蚌埠医学院学报
蚌埠醫學院學報
방부의학원학보
Journal of Bengbu Medical College
2015年
11期
1485-1487
,共3页
高自清%周琦%岳晓丽%李娟%李宁
高自清%週琦%嶽曉麗%李娟%李寧
고자청%주기%악효려%리연%리저
视网膜色素%上皮细胞%转化生长因子β1%细胞增殖%增殖性玻璃体视网膜病变
視網膜色素%上皮細胞%轉化生長因子β1%細胞增殖%增殖性玻璃體視網膜病變
시망막색소%상피세포%전화생장인자β1%세포증식%증식성파리체시망막병변
retinal pigment%epithelium%transforming growth factor β1%proliferation%proliferative vitreoretinopathy
目的::用氚-标记胸腺嘧啶核苷(3 H-TdR )掺入法观察转化生长因子β1( TGF-β1)对人视网膜色素上皮细胞( retinal pigment epithelium cells,RPE)增殖的影响,探讨TGF-β1和RPE细胞在增殖性玻璃体视网膜病变发病机制中的作用。方法:RPE细胞体外培养,用不同浓度的TGF-β10.1、1.0、5.0、10.0和100.0μg/L对细胞进行处理,3 H-TdR掺入法测定细胞放射性强度。结果:TGF-β10.1、1.0、5.0、10.0μg/L 作用后 RPE 活细胞数增加,细胞3H-TdR 摄入量均较对照组显著增加,TGF-β1100.0μg/L对RPE作用相反,细胞3H-TdR摄入量明显低于对照组(P<0.01)。结论:TGF-β1对人RPE细胞增殖有双相调节性,其不同作用的发挥依赖TGF-β1的浓度,其中TGF-β1促RPE细胞增殖作用是诱导增殖性玻璃体视网膜病变发生的可能机制之一。
目的::用氚-標記胸腺嘧啶覈苷(3 H-TdR )摻入法觀察轉化生長因子β1( TGF-β1)對人視網膜色素上皮細胞( retinal pigment epithelium cells,RPE)增殖的影響,探討TGF-β1和RPE細胞在增殖性玻璃體視網膜病變髮病機製中的作用。方法:RPE細胞體外培養,用不同濃度的TGF-β10.1、1.0、5.0、10.0和100.0μg/L對細胞進行處理,3 H-TdR摻入法測定細胞放射性彊度。結果:TGF-β10.1、1.0、5.0、10.0μg/L 作用後 RPE 活細胞數增加,細胞3H-TdR 攝入量均較對照組顯著增加,TGF-β1100.0μg/L對RPE作用相反,細胞3H-TdR攝入量明顯低于對照組(P<0.01)。結論:TGF-β1對人RPE細胞增殖有雙相調節性,其不同作用的髮揮依賴TGF-β1的濃度,其中TGF-β1促RPE細胞增殖作用是誘導增殖性玻璃體視網膜病變髮生的可能機製之一。
목적::용천-표기흉선밀정핵감(3 H-TdR )참입법관찰전화생장인자β1( TGF-β1)대인시망막색소상피세포( retinal pigment epithelium cells,RPE)증식적영향,탐토TGF-β1화RPE세포재증식성파리체시망막병변발병궤제중적작용。방법:RPE세포체외배양,용불동농도적TGF-β10.1、1.0、5.0、10.0화100.0μg/L대세포진행처리,3 H-TdR참입법측정세포방사성강도。결과:TGF-β10.1、1.0、5.0、10.0μg/L 작용후 RPE 활세포수증가,세포3H-TdR 섭입량균교대조조현저증가,TGF-β1100.0μg/L대RPE작용상반,세포3H-TdR섭입량명현저우대조조(P<0.01)。결론:TGF-β1대인RPE세포증식유쌍상조절성,기불동작용적발휘의뢰TGF-β1적농도,기중TGF-β1촉RPE세포증식작용시유도증식성파리체시망막병변발생적가능궤제지일。
Objective:To investigate the effects of transforming growth factorβ1 ( TGF-β1 ) on the proliferation of human retinal pigment epithelium( RPE ) cells by 3 H- thymidine deoxyribose ( 3 H-TdR ) absorption, and explore the pathogenesis mechanism of vitreoretinopathy. Methods:Human retinal pigment epithelium cells were cultured in vitro,the cells were incubated with 0. 1,1. 0,5. 0, 10. 0 and 100. 0 μg/L of TGF-β1 . The radioactivity intensity of cells were determined by 3 H-TdR absorption. Results:The 0. 1,1. 0,5. 0 and 10. 0 μg/L of TGF-β1 could promote the proliferation of RPE cells to increase the number of living cells,the intaking 3 H-TdR value of cells was significantly higher than that in control group(P <0. 01 ). The effects of the 100. 0 μg/L of TGF-β1 on the proliferation of RPE cells was opposite,the intaking 3H-TdR value of cells was significantly lower than that in control group(P<0. 01). Conclusions:The effect of TGF-β1 on the proliferation of RPE cells is dual regulation, different concentrations of TGF-β1 may have different effects on RPE cells. The effect of TGF-β1 on promoting the proliferation of RPE cells maybe one of mechanisms of proliferative vitreoretinopathy.