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整合素 α11β1 是胶原 XIII 的受体。

Integrin α11β1 is a receptor for collagen XIII.

机构信息

Oulu Center for Cell-Matrix Research, Faculty of Biochemistry and Molecular Medicine, University of Oulu, P.O. Box 5400, FIN-90014, Oulu, Finland.

Biocenter Oulu and Faculty of Biochemistry and Molecular Medicine, University of Oulu, P.O. Box 5000, FIN-90014, Oulu, Finland.

出版信息

Cell Tissue Res. 2021 Mar;383(3):1135-1153. doi: 10.1007/s00441-020-03300-y. Epub 2020 Dec 11.

Abstract

Collagen XIII is a conserved transmembrane collagen mainly expressed in mesenchymal tissues. Previously, we have shown that collagen XIII modulates tissue development and homeostasis. Integrins are a family of receptors that mediate signals from the environment into the cells and vice versa. Integrin α11β1 is a collagen receptor known to recognize the GFOGER (O=hydroxyproline) sequence in collagens. Interestingly, collagen XIII and integrin α11β1 both have a role in the regulation of bone homeostasis. To study whether α11β1 is a receptor for collagen XIII, we utilized C2C12 cells transfected to express α11β1 as their only collagen receptor. The interaction between collagen XIII and integrin α11β1 was also confirmed by surface plasmon resonance and pull-down assays. We discovered that integrin α11β1 mediates cell adhesion to two collagenous motifs, namely GPKGER and GF(S)QGEK, that were shown to act as the recognition sites for the integrin α11-I domain. Furthermore, we studied the in vivo significance of the α11β1-collagen XIII interaction by crossbreeding α11 null mice (Itga11) with mice overexpressing Col13a1 (Col13a1). When we evaluated the bone morphology by microcomputed tomography, Col13a1 mice had a drastic bone overgrowth followed by severe osteoporosis, whereas the double mutant mouse line showed a much milder bone phenotype. To conclude, our data identifies integrin α11β1 as a new collagen XIII receptor and demonstrates that this ligand-receptor pair has a role in the maintenance of bone homeostasis.

摘要

胶原 XIII 是一种保守的跨膜胶原,主要在间充质组织中表达。此前,我们已经表明胶原 XIII 调节组织发育和内稳态。整合素是一类受体,可将环境信号传递到细胞内,反之亦然。整合素 α11β1 是一种已知识别胶原中 GFOGER(O=羟脯氨酸)序列的胶原受体。有趣的是,胶原 XIII 和整合素 α11β1 在调节骨内稳态方面都有作用。为了研究 α11β1 是否是胶原 XIII 的受体,我们利用转染表达 α11β1 作为其唯一胶原受体的 C2C12 细胞进行研究。通过表面等离子体共振和下拉实验也证实了胶原 XIII 和整合素 α11β1 之间的相互作用。我们发现整合素 α11β1 介导细胞黏附到两个胶原基序,即 GPKGER 和 GF(S)QGEK,这两个基序被证明是整合素 α11-I 结构域的识别位点。此外,我们通过杂交α11 缺失小鼠(Itga11)和过表达 Col13a1(Col13a1)的小鼠来研究 α11β1-胶原 XIII 相互作用的体内意义。当我们通过微计算机断层扫描评估骨形态时,Col13a1 小鼠出现严重的骨过度生长,随后出现严重的骨质疏松症,而双突变小鼠系则表现出较轻的骨表型。总之,我们的数据确定整合素 α11β1 为胶原 XIII 的新受体,并表明该配体-受体对在维持骨内稳态方面具有作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c9a/7960628/613d1dfd7a46/441_2020_3300_Fig1_HTML.jpg

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