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对腹足纲软体动物皱纹盘鲍血细胞中胶原蛋白的研究以及IGF-I对其从头合成的调控

Collagen study and regulation of the de novo synthesis by IGF-I in hemocytes from the gastropod mollusc, Haliotis tuberculata.

作者信息

Serpentini A, Ghayor C, Poncet J M, Hebert V, Galéra P, Pujol J P, Boucaud-Camou E, Lebel J M

机构信息

Laboratoire de Biologie et Biotechnologies Marines, IBBA, IFREMER URM 14, Université de Caen, 14 032 Caen Cédex, France.

出版信息

J Exp Zool. 2000 Sep 1;287(4):275-84.

Abstract

To evidence a collagen synthesis and identify which type(s) of collagen is present in hemocytes from the mollusc Haliotis tuberculata, we have performed three separate approaches, namely, de novo synthesis by cultured cells, immunological approaches, and northern blot analysis. We demonstrated first that after 40-hr labeling, the de novo synthesis of collagen in the cell layer of cultured hemocytes represents 9.48 +/- 1.25% with respect to the total [(3)H]proline-labeled protein synthesis. In addition, IGF-I elicited a significant stimulation of collagen synthesis in cultured hemocytes in a dose-dependent manner from 10(-10) to 10(-8) M. The maximal stimulation (10(-9) M) induced an increase of 286 +/- 56% with respect to 100% control. By immunocytochemistry and immunoblotting, we showed that hemocytes present immunoreactive molecules to antibodies directed against the type I fibrillar collagen. In addition, using as a probe Hf 677 corresponding to a human pro alpha1(I) collagen cDNA and which encompasses the (Gly-X-Y) repeated sequence found in all Metazoa, four collagen transcripts of approximately 6.4, 5, 2.2, and 2 kb in length have been detected. These data suggest the presence of fibrillar type I collagen in hemocytes and are compatible with the concept that these cells are involved in the extracellular matrix deposition, a cardinal function in tissue repair as well as in developmental processes. Our model may appear as an excellent system to study the role of growth factors on the regulation of collagen synthesis by molluscan hemocytes. J. Exp. Zool. 287:275-284, 2000.

摘要

为了证明胶原蛋白的合成,并确定在软体动物皱纹盘鲍的血细胞中存在哪种类型的胶原蛋白,我们采用了三种不同的方法,即培养细胞的从头合成、免疫学方法和Northern印迹分析。我们首先证明,在40小时的标记后,培养血细胞的细胞层中胶原蛋白的从头合成相对于总[³H]脯氨酸标记的蛋白质合成占9.48±1.25%。此外,胰岛素样生长因子-I(IGF-I)以剂量依赖的方式从10⁻¹⁰到10⁻⁸M显著刺激培养血细胞中的胶原蛋白合成。最大刺激(10⁻⁹M)相对于100%对照诱导增加了286±56%。通过免疫细胞化学和免疫印迹,我们表明血细胞对针对I型纤维状胶原蛋白的抗体呈现免疫反应性分子。此外,使用对应于人α1(I)型原胶原cDNA的Hf 677作为探针,该探针包含在所有后生动物中发现的(Gly-X-Y)重复序列,检测到了长度约为6.4、5、2.2和2kb的四种胶原蛋白转录本。这些数据表明血细胞中存在I型纤维状胶原蛋白,并且与这些细胞参与细胞外基质沉积的概念一致,细胞外基质沉积在组织修复以及发育过程中是一项关键功能。我们的模型可能是研究生长因子对软体动物血细胞胶原蛋白合成调节作用的一个优秀系统。《实验动物学杂志》287:275 - 284,2000年。

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