White S R, Sigrist K S, Spaethe S M
Department of Medicine, University of Chicago, Illinois 60637.
Am J Physiol. 1993 Sep;265(3 Pt 1):L234-42. doi: 10.1152/ajplung.1993.265.3.L234.
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)
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)