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环氧化酶-2依赖性前列腺素D2的延迟生成由大鼠腹膜肥大细胞中的神经生长因子引发:细胞外II型分泌性磷脂酶A2对其的增强作用。

Cyclooxygenase-2-dependent delayed prostaglandin D2 generation is initiated by nerve growth factor in rat peritoneal mast cells: its augmentation by extracellular type II secretory phospholipase A2.

作者信息

Murakami M, Tada K, Nakajima K, Kudo I

机构信息

Department of Health Chemistry, School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.

出版信息

J Immunol. 1997 Jul 1;159(1):439-46.

PMID:9200484
Abstract

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.

摘要

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。

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