Li Weiwei, Sun Xuguang, Wang Zhiqun, Li Ran, Li Li
Beijing Institute of Ophthalmology, Beijing Ophthalmology & Visual Sciences Key Lab, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Bejing, China.
Mol Vis. 2010 Dec 15;16:2739-44.
To evaluate in vitro the effect of nerve growth factor (NGF) on the differentiation of mouse corneal limbal progenitor cells into goblet cells and to observe the expression of mucin-5AC (MUC5AC) mRNA.
Mouse limbal epithelial cells were cultured in a 1:1 mixture of Dulbecco's modified Eagle's medium/Ham's nutrient mixture F12 in vitro, and 63-kDa protein (p63) in cultured cells was identified with immunofluorescence staining. Different groups of the cultured cells were exposed to NGF at different concentrations (0 ng/ml, 10 ng/ml, 100 ng/ml, and 250 ng/ml). MUC5AC gene expression (real-time PCR) and goblet cell differentiation (MUC5AC immunofluorescence staining) were analyzed at different time points (24 h, 72 h, and 5 d).
In primary culture, the limbal epithelial cells were compact, uniform, and cobblestone pavement in shape. Some limbal epithelial cells were positive for p63. The MUC5AC-positive cells were detected when the cells were treated with 100 ng/ml NGF at each time point and with 250 ng/ml NGF at 5 d. The expression of MUC5AC mRNA increased when using 100 ng/ml NGF. The MUC5AC-positive cells were not detected when 0 ng/ml and 10 ng/ml NGF were used at each time point.
The results of this study suggest that NGF might promote the differentiation of corneal limbal progenitor cells into conjunctival goblet cells and upregulate the expression of MUC5AC mRNA in primary culture. Further studies using an animal model in vivo are needed.
在体外评估神经生长因子(NGF)对小鼠角膜缘祖细胞分化为杯状细胞的影响,并观察黏蛋白-5AC(MUC5AC)mRNA的表达。
将小鼠角膜缘上皮细胞在体外以1:1的杜氏改良 Eagle 培养基/哈姆氏营养混合物 F12 中培养,并用免疫荧光染色鉴定培养细胞中的63-kDa蛋白(p63)。将不同组的培养细胞暴露于不同浓度(0 ng/ml、10 ng/ml、100 ng/ml和250 ng/ml)的NGF中。在不同时间点(24小时、72小时和5天)分析MUC5AC基因表达(实时PCR)和杯状细胞分化(MUC5AC免疫荧光染色)。
在原代培养中,角膜缘上皮细胞紧密、均匀,呈鹅卵石铺路状。一些角膜缘上皮细胞p63呈阳性。在每个时间点用100 ng/ml NGF处理细胞以及在5天时用250 ng/ml NGF处理细胞时,检测到MUC5AC阳性细胞。使用100 ng/ml NGF时,MUC5AC mRNA的表达增加。在每个时间点使用0 ng/ml和10 ng/ml NGF时,未检测到MUC5AC阳性细胞。
本研究结果表明,NGF可能促进角膜缘祖细胞在原代培养中分化为结膜杯状细胞,并上调MUC5AC mRNA的表达。需要使用体内动物模型进行进一步研究。