Ohnishi Hiroe, Sasaki Hiroyuki, Nakamura Yoshihiko, Kato Shunichi, Ando Kiyoshi, Narimatsu Hisashi, Tachibana Kouichi
Research Center for Medical Glycoscience; National Institute of Advanced Industrial Science and Technology (AIST); Umezono, Tsukuba, Ibaraki, Japan; Health Research Institute; AIST; Nakouji, Amagasaki, Hyogo, Japan.
Department of Molecular Cell Biology, Institute of DNA Medicine, The Jikei University School of Medicine, Nishi-Shinbashi, Minato-ku, Tokyo 105, Japan.
Cell Adh Migr. 2013 Sep-Oct;7(5):426-33. doi: 10.4161/cam.25957. Epub 2013 Aug 5.
We previously reported that expression of CD43/leukosialin induces cell rounding and microvillus formation via inhibition of cell adhesion. Here, we found that CD34, a cell surface sialomucin and marker for hematopoietic progenitor cells, also inhibited cell adhesion and induced cell rounding and microvillus formation. Forced expression of CD34-induced cell rounding, microvillus formation, and phosphorylation of ezrin/radixin/moesin (ERM) proteins in HEK293T cells, while inhibiting integrin-mediated cell re-attachment. Furthermore, CD34+ blood cells and KG-1 cells, which express endogenous CD34 on their surface, were spherical in shape, surrounded by microvilli, and non-adherent to substrata. In addition, cleavage of O-sialomucin augmented integrin-mediated cell adhesion of KG-1 cells. These results suggest the involvement of CD34 in the inhibition of integrin-mediated cell adhesion and formation of the cell surface structure. The inhibitory function of CD34 in cell adhesion may affect cell shape organization via phosphorylation of ERM proteins. Cellular structures such as the spherical shape and microvilli of CD34+ cells may also contribute to regulation of cell adhesion.
我们之前报道过,CD43/白细胞涎酸蛋白的表达通过抑制细胞黏附诱导细胞变圆和微绒毛形成。在此,我们发现CD34,一种细胞表面涎酸黏蛋白及造血祖细胞标志物,同样抑制细胞黏附并诱导细胞变圆和微绒毛形成。在HEK293T细胞中,强制表达CD34会诱导细胞变圆、微绒毛形成以及埃兹蛋白/根蛋白/膜突蛋白(ERM)的磷酸化,同时抑制整合素介导的细胞重新黏附。此外,表面表达内源性CD34的CD34⁺血细胞和KG-1细胞呈球形,被微绒毛包围,且不黏附于基质。另外,O-涎酸黏蛋白的裂解增强了KG-1细胞整合素介导的细胞黏附。这些结果表明CD34参与了整合素介导的细胞黏附抑制及细胞表面结构的形成。CD34在细胞黏附中的抑制功能可能通过ERM蛋白的磷酸化影响细胞形态组织。CD34⁺细胞的球形和微绒毛等细胞结构也可能有助于细胞黏附的调节。