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唾液黏蛋白对颊黏膜钙通道活性的调节。

Regulation of buccal mucosal calcium channel activity by salivary mucins.

作者信息

Slomiany B L, Fekete Z, Murty V L, Grabska M, Piotrowski J, Yotsumoto F, Czajkowski A, Slomiany A

机构信息

Research Center, New Jersey Dental School, University of Medicine and Dentistry of New Jersey, Newark 07103-2400.

出版信息

Int J Biochem. 1993 Sep;25(9):1281-9. doi: 10.1016/0020-711x(93)90080-x.

Abstract
  1. The effect salivary mucins on the activity of calcium channel isolated from buccal mucosal cell membranes was investigated. The uptake of 45Ca2+ while only moderately (15%) affected by the intact low and high molecular weight mucin forms, was significantly inhibited, by the acidic low and high molecular weight salivary mucins which evoked 64 and 60% inhibition, respectively. 2. The inhibitory effect of salivary mucins was associated with the sialic acid and sulfate ester groups of the carbohydrate chains, as the removal of either group caused partial loss in the glycoproteins inhibition, and the complete loss in the inhibitory effect occurred following desialylation and desulfation. 3. The channel in the presence of epidermal growth factor (EGF) and ATP responded by an increase in tyrosine phosphorylation of 55 and 170 kDa proteins, and the phosphorylated channels showed a 46% increase in 45Ca2+ uptake. The phosphorylation and the calcium uptake were susceptible to inhibition by a specific tyrosine kinase inhibitor, genistein. 4. The binding of EGF to calcium channel receptor protein was inhibited by the low and high molecular weight acidic mucins, causing 41.2 and 36.1% reduction, respectively. This reduction in binding was dependent upon the presence of sulfate ester and sialic acid groups, as evidenced by the loss of the glycoproteins' inhibitory capacity following removal of these groups. 5. The results for the first time demonstrate that salivary mucins actively participate in the modulation of the EGF-controlled buccal mucosal calcium channel activity expression, a process of importance to the preservation of oral tissue integrity.
摘要
  1. 研究了唾液粘蛋白对从颊粘膜细胞膜分离的钙通道活性的影响。完整的低分子量和高分子量粘蛋白形式对45Ca2+的摄取仅有适度影响(15%),而酸性低分子量和高分子量唾液粘蛋白则显著抑制45Ca2+的摄取,分别引起64%和60%的抑制。2. 唾液粘蛋白的抑制作用与糖链的唾液酸和硫酸酯基团有关,因为去除任何一个基团都会导致糖蛋白抑制作用部分丧失,而在去唾液酸化和去硫酸化后抑制作用完全丧失。3. 在表皮生长因子(EGF)和ATP存在的情况下,通道的反应是55 kDa和170 kDa蛋白的酪氨酸磷酸化增加,磷酸化的通道45Ca2+摄取增加46%。磷酸化和钙摄取易受特异性酪氨酸激酶抑制剂染料木黄酮的抑制。4. 低分子量和高分子量酸性粘蛋白抑制EGF与钙通道受体蛋白的结合,分别导致结合减少41.2%和36.1%。这种结合减少取决于硫酸酯和唾液酸基团的存在,去除这些基团后糖蛋白抑制能力丧失证明了这一点。5. 结果首次表明,唾液粘蛋白积极参与EGF控制的颊粘膜钙通道活性表达的调节,这一过程对维持口腔组织完整性很重要。

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