Department of Biochemistry, Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Mol Neurobiol. 2010 Jun;41(2-3):356-66. doi: 10.1007/s12035-010-8115-7. Epub 2010 Apr 13.
Acute inflammation is important for tissue repair; however, chronic inflammation contributes to neurodegeneration in Alzheimer's disease (AD) and occurs when glial cells undergo prolonged activation. In the brain, stress or damage causes the release of nucleotides and activation of the G(q) protein-coupled P2Y(2) nucleotide receptor subtype (P2Y(2)R) leading to pro-inflammatory responses that can protect neurons from injury, including the stimulation and recruitment of glial cells. P2Y(2)R activation induces the phosphorylation of the epidermal growth factor receptor (EGFR), a response dependent upon the presence of a SH3 binding domain in the intracellular C terminus of the P2Y(2)R that promotes Src binding and transactivation of EGFR, a pathway that regulates the proliferation of cortical astrocytes. Other studies indicate that P2Y(2)R activation increases astrocyte migration. P2Y(2)R activation by UTP increases the expression in astrocytes of alpha(V)beta(3/5) integrins that bind directly to the P2Y(2)R via an Arg-Gly-Asp (RGD) motif in the first extracellular loop of the P2Y(2)R, an interaction required for G(o) and G(12) protein-dependent astrocyte migration. In rat primary cortical neurons (rPCNs) P2Y(2)R expression is increased by stimulation with interleukin-1beta (IL-1beta), a pro-inflammatory cytokine whose levels are elevated in AD, in part due to nucleotide-stimulated release from glial cells. Other results indicate that oligomeric beta-amyloid peptide (Abeta(1-42)), a contributor to AD, increases nucleotide release from astrocytes, which would serve to activate upregulated P2Y(2)Rs in neurons. Data with rPCNs suggest that P2Y(2)R upregulation by IL-1beta and subsequent activation by UTP are neuroprotective, since this increases the non-amyloidogenic cleavage of amyloid precursor protein. Furthermore, activation of IL-1beta-upregulated P2Y(2)Rs in rPCNs increases the phosphorylation of cofilin, a cytoskeletal protein that stabilizes neurite outgrowths. Thus, activation of pro-inflammatory P2Y(2)Rs in glial cells can promote neuroprotective responses, suggesting that P2Y(2)Rs represent a novel pharmacological target in neurodegenerative and other pro-inflammatory diseases.
急性炎症对组织修复很重要;然而,在阿尔茨海默病 (AD) 中,慢性炎症会导致神经退行性变,并且当神经胶质细胞发生长期激活时就会发生这种情况。在大脑中,应激或损伤会导致核苷酸的释放和 G(q) 蛋白偶联 P2Y(2)核苷酸受体亚型 (P2Y(2)R) 的激活,从而引发促炎反应,保护神经元免受损伤,包括刺激和招募神经胶质细胞。P2Y(2)R 的激活诱导表皮生长因子受体 (EGFR) 的磷酸化,这种反应依赖于 P2Y(2)R 细胞内 C 末端 SH3 结合域的存在,该结合域促进 Src 的结合和 EGFR 的转激活,该途径调节皮质星形胶质细胞的增殖。其他研究表明,P2Y(2)R 的激活会增加星形胶质细胞的迁移。UTP 对 P2Y(2)R 的激活会增加星形胶质细胞中 alpha(V)beta(3/5)整联蛋白的表达,该蛋白通过 P2Y(2)R 第一细胞外环中的 Arg-Gly-Asp (RGD) 基序直接与 P2Y(2)R 结合,这种相互作用是 G(o) 和 G(12) 蛋白依赖性星形胶质细胞迁移所必需的。在大鼠原代皮质神经元 (rPCNs) 中,白细胞介素-1β (IL-1β) 刺激会增加 P2Y(2)R 的表达,IL-1β 是一种促炎细胞因子,其水平在 AD 中升高,部分原因是核苷酸刺激从神经胶质细胞中释放。其他结果表明,寡聚 beta-淀粉样肽 (Abeta(1-42)),一种 AD 的促成因素,会增加星形胶质细胞中的核苷酸释放,从而激活神经元中上调的 P2Y(2)R。rPCNs 的研究数据表明,IL-1β 上调 P2Y(2)R 并随后被 UTP 激活具有神经保护作用,因为这会增加淀粉样前体蛋白的非淀粉样生成裂解。此外,rPCNs 中 IL-1β 上调的 P2Y(2)R 的激活会增加细胞骨架蛋白丝切蛋白的磷酸化,该蛋白稳定神经突生长。因此,激活神经胶质细胞中的促炎 P2Y(2)R 可以促进神经保护反应,这表明 P2Y(2)R 是神经退行性变和其他促炎疾病的新的药理学靶点。