Besshoh Shintaro, Bawa Damanpreet, Teves Lucy, Wallace M Christopher, Gurd James W
Centre for the Neurobiology of Stress, University of Toronto at Scarborough, Toronto, Canada.
J Neurochem. 2005 Apr;93(1):186-94. doi: 10.1111/j.1471-4159.2004.03009.x.
Ischemia results in increased phosphorylation of NMDA receptors. To investigate the possible role of lipid rafts in this increase, lipid rafts and post-synaptic densities (PSDs) were isolated by the extraction of rat brain synaptosomes with Triton X-100 followed by sucrose density gradient centrifugation. Lipid rafts accounted for the majority of PSD-95, whereas SAP102 was predominantly located in PSDs. Between 50 and 60% of NMDA receptors were associated with lipid rafts. Greater than 85-90% of Src and Fyn were present in lipid rafts, whereas Pyk2 was mainly associated with PSDs. Lipid rafts and PSDs were isolated from animals subjected to 15 min of global ischemia followed by 6 h of recovery. Ischemia did not affect the yield, density, flotillin-1 or cholesterol content of lipid rafts. Following ischemia, the phosphorylation of NR1 by protein kinase C and tyrosine phosphorylation of NR2A and NR2B was increased in both lipid rafts and PSDs, with a greater increase in tyrosine phosphorylation occurring in the raft fraction. Following ischemia, NR1, NR2A and NR2B levels were elevated in PSDs and reduced in lipid rafts. The findings are consistent with a model involving close interaction between lipid rafts and PSDs and a role for lipid rafts in ischemia-induced signaling pathways.
缺血会导致NMDA受体磷酸化增加。为了研究脂筏在这种增加中可能发挥的作用,通过用Triton X-100提取大鼠脑突触体,然后进行蔗糖密度梯度离心,分离出脂筏和突触后致密物(PSD)。脂筏占PSD-95的大部分,而SAP102主要位于PSD中。50%至60%的NMDA受体与脂筏相关。超过85%至90%的Src和Fyn存在于脂筏中,而Pyk2主要与PSD相关。从经历15分钟全脑缺血并恢复6小时的动物中分离出脂筏和PSD。缺血不影响脂筏的产量、密度、小窝蛋白-1或胆固醇含量。缺血后,脂筏和PSD中蛋白激酶C对NR1的磷酸化以及NR2A和NR2B的酪氨酸磷酸化均增加,脂筏部分酪氨酸磷酸化的增加更为明显。缺血后,PSD中NR1、NR2A和NR2B水平升高,脂筏中则降低。这些发现与脂筏和PSD之间密切相互作用以及脂筏在缺血诱导信号通路中发挥作用的模型一致。