Kitazawa Sohei, Haraguchi Ryuma, Kohara Yukihiro, Kitazawa Riko
Department of Molecular Pathology, Ehime University Graduate School of Medicine.
Division of Diagnostic Pathology, Ehime University Hospital, Shitsukawa 454, Toon City, Ehime 562-0295, Japan.
Acta Histochem Cytochem. 2019 Aug 30;52(4):77-83. doi: 10.1267/ahc.19015. Epub 2019 Aug 10.
The interleukin (IL)-4, 1,25(OH)D and retinoic acid, increase surface expression of functional integrin αβ on murine osteoclast precursors. All three agonists stimulate transcription of the β gene, leading to increased steady-state levels of mRNA this protein. By contrast, mRNA levels of α remain unchanged. In each instance, the increase in the surface expression of the integrin results in increased migration of the cells onto an αβ substrate. Because β subunit, except platelet where β subunit conform a dimer with α, associates solely with α subunit monogamously, while promiscuous α subunit combines with various subunit, our present data support the idea that the β subunit governs the surface-expressed functional integrin complex.
白细胞介素(IL)-4、1,25(OH)D和视黄酸可增加小鼠破骨细胞前体上功能性整合素αβ的表面表达。这三种激动剂均刺激β基因的转录,导致该蛋白的mRNA稳态水平升高。相比之下,α的mRNA水平保持不变。在每种情况下,整合素表面表达的增加都会导致细胞向αβ底物迁移增加。由于β亚基(血小板中的β亚基与α形成二聚体的情况除外)仅与α亚基专一性结合,而α亚基则与多种亚基随机结合,因此我们目前的数据支持β亚基控制表面表达的功能性整合素复合物这一观点。