Nam M J, Thore C, Busija D
Department of Physiology and Pharmacology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27157-1083, USA.
Prostaglandins. 1995 Jul;50(1):33-45. doi: 10.1016/0090-6980(95)00087-q.
We examined the effects of interleukin-1 alpha (IL-1 alpha) and involvement of protein kinases on prostaglandin production in cultured ovine astroglia. Ovine astroglia were exposed to media alone, or 10 ng/mL IL-1 alpha and prostaglandin F2 alpha (PGF2 alpha) levels were analyzed using enzyme immunoassay. Application of IL-1 alpha augmented the production of PGF2 alpha at 4 h. Coapplication of H-7 (10-1000 microM) and staurosporine (0.1-10 microM), inhibitors of protein kinase C (PKC), blocked IL-1 alpha-induced PGF2 alpha production. IL-1 alpha increased cyclooxygenase (COX) activity while coapplication of staurosporine prevented an increase, implying that COX activity was dependent upon PKC activation. In contrast, forskolin, sodium nitroprusside, and cyclic nucleotide analogs alone did not affect prostaglandin production significantly, excluding the involvement of cAMP/cGMP-dependent protein kinases. Coapplication of quinacrine (10 microM) and bromophenacyl bromide (100 microM), inhibitors of phospholipase A2 (PLA2), prevented the IL-1 alpha-induced increases in PGF2 alpha production. Lastly, IL-1 alpha increased labeled arachidonic acid (AA) release whereas coaddition of quinacrine (10 microM) attenuated increased AA release. Therefore, we propose that IL-1 alpha enhances prostaglandin production by ovine astroglia via steps involving activation of PKC and increased activity of COX and PLA2.
我们研究了白细胞介素-1α(IL-1α)的作用以及蛋白激酶的参与对培养的绵羊星形胶质细胞中前列腺素产生的影响。将绵羊星形胶质细胞单独暴露于培养基中,或者暴露于10 ng/mL的IL-1α,然后使用酶免疫测定法分析前列腺素F2α(PGF2α)的水平。在4小时时,应用IL-1α可增加PGF2α的产生。蛋白激酶C(PKC)抑制剂H-7(10 - 1000 microM)和星形孢菌素(0.1 - 10 microM)共同应用可阻断IL-1α诱导的PGF2α产生。IL-1α增加了环氧化酶(COX)的活性,而星形孢菌素共同应用可阻止其增加,这意味着COX活性依赖于PKC的激活。相比之下,单独使用福司可林、硝普钠和环核苷酸类似物对前列腺素的产生没有显著影响,排除了cAMP/cGMP依赖性蛋白激酶的参与。磷脂酶A2(PLA2)抑制剂奎纳克林(10 microM)和溴苯甲酰溴(100 microM)共同应用可阻止IL-1α诱导的PGF2α产生增加。最后,IL-1α增加了标记的花生四烯酸(AA)释放,而奎纳克林(10 microM)共同添加可减弱AA释放的增加。因此,我们提出IL-1α通过涉及PKC激活以及COX和PLA2活性增加的步骤来增强绵羊星形胶质细胞中前列腺素的产生。