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[Effect of phosphorylation of cortactin at different sites on secretion by airway mucus 5AC].
Li, Qi; Zhou, Xiangdong; Zeng, Man; Zhong, Youqing; P Kolosov, Victor; M Perelman, Juliy.
Afiliação
  • Li Q; Department of Respiratory Medicine, First Affiliated Hospital, Hainan Medical College, Haikou 570102, China.
  • Zhou X; Department of Respiratory Medicine, First Affiliated Hospital, Hainan Medical College, Haikou 570102, China.
  • Zeng M; Department of Respiratory Medicine, First Affiliated Hospital, Hainan Medical College, Haikou 570102, China.
  • Zhong Y; Department of Respiratory Medicine, First Affiliated Hospital, Hainan Medical College, Haikou 570102, China.
  • P Kolosov V; Far Eastern Scientific Center of Physiology and Pathology of Respiration, Siberian Branch, Russian Academy of Medical Sciences, Blagoveschensk 675000, Russia.
  • M Perelman J; Far Eastern Scientific Center of Physiology and Pathology of Respiration, Siberian Branch, Russian Academy of Medical Sciences, Blagoveschensk 675000, Russia.
Zhong Nan Da Xue Xue Bao Yi Xue Ban ; 44(1): 1-8, 2019 Jan 28.
Article em Zh | MEDLINE | ID: mdl-30837395
OBJECTIVE: To explore the role of cortical actin-binding protein (cortactin) in shear stress-induced mucin (MUC) 5AC secretion in human airway epithelial cells and the effect of phosphorylation of cortactin at different sites.
 Methods: HBE16 airway epithelial cells were cultured, and then transfected with mutation carrier, such as pEGFP-N1-cortactin (Cort), pEGFP-N1-Cort-Y421A, pEGFP-N1-Cort-Y470A and pEGFP-N1-Cort-Y486A. The cells were divided into a normal control group, a shear stress group, a shear stress + pEGFP-N1 group, a shear stress + PEGFP-N1-Cort group, a shear stress + pEGFP-N1-Cort-Y421A group, a shear stress + pEGFP-N1-Cort-Y470A group, and a shear stress + pEGFP-N1-Cort-Y486A group. The shear stress were set at 4 dynes/cm2. The levels of MUC5AC protein and mRNA in cells and culture supernatant were assayed with enzyme-linked immunosorbent assay (ELISA) and real-time PCR. The cortactin and phosphorylated cortactin were detected by Western blot. F-actin was stained by fluorescein isothiocyanate (FITC)-phalloidin.
 Results: There was an obvious increase of phosphorylated cortactin in cells exposed to 4 dynes/cm2 of shear stress for 30 min, which reached climax at 2 hours concomitant with elevation of MUC5AC protein production and mRNA expression in the different experiment groups (all P<0.05). Compared with single shear stress-stimulated group, MUC5AC in supernatant was increased obviously, and the distribution of F-actin in cytomembrane was also increased in the pEGFP-N1-Cort group (both P<0.05), while there were no changes in the MUC5AC protein and mRNA levels in cytoplasm. Compared with the shear stress+pEGFP-N1-Cort group, the MUC5AC protein in the culture supernatant was decreased, and the polymerization of F-actin at cell membranes were also attenuated in the shear stress+pEGFP-N1-Cort-Y421A group and the shear stress + pEGFP-N1-Cort-Y470A group (both P<0.05), while there was no significant effect in the shear stress + pEGFP-N1-Cort-Y486A group (P>0.05).
 Conclusion: Cortactin is involved in shear stress-mediated MUC5AC secretion in human airway epithelial cells, and the phosphorylated site of Tyr421 and Tyr470 may play an important role in it.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Muco Limite: Humans Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Muco Limite: Humans Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article