首页> 外文OA文献 >Rabbit ileal villus cell brush border Na+/H+ exchange is regulated by Ca2+/calmodulin-dependent protein kinase II, a brush border membrane protein.
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Rabbit ileal villus cell brush border Na+/H+ exchange is regulated by Ca2+/calmodulin-dependent protein kinase II, a brush border membrane protein.

机译:兔回肠绒毛细胞刷状边界Na + / H +交换受刷状边界膜蛋白Ca2 + /钙调蛋白依赖性蛋白激酶II调控。

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摘要

Ileal brush border membranes contain an endogenous Ca2+/calmodulin (CaM)-dependent protein kinase activity that modulates the activity of the apical membrane Na+/H+ exchanger. To further characterize this kinase, synapsin I, a substrate for Ca2+/CaM-dependent protein kinases, was added to preparations of ileal brush border membranes. In the presence of Ca2+/CaM, synapsin I was phosphorylated. Phosphopeptide mapping demonstrated that the addition of Ca2+/CaM to brush border membranes stimulated the phosphorylation of sites in synapsin I specific for Ca2+/CaM-dependent protein kinase II. Immunoblots containing brush border and microvillus membrane proteins were probed with an antibody that recognizes the 50-kDa subunit of rat brain Ca2+/CaM-dependent protein kinase II. This antibody labeled major and minor species of 50 and 53 kDa, respectively, with more labeling of the brush border than the microvillus membranes. Right-side-out ileal villus cell brush border vesicles were prepared containing CaM, ATP, and 350 nM free Ca2+. Na+/H+ exchange was inhibited by the presence of Ca2+/CaM/ATP within the vesicles. A 21-amino acid peptide inhibitor of CaM kinase II was enclosed within some vesicle preparations by freeze-thaw. The effect on Na+/H+ exchange of Ca2+/CaM/ATP was partially reversed by the inhibitor peptide. These studies demonstrate the presence of Ca2+/CaM-dependent protein kinase II in rabbit ileal villus cell brush border membranes. Based on the effect of a specific inhibitor peptide of Ca2+/CaM kinase II, it is concluded that this kinase inhibits brush border Na+/H+ exchange, which participates in the regulation of ileal Na+ absorption.
机译:回肠刷状缘膜含有内源性Ca2 + /钙调蛋白(CaM)依赖性蛋白激酶活性,该活性调节顶膜Na + / H +交换子的活性。为了进一步表征该激酶,向回肠刷缘膜的制备物中添加了突触蛋白I(一种Ca2 + / CaM依赖性蛋白激酶的底物)。在Ca2 + / CaM存在下,突触素I被磷酸化。磷酸肽图分析表明,向刷状缘膜上添加Ca2 + / CaM可以刺激突触蛋白I中对Ca2 + / CaM依赖性蛋白激酶II特异的位点的磷酸化。用识别大鼠脑Ca2 + / CaM依赖性蛋白激酶II的50 kDa亚基的抗体探测含有刷状边界和微绒毛膜蛋白的免疫印迹。该抗体分别标记了50kDa和53kDa的主要和次要种类,与微绒毛膜相比,刷状缘的标记更多。制备含有CaM,ATP和350 nM游离Ca2 +的右侧向外回肠绒毛细胞刷缘囊泡。囊泡中Ca2 + / CaM / ATP的存在抑制了Na + / H +的交换。 CaM激酶II的21个氨基酸的肽抑制剂通过冻融封闭在一些囊泡制剂中。抑制剂肽可部分逆转对Ca2 + / CaM / ATP的Na + / H +交换的影响。这些研究表明在兔回肠绒毛细胞刷状缘膜中存在Ca2 + / CaM依赖性蛋白激酶II。基于Ca2 + / CaM激酶II的特定抑制剂肽的作用,可以得出结论,该激酶抑制了刷状缘Na + / H +的交换,参与了回肠Na +吸收的调节。

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