zupan, A
Leveillard, T
Gorry, P
Fausser, JL
Ruch, JV
机构
[1] Fac Med Strasbourg, Inst Med Biol, INSERM, U424, F-67085 Strasbourg, France
[2] Fac Dent, Dept Pedodont, Strasbourg, France
[3] Univ Strasbourg 1, IGBMC, Strasbourg, France
[4] Univ Bordeaux 2, Sch Med, Cell Biol Lab, F-33076 Bordeaux, France
关键词
cellular differentiation; odontogenesis; organ culture; p21; retinoic acid;
D O I
10.1111/j.1600-0722.1998.tb02160.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
p21(WAF1/CIP1) is a cyclin-dependent kinase (Cdk) inhibitor. This protein may function during development as an inducible growth inhibitor that contributes to cell cycle exit and differentiation. The expression pattern of p21 during mouse embryogenesis was correlated with terminal differentiation of multiple cell lineages including skeletal muscles, cartilage, skin and nasal epithelium. p21 expression was analyzed by in situ hybridization during odontogenesis as well as during in vitro tooth development in chemically defined medium with or without retinoic acid. p21 transcripts were detected in the restricted area of inner dental epithelium during late cap and initial bell stages and then confined to the post-mitotic odontoblasts and ameloblasts. The replicating cells were devoid of any signal. The distribution of p21 mRNA in vitro, whatever the culture conditions, was similar to the in vivo pattern. p21 protein immunolocalization was superimposed on the transcripts distribution but more restricted in ameloblasts. TGF beta 1 is known to induce p21 expression. During dental cytodifferentiations, TGF beta 1 and p21 expressions overlap. Growth inhibition by TGF beta 1 may be associated with p21 induction.
引用
收藏
页码:104 / 111
页数:8
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