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嗜酸性粒细胞主要碱性蛋白引起的豚鼠气管上皮细胞前列腺素分泌

Prostaglandin secretion by guinea pig tracheal epithelial cells caused by eosinophil major basic protein.

作者信息

White S R, Sigrist K S, Spaethe S M

机构信息

Department of Medicine, University of Chicago, Illinois 60637.

出版信息

Am J Physiol. 1993 Sep;265(3 Pt 1):L234-42. doi: 10.1152/ajplung.1993.265.3.L234.

Abstract

We examined the effect of eosinophil major basic protein (MBP) on prostaglandin (PG) secretion from guinea pig tracheal epithelial (GPTE) cells. Primary cultures of GPTE cells were incubated with 10(-6) M MBP for up to 6 h and then stimulated with 10(-6) M bradykinin (BK). PGE2, 6-ketoprostaglandin F1 alpha (PGF1 alpha), PGF2 alpha, and thromboxane B2 (TxB2) concentrations in media were determined by enzyme-linked immunoabsorbent assay (EIA). Incubation with MBP for 6 h caused secretion of both PGE2 (17,614 +/- 4,416 vs. 1,426 +/- 555 pg/10(6) cells at baseline, P < 0.001, n = 7) and PGF2 alpha (20,303 +/- 5,724 vs. 3,790 +/- 1.075 pg/10(6) cells at baseline, P < 0.002, n = 7). Secretion of PGE2 and PGF2 alpha stimulated by MBP required at least 2 h. Incubation with MBP for 6 h also augmented the subsequent response to BK: PGE2 secretion was 29,215 +/- 6,853 vs. 3,445 +/- 1,041 pg/10(6) cells for BK alone (P < 0.0001), and PGF2 alpha secretion was 25,407 +/- 6,237 vs. 5,213 +/- 1,535 pg/10(6) cells for BK alone (P < 0.0001). MBP did not change 6-keto-PGF1 alpha and TxB2 secretion. Incubation of GPTE cells from seven animals with polylysine, a protein with mass and ion charge similar to MBP, for 2 h, both caused secretion of PGE2 (8,579 +/- 3,244 vs. 788 +/- 419 pg/10(6) cells at baseline, P < 0.01) and augmented the response to BK (12,732 +/- 4,788 vs. 1,653 +/- 680 pg/10(6) cells after BK alone, P < 0.005).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了嗜酸性粒细胞主要碱性蛋白(MBP)对豚鼠气管上皮(GPTE)细胞前列腺素(PG)分泌的影响。将GPTE细胞原代培养物与10⁻⁶ M MBP孵育长达6小时,然后用10⁻⁶ M缓激肽(BK)刺激。通过酶联免疫吸附测定(EIA)测定培养基中前列腺素E2(PGE2)、6-酮前列腺素F1α(PGF1α)、前列腺素F2α(PGF2α)和血栓素B2(TxB2)的浓度。与MBP孵育6小时导致PGE2(基线时为1,426±555 pg/10⁶细胞,孵育后为17,614±4,416 pg/10⁶细胞,P<0.001,n = 7)和PGF2α(基线时为3,790±1,075 pg/10⁶细胞,孵育后为20,303±5,724 pg/10⁶细胞,P<0.002,n = 7)分泌。MBP刺激的PGE2和PGF2α分泌至少需要2小时。与MBP孵育6小时也增强了随后对BK的反应:单独使用BK时PGE2分泌为3,445±1,041 pg/10⁶细胞,与MBP孵育后为29,215±6,853 pg/10⁶细胞(P<0.0001),单独使用BK时PGF2α分泌为5,213±1,535 pg/10⁶细胞,与MBP孵育后为25,407±6,237 pg/10⁶细胞(P<0.0001)。MBP未改变6-酮-PGF1α和TxB2的分泌。用与MBP质量和离子电荷相似的蛋白质聚赖氨酸孵育来自7只动物的GPTE细胞2小时,既导致PGE2分泌(基线时为788±419 pg/10⁶细胞,孵育后为8,579±3,244 pg/10⁶细胞,P<0.01),也增强了对BK的反应(单独使用BK后为1,653±680 pg/10⁶细胞,孵育后为12,732±4,788 pg/10⁶细胞,P<0.005)。(摘要截断于250字)

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