Salivary gland morphogenesis: possible involvement of collagenase.

T Hayakawa, J Kishi, Y Nakanishi
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Abstract

When 12-day rudiments of mouse submandibular glands were cultured, they formed an average two clefts within 24 h. The average number of the clefts, however, increased up to five in the presence of bovine tissue inhibitor of metalloproteinases (TIMP). Contrary to this, either bacterial or bovine interstitial collagenase in the medium completely inhibited the cleft formation of the glands. Electron microscopic observations revealed that the amounts of collagen bundles at the cleft points significantly increased with TIMP, but decreased with bacterial collagenase. These results strongly support the idea that endogenous collagenase regulates the cleft formation through the modulation of fibrillar architectures containing collagen in the extracellular matrix. Recently, our immunohistochemical studies clarified that collagen III, known to be rich in embryonic tissue, accumulated preferentially at the cleft points of the epithelium, and may play a crucial role in submandibular gland morphogenesis.

唾液腺形态发生:可能与胶原酶有关。
小鼠颌下腺胚培养12 d后,在24 h内平均形成2个裂口。然而,在牛组织金属蛋白酶抑制剂(TIMP)的作用下,平均裂口数量增加到5个。与此相反,培养基中的细菌或牛间质胶原酶完全抑制腺体的裂口形成。电镜观察显示,胶原束的数量在裂口点显著增加TIMP,但减少细菌胶原酶。这些结果有力地支持了内源性胶原酶通过调节细胞外基质中含有胶原的纤维结构来调节裂缝形成的观点。最近,我们的免疫组织化学研究表明,已知在胚胎组织中丰富的III型胶原蛋白优先在上皮的裂隙点积累,并可能在颌下腺形态发生中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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