Murakami M, Tada K, Nakajima K, Kudo I
Department of Health Chemistry, School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.
J Immunol. 1997 Jul 1;159(1):439-46.
When rat serosal connective tissue mast cells (CTMC) were stimulated with nerve growth factor (NGF), the immediate prostaglandin D2 (PGD2) generation was followed by delayed PGD2 generation that occurred between 2 and 24 h, reaching levels as high as 50 ng and 260 ng/10(6) cells in the absence or presence of lysophosphatidylserine (lysoPS), respectively. This delayed PGD2 generation was accompanied by de novo induction of cyclooxygenase (COX)-2, with NGF and lysoPS acting as inducer and enhancer, respectively. COX-2 induction and the attendant delayed PGD2 generation in CTMC were modestly induced by c-kit ligand, but not by Fc epsilonRI cross-linking. This indicated that the stimulus specificity differed from that observed in the immediate phase, in which NGF, c-kit ligand, and Fc epsilonRI cross-linking, either in combination with each other or with lysoPS as a cofactor, elicited comparable levels of PGD2 generation within 10 min, reaching 10 to 20 ng/10(6) cells. Addition of type II secretory phospholipase A2 (sPLA2), a PLA2 isoform that is detected in microg/ml levels in inflammatory exudates, to NGF-stimulated CTMC significantly augmented delayed, but not immediate, PGD2 generation, and this augmentative effect was mediated in part by the enhancement of COX-2 expression by sPLA2. These results suggest that CTMC have the capacity to produce PGD2 over a prolonged period in the presence of tissue-derived cytokines and sPLA2 in a COX-2-dependent manner.
当用神经生长因子(NGF)刺激大鼠浆膜结缔组织肥大细胞(CTMC)时,前列腺素D2(PGD2)会先立即生成,随后在2至24小时之间出现延迟生成,在不存在或存在溶血磷脂酰丝氨酸(lysoPS)的情况下,分别达到高达50 ng和260 ng/10⁶细胞的水平。这种延迟的PGD2生成伴随着环氧化酶(COX)-2的从头诱导,NGF和lysoPS分别作为诱导剂和增强剂。c-kit配体可适度诱导CTMC中的COX-2诱导及随之而来的延迟PGD2生成,但FcεRI交联则无此作用。这表明刺激特异性与即刻阶段观察到的不同,在即刻阶段,NGF、c-kit配体和FcεRI交联,彼此组合或与lysoPS作为辅助因子,在10分钟内引发相当水平的PGD2生成,达到10至20 ng/10⁶细胞。向NGF刺激的CTMC中添加II型分泌型磷脂酶A2(sPLA2),一种在炎症渗出物中以微克/毫升水平检测到的PLA2同工型,可显著增强延迟而非即刻的PGD2生成,且这种增强作用部分是由sPLA2增强COX-2表达介导的。这些结果表明,在存在组织衍生细胞因子和sPLA2的情况下,CTMC有能力以COX-2依赖的方式在较长时间内产生PGD2。