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体外免疫组织化学评估化学和机械刺激对人牙龈成纤维细胞中环磷酸腺苷(cAMP)和前列腺素E水平的影响。

Immunohistochemical assessment of the effect of chemical and mechanical stimuli on cAMP and prostaglandin E levels in human gingival fibroblasts in vitro.

作者信息

Ngan P W, Crock B, Varghese J, Lanese R, Shanfeld J, Davidovitch Z

机构信息

Department of Orthodontics, Ohio State University, College of Dentistry, Columbus 43210.

出版信息

Arch Oral Biol. 1988;33(3):163-74. doi: 10.1016/0003-9969(88)90041-6.

Abstract

These were evaluated by: (1) a combined immunohistochemical-microphotometric procedure (IH) and (2) conventional radiometric assays. Human gingival fibroblasts were in the sixth passage, grown and maintained in Dulbecco minimal essential medium (DMEM) supplemented with 10 per cent horse serum. For chemical and hormonal stimuli, cells (2 x 10(4] were seeded on tissue-culture chamber/slides, and incubated with graded doses of either parathyroid hormone (PTH) or prostaglandin E2 (PGE2) for assessment of their adenosine-3',5'-monophosphate (cAMP) levels, and with indomethacin or colchicine for their effect on PGE levels. For mechanical stimuli, cells (1 x 10(6] were seeded on culture dishes with a flexible plastic membrane and stretched for 5, 30, 60 or 120 min by placing the membrane over a convex surface and weighting the dish cover. After freeze drying, cells were stained by an immunoperoxidase technique for either cAMP or PGE, using monoclonal antibodies. The staining intensity of fibroblasts was determined at 600 nm wavelength. Per cent light absorbance of 15 cells in each slide was measured and the results tested by analysis of variance. The gingival fibroblasts responded to the drugs and hormones in a dose- and time-related fashion. Stretching significantly increased their synthesis of PGE with concomitant increase in cAMP. The IH results were compared with the radiometric assays to confirm the validity of this technique; both assays were valid for describing the quantitative responses of these cells to the stimuli. In particular, the IH method could localize those intracellular sites which demonstrated chances in relative cAMP and PGE concentrations in response to hormonal stimuli.

摘要

这些通过以下方法进行评估

(1)免疫组织化学 - 显微光度法联合检测(IH)和(2)传统放射测定法。人牙龈成纤维细胞处于第六代,在补充有10%马血清的杜尔贝科改良伊格尔培养基(DMEM)中培养和维持。对于化学和激素刺激,将细胞(2×10⁴)接种在组织培养室/载玻片上,并用不同剂量的甲状旁腺激素(PTH)或前列腺素E2(PGE2)孵育以评估其环磷酸腺苷(cAMP)水平,并用吲哚美辛或秋水仙碱评估其对PGE水平的影响。对于机械刺激,将细胞(1×10⁶)接种在带有柔性塑料膜的培养皿上,通过将膜置于凸面上并加重培养皿盖的重量来拉伸5、30、60或120分钟。冻干后,使用单克隆抗体通过免疫过氧化物酶技术对细胞进行cAMP或PGE染色。在600nm波长下测定成纤维细胞的染色强度。测量每张载玻片上15个细胞的吸光度百分比,并通过方差分析对结果进行检验。牙龈成纤维细胞对药物和激素的反应呈剂量和时间依赖性。拉伸显著增加了它们的PGE合成,并伴随cAMP增加。将IH结果与放射测定法进行比较以确认该技术的有效性;两种测定法都可有效描述这些细胞对刺激的定量反应。特别是,IH方法可以定位那些在激素刺激下细胞内相对cAMP和PGE浓度发生变化的部位。

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