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蛋白激酶C激活剂可诱导非洲爪蟾卵母细胞中表达的II型钠-磷酸盐共转运体的膜回收。

Protein kinase C activators induce membrane retrieval of type II Na+-phosphate cotransporters expressed in Xenopus oocytes.

作者信息

Forster I C, Traebert M, Jankowski M, Stange G, Biber J, Murer H

机构信息

Institute of Physiology, University of Zurich, Zurich, Switzerland.

出版信息

J Physiol. 1999 Jun 1;517 ( Pt 2)(Pt 2):327-40. doi: 10.1111/j.1469-7793.1999.0327t.x.

Abstract
  1. The rate of inorganic phosphate (Pi) reabsorption in the mammalian kidney is determined by the amount of type II sodium-coupled inorganic phosphate (Na+-Pi) cotransport protein present in the brush border membrane. Under physiological conditions, parathyroid hormone (PTH) leads to an inhibition of Na+-Pi cotransport activity, most probably mediated by the protein kinase A (PKA) and/or C (PKC) pathways. 2. In this study, PKC-induced inhibition of type II Na+-Pi cotransport activity was characterized in Xenopus laevis oocytes using electrophysiological and immunodetection techniques. Transport function was quantified in terms of Pi-activated current. 3. Oocytes expressing the type IIa rat renal, type IIb flounder renal or type IIb mouse intestinal Na+-Pi cotransporters lost > 50 % of Pi-activated transport function when exposed to the PKC activators DOG (1,2-dioctanoyl-sn-glycerol) or PMA (phorbol 12-myristate 13-acetate). DOG-induced inhibition was partially reduced with the PKC inhibitors staurosporine and bisindolylmaleimide I. Oocytes exposed to the inactive phorbol ester 4alpha-PDD (4alpha-phorbol 12,13-didecanoate) showed no significant loss of cotransporter function. 4. Oocytes expressing the rat renal Na+-SO42- cotransporter alone, or coexpressing this with the type IIa rat renal Na+-Pi cotransporter, showed no downregulation of SO42--activated cotransport activity by DOG. 5. Steady-state and presteady-state voltage-dependent kinetics of type II Na+-Pi cotransporter function were unaffected by DOG. 6. DOG induced a decrease in membrane capacitance which indicated a reduction in membrane area, thereby providing evidence for PKC-mediated endocytosis. 7. Immunocytochemical studies showed a redistribution of type II Na+-Pi cotransporters from the oolemma to the submembrane region after DOG treatment. Surface biotinylation confirmed a DOG-induced internalization of the transport protein. 8. These findings document a specific retrieval of exogenous type II Na+-Pi cotransporters induced by activation of a PKC pathway in the Xenopus oocyte.
摘要
  1. 哺乳动物肾脏中无机磷酸盐(Pi)的重吸收速率由刷状缘膜中存在的II型钠偶联无机磷酸盐(Na⁺-Pi)共转运蛋白的量决定。在生理条件下,甲状旁腺激素(PTH)会抑制Na⁺-Pi共转运活性,这很可能是由蛋白激酶A(PKA)和/或C(PKC)途径介导的。2. 在本研究中,利用电生理和免疫检测技术在非洲爪蟾卵母细胞中对PKC诱导的II型Na⁺-Pi共转运活性抑制进行了表征。转运功能根据Pi激活电流进行定量。3. 表达IIa型大鼠肾脏、IIb型比目鱼肾脏或IIb型小鼠肠道Na⁺-Pi共转运蛋白的卵母细胞,在暴露于PKC激活剂DOG(1,2-二辛酰基-sn-甘油)或PMA(佛波醇12-肉豆蔻酸酯13-乙酸酯)时,Pi激活的转运功能丧失超过50%。DOG诱导的抑制作用被PKC抑制剂星形孢菌素和双吲哚马来酰亚胺I部分降低。暴露于无活性佛波酯4α-PDD(4α-佛波醇12,13-二癸酸酯)的卵母细胞共转运蛋白功能无显著丧失。4. 单独表达大鼠肾脏Na⁺-SO₄²⁻共转运蛋白或与IIa型大鼠肾脏Na⁺-Pi共转运蛋白共表达的卵母细胞,DOG对SO₄²⁻激活的共转运活性无下调作用。5. II型Na⁺-Pi共转运蛋白功能的稳态和前稳态电压依赖性动力学不受DOG影响。6. DOG导致膜电容降低,这表明膜面积减小,从而为PKC介导的内吞作用提供了证据。7. 免疫细胞化学研究表明,DOG处理后,II型Na⁺-Pi共转运蛋白从卵母细胞膜重新分布到膜下区域。表面生物素化证实了DOG诱导的转运蛋白内化。8. 这些发现证明了非洲爪蟾卵母细胞中PKC途径激活诱导的外源性II型Na⁺-Pi共转运蛋白的特异性回收。

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本文引用的文献

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Stoichiometry and Na+ binding cooperativity of rat and flounder renal type II Na+-Pi cotransporters.
Am J Physiol. 1999 Apr;276(4):F644-9. doi: 10.1152/ajprenal.1999.276.4.F644.
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