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特定的转化生长因子-β亚型调节胚胎期小鼠的梅克尔软骨和牙齿发育。

Specific transforming growth factor-beta subtypes regulate embryonic mouse Meckel's cartilage and tooth development.

作者信息

Chai Y, Mah A, Crohin C, Groff S, Bringas P, Le T, Santos V, Slavkin H C

机构信息

Center for Craniofacial Molecular Biology, School of Dentistry, University of Southern California, Los Angeles 90033.

出版信息

Dev Biol. 1994 Mar;162(1):85-103. doi: 10.1006/dbio.1994.1069.

Abstract

Members of the transforming growth factor-beta (TGF-beta) superfamily have emerged as critical regulators for cell growth and differentiation. Whereas the different TGF-beta subtypes are equipotent in the majority of biological assays using cell lines cultured in vitro, there are indications that in more complex systems involving epithelial-mesenchymal interactions, the TGF-beta subtypes differ in their biological activities. To test the hypothesis that TGF-beta subtypes specifically regulate either Meckel's cartilage or tooth morphogenesis, we designed experiments to compare loss of function effects of TGF-beta 1, TGF-beta 2, and TGF-beta 3 subtypes using a serumless, chemically defined medium to culture embryonic mouse E10 (42-44 somite pairs) mandibular explants. The major effect of loss of function resulting from abrogation of TGF-beta 1 using antisense treatment resulted in a 20% increase (P < 0.05) in chondrocyte number, a decrease in extracellular matrix, and dysmorphology of the rostral region of Meckel's cartilage. Exogenous TGF-beta 1 provided indistinguishable recovery to the normal phenotype. TGF-beta 2 antisense treatment produced a threefold enlargement (P < 0.05) of tooth organs and advanced their development to the cap stage. TGF-beta 2 provided recovery to the normal phenotype (e.g., reduced tooth size and development to the bud stage), whereas TGF-beta 1 or TGF-beta 3 polypeptides had no effect. TGF-beta 3 antisense treatment resulted in a reduction of approximately 15% in the length of Meckel's cartilage. We interpret these results to suggest that TGF-beta 1 functions to regulate the number of chondrogenic cells, the amount of extracellular matrix, and the rate of developmental assembly of the rostral to posterior segments in forming Meckel's cartilage. TGF-beta 2 appears to regulate tooth size and stage of development without affecting cartilage. TGF-beta 3 appears to regulate Meckel's cartilage size without altering tooth size or shape. The results are discussed in terms of the regulatory functions of the TGF-beta subtypes during embryonic craniofacial morphogenesis.

摘要

转化生长因子-β(TGF-β)超家族成员已成为细胞生长和分化的关键调节因子。尽管在大多数使用体外培养细胞系的生物学检测中,不同的TGF-β亚型具有同等效力,但有迹象表明,在涉及上皮-间充质相互作用的更复杂系统中,TGF-β亚型的生物学活性存在差异。为了验证TGF-β亚型特异性调节梅克尔软骨或牙齿形态发生的假说,我们设计了实验,使用无血清、化学成分明确的培养基培养胚胎小鼠E10(42 - 44对体节)下颌外植体,比较TGF-β 1、TGF-β 2和TGF-β 3亚型功能丧失的影响。使用反义处理消除TGF-β 1导致的功能丧失的主要影响是软骨细胞数量增加20%(P < 0.05),细胞外基质减少,以及梅克尔软骨前端区域形态异常。外源性TGF-β 1使表型恢复到正常状态,难以区分。TGF-β 2反义处理使牙齿器官增大了三倍(P < 0.05),并使其发育推进到帽状期。TGF-β 2使表型恢复到正常状态(例如,牙齿尺寸减小并发育到芽状期),而TGF-β 1或TGF-β 3多肽则没有影响。TGF-β 3反义处理导致梅克尔软骨长度减少约15%。我们对这些结果的解释是,TGF-β 1的功能是调节软骨形成细胞的数量、细胞外基质的量以及在形成梅克尔软骨过程中从前端到后端节段的发育组装速率。TGF-β 2似乎调节牙齿大小和发育阶段,而不影响软骨。TGF-β 3似乎调节梅克尔软骨大小,而不改变牙齿大小或形状。将根据TGF-β亚型在胚胎颅面形态发生过程中的调节功能来讨论这些结果。

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