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人血清可降低丝裂霉素-C对人眼球筋膜成纤维细胞的细胞毒性。

Human serum reduces mitomycin-C cytotoxicity in human tenon's fibroblasts.

作者信息

Crowston Jonathan G, Wang Xiao Y, Khaw Peng T, Zoellner Hans, Healey Paul R

机构信息

Center for Vision Research, Westmead Hospital and Westmead Millennium Research Institute, Sydney, NSW, Australia.

出版信息

Invest Ophthalmol Vis Sci. 2006 Mar;47(3):946-52. doi: 10.1167/iovs.05-1048.

Abstract

PURPOSE

To determine the effect of human serum factors on mitomycin-C (MMC) cytotoxicity in cultured human subconjunctival Tenon's capsule fibroblasts.

METHODS

Fibroblast monolayers were treated with 5-minute applications of mitomycin-C (0.4 mg/mL) and incubated in culture medium with or without additional human serum. Fibroblast apoptosis was quantified by direct cell counts based on nuclear morphology, flow cytometry with annexin-V/propidium iodide, and a lactate dehydrogenase release assay. The number of viable fibroblasts and fibroblast proliferation were measured with a colorimetric MTT assay and by bromodeoxyuridine (BrdU) labeling.

RESULTS

Mitomycin-C induced significant levels of fibroblast apoptosis. The addition of human serum resulted in a 40% reduction in MMC-induced fibroblast apoptosis (range, 31.3%-55.3%; P = 0.021) as determined by nuclear morphology and a 32.4% reduction measured by annexin-V/PI. There was a corresponding dose-dependent increase in the number of viable fibroblasts. Serum did not restore proliferation in MMC-treated fibroblasts.

CONCLUSIONS

Factors present in human serum reduce MMC cytotoxicity in cultured human Tenon's fibroblasts. Human serum increased the number of viable fibroblasts by inhibiting MMC-induced fibroblast apoptosis. Serum factors access aqueous humor after trabeculectomy and may therefore influence the clinical outcome of MMC treatment.

摘要

目的

确定人血清因子对培养的人结膜下Tenon囊成纤维细胞中丝裂霉素C(MMC)细胞毒性的影响。

方法

将成纤维细胞单层用丝裂霉素C(0.4mg/mL)处理5分钟,然后在含有或不含有额外人血清的培养基中孵育。通过基于核形态的直接细胞计数、用膜联蛋白-V/碘化丙啶进行的流式细胞术以及乳酸脱氢酶释放测定来定量成纤维细胞凋亡。用比色法MTT测定和溴脱氧尿苷(BrdU)标记来测量存活成纤维细胞的数量和成纤维细胞增殖。

结果

丝裂霉素C诱导了显著水平的成纤维细胞凋亡。通过核形态测定,添加人血清导致MMC诱导的成纤维细胞凋亡减少40%(范围为31.3%-55.3%;P = 0.021),通过膜联蛋白-V/PI测量减少32.4%。存活成纤维细胞的数量相应地呈剂量依赖性增加。血清未恢复MMC处理的成纤维细胞的增殖。

结论

人血清中存在的因子降低了培养的人Tenon成纤维细胞中MMC的细胞毒性。人血清通过抑制MMC诱导的成纤维细胞凋亡增加了存活成纤维细胞的数量。小梁切除术后血清因子进入房水,因此可能影响MMC治疗的临床结果。

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