Nakanishi Y, Sugiura F, Kishi J, Hayakawa T
Dev Biol. 1986 Jan;113(1):201-6. doi: 10.1016/0012-1606(86)90122-3.
A collagenase inhibitor obtained from the culture medium of bovine dental pulp markedly enhanced the cleft formation of mouse embryonic salivary gland epithelium when the inhibitor was included in the culture medium for 12-day and 13-day salivary glands. Determination of collagenase activity using [3H]collagen as substrate indicated that there was a latent collagenase activity in 12-day glands. In addition, a highly purified Clostridial collagenase freed from protease and hyaluronidase activities, strongly inhibited initiation of the cleft formation of the 12-day epithelium. Scanning electron microscopic observation showed that abundant collagen-like fibrils were seen on the epithelium in the collagenase-inhibitor-treated glands compared to those in the control. These findings suggest that during early morphogenesis tissue collagenase may regulate the cleft formation in the epithelium.
当将从牛牙髓培养基中获得的胶原酶抑制剂添加到培养12天和13天的小鼠胚胎唾液腺上皮细胞的培养基中时,它能显著增强裂隙形成。以[3H]胶原为底物测定胶原酶活性表明,12天的腺体中存在潜在的胶原酶活性。此外,一种高度纯化且无蛋白酶和透明质酸酶活性的梭菌胶原酶,能强烈抑制12天上皮细胞裂隙形成的起始。扫描电子显微镜观察显示,与对照组相比,在经胶原酶抑制剂处理的腺体的上皮细胞上可见大量胶原样纤维。这些发现表明,在早期形态发生过程中,组织胶原酶可能调节上皮细胞中的裂隙形成。