Gulbins E, Szabo I, Baltzer K, Lang F
Department of Physiology, University of Tübingen, Gmelinstrasse 5, 72076 Tübingen, Germany.
Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7661-6. doi: 10.1073/pnas.94.14.7661.
The n-type K+ channel (n-K+, Kv1.3) in lymphocytes has been recently implicated in the regulation of Fas-induced programmed cell death. Here, we demonstrate that ceramide, a lipid metabolite synthesized upon Fas receptor ligation, inhibits n-K+ channel activity and induces a tyrosine phosphorylation of the Kv1.3 protein in Jurkat T lymphocytes. Tyrosine phosphorylation of the n-K+ channel correlated with an activation of the Src-like tyrosine kinase p56lck upon cellular treatment with the ceramide analog C6-ceramide. Because genetic deficiency of p56lck or inhibition of Src-like tyrosine kinases by herbimycin A prevented ceramide-mediated n-K+ channel inhibition and tyrosine phosphorylation, we propose a ceramide-initiated activation of p56lck resulting in tyrosine phosphorylation and inhibition of the n-K+ channel protein.
淋巴细胞中的n型钾通道(n-K+,Kv1.3)最近被认为与Fas诱导的程序性细胞死亡的调节有关。在此,我们证明,神经酰胺这种在Fas受体连接后合成的脂质代谢产物,可抑制Jurkat T淋巴细胞中的n-K+通道活性,并诱导Kv1.3蛋白的酪氨酸磷酸化。在用神经酰胺类似物C6-神经酰胺处理细胞后,n-K+通道的酪氨酸磷酸化与Src样酪氨酸激酶p56lck的激活相关。由于p56lck基因缺陷或除草霉素A对Src样酪氨酸激酶的抑制可阻止神经酰胺介导的n-K+通道抑制和酪氨酸磷酸化,我们提出神经酰胺启动p56lck的激活,导致酪氨酸磷酸化并抑制n-K+通道蛋白。