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Type IV collagen reduces mucin 5AC secretion in three-dimensional cultured human primary airway epithelial cells

机译:IV型胶原蛋白可减少三维培养的人原代气道上皮细胞中粘蛋白5AC的分泌

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摘要

Mucin 5AC (MUC5AC) hypersecretion induces airway narrowing in patients with asthma, which leads to breathing problems. We investigated the regulation of MUC5AC secretion by extracellular matrix (ECM) proteins in human primary airway epithelial cells from patients with asthma. The addition of type IV collagen to three-dimensional cultured human primary airway epithelial cells, which mimics the airway surface, reduced MUC5AC secretion in the medium, while the addition of laminin increased MUC5AC secretion. Furthermore, the addition of fibronectin did not affect MUC5AC secretion. In particular, the repeated addition of a low concentration of type IV collagen demonstrated a cumulative effect on the reduction in MUC5AC secretion. Human primary cells incubated with type IV collagen showed downregulated extracellular signal-regulated kinase (ERK) activity, which induced MUC5AC hypersecretion but did not affect Akt activity. These results suggest that the addition of type IV collagen to the apical surface of primary cells downregulates MUC5AC secretion and has a cumulative effect on MUC5AC secretion which might be effected via the ERK signaling pathway.
机译:Mucin 5AC(MUC5AC)过度分泌会导致哮喘患者的气道狭窄,从而导致呼吸问题。我们研究了哮喘患者人原发气道上皮细胞中细胞外基质(ECM)蛋白对MUC5AC分泌的调节作用。向三维培养的人类气道上皮细胞(模仿气道表面)中添加IV型胶原蛋白可减少培养基中MUC5AC的分泌,而层粘连蛋白的添加可增加MUC5AC的分泌。此外,纤连蛋白的添加不影响MUC5AC的分泌。特别地,反复添加低浓度的IV型胶原蛋白显示出对减少MUC5AC分泌的累积作用。与IV型胶原蛋白孵育的人原代细胞显示出下调的细胞外信号调节激酶(ERK)活性,该活性诱导MUC5AC过度分泌,但不影响Akt活性。这些结果表明,将IV型胶原蛋白添加到原代细胞的顶表面会下调MUC5AC的分泌,并对MUC5AC的分泌产生累积影响,这可能是通过ERK信号通路实现的。

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