Occleston N L, Daniels J T, Tarnuzzer R W, Sethi K K, Alexander R A, Bhattacharya S S, Schultz G S, Khaw P T
International Collaborative Wound Research Group, Institute of Ophthalmology and Moorfields Eye Hospital, London, United Kingdom.
Invest Ophthalmol Vis Sci. 1997 Sep;38(10):1998-2007.
To determine the long-term effects of single, 5-minute exposures to 5-fluorouracil (5FU) and mitomycin-C (MMC) on Tenon's capsule fibroblast migration, growth factor production, growth factor receptor expression, and extracellular matrix (ECM) production.
Monolayer cultures and the overlying growth medium of Tenon's capsule fibroblasts exposed to 5FU (0.25 to 25 mg/ml) or MMC (0.001 to 0.1 mg/ml) were harvested up to 48 days after treatment. The expression of growth factors and growth factor receptors, including transforming growth factor beta (TGFbeta), basic fibroblast growth factor (bFGF), and epidermal growth factor (EGF), and ECM molecules (collagen type I, collagen type III, and fibronectin) were quantitated at the mRNA and protein levels. The ability of fibroblasts exposed to 5FU and MMC to migrate to fetal calf serum was also investigated up to 48 days after treatment.
Control cultures were found to produce the growth factors TGFbeta and bFGF but not EGF. Exposure to 5FU or MMC resulted in an initial significant increase (P < 0.05) in the production of TGFbeta and bFGF, with levels then decreasing toward those of controls. Cells exposed to 5FU or MMC exhibited an initial significant decrease (P < 0.05) in the number of TGFbeta, bFGF, and EGF growth factor receptors, with subsequent recovery toward control levels by day 48 after treatment. Both 5FU and MMC caused a significant reduction (P < 0.05) in collagen type I and fibronectin production compared to controls throughout the 48-day culture period. The production of collagen type III was initially elevated (P < 0.05) compared to controls after exposure to 5FU or MMC, production then decreasing toward control levels over the remainder of the 48-day culture period. The migration of cells exposed to 5FU or MMC was significantly reduced (P < 0.05) compared to controls up to 48 days after treatment; these cells exhibited a partial recovery of migratory ability throughout this period.
Fibroblasts whose growth was arrested using single, short exposures to 5FU or MMC appear to be capable of performing several crucial aspects of wound healing, including the expression of growth factors and receptors and ECM molecules and the ability to migrate. These findings may help explain why in some patients treated with antiproliferatives, glaucoma filtration surgery fails because of scarring.
确定单次5分钟暴露于5-氟尿嘧啶(5FU)和丝裂霉素-C(MMC)对眼球筋膜囊成纤维细胞迁移、生长因子产生、生长因子受体表达及细胞外基质(ECM)产生的长期影响。
在处理后长达48天收集暴露于5FU(0.25至25mg/ml)或MMC(0.001至0.1mg/ml)的眼球筋膜囊成纤维细胞单层培养物及其上覆生长培养基。在mRNA和蛋白质水平定量分析生长因子和生长因子受体的表达,包括转化生长因子β(TGFβ)、碱性成纤维细胞生长因子(bFGF)和表皮生长因子(EGF),以及ECM分子(I型胶原、III型胶原和纤连蛋白)。还研究了暴露于5FU和MMC的成纤维细胞在处理后长达48天向胎牛血清迁移的能力。
发现对照培养物产生生长因子TGFβ和bFGF,但不产生EGF。暴露于5FU或MMC导致TGFβ和bFGF产生最初显著增加(P<0.05),随后水平下降至对照水平。暴露于5FU或MMC的细胞TGFβ、bFGF和EGF生长因子受体数量最初显著减少(P<0.05),处理后第48天恢复至对照水平。在整个48天培养期内,与对照相比。5FU和MMC均导致I型胶原和纤连蛋白产生显著减少(P<0.05)。暴露于5FU或MMC后,III型胶原产生最初比对照升高(P<0.05),在48天培养期的其余时间内产生量随后降至对照水平。与对照相比,暴露于5FU或MMC后细胞的迁移在处理后长达48天显著减少(P<0.05);在整个这段时间内这些细胞迁移能力部分恢复。
使用单次短期暴露于5FU或MMC使生长停滞的成纤维细胞似乎能够执行伤口愈合的几个关键方面,包括生长因子和受体以及ECM分子的表达和迁移能力。这些发现可能有助于解释为什么在一些接受抗增殖药物治疗的患者中,青光眼滤过手术因瘢痕形成而失败。