Moyer P D, Kaufman A H, Zhang Z, Kao C W, Spaulding A G, Kao W W
Department of Ophthalmology, University of Cincinnati College of Medicine, OH 45267-0527, USA.
Differentiation. 1996 Mar;60(1):31-8. doi: 10.1046/j.1432-0436.1996.6010031.x.
Limbal stem cell deficiency contributes to recurrent corneal epithelial defects. We examined whether the conjunctival epithelium can transdifferentiate to corneal epithelium following surgically induced limbal stem cell deficiency. Mice were anesthetized by intraperitoneal injection of sodium pentobarbital. Partial or total epithelial removal was produced with a no. 69 Beaver blade under a dissecting microscope. The wounds were allowed to heal for 0-28 days, and the mice were examined every other day to evaluate re-epithelialization. Corneas were then subjected to histological, immunohistochemical studies and Western blot analysis with epitope-specific anti-keratin 12 antibodies. Partial epithelial defects re-epithelialized within 2 days and were normal in appearance and expressed cornea-specific keratin 12. In eyes with limbal deficiency, re-epithelialization progressed more slowly and was characterized by opacification; epithelial closure usually occurred by the 7th day. This epithelium differed from normal corneal epithelium in basic morphology, cell shape, and the presence of goblet cells at 2 weeks after injury. The epithelium at the center of injured corneas with total defect at 4 weeks had cornealike morphology and was devoid of goblet cells. These epithelial cells derived from conjunctiva did not express the cornea-specific keratin 12 as determined by immunohistochemistry, Western blot analysis and in situ hybridization. As evidenced by differences in morphology and the expression of cornea-specific keratin 12, conjunctival transdifferentiation does not occur in conjunctical overgrowth after the removal of limbal epithelium.
角膜缘干细胞缺乏会导致复发性角膜上皮缺损。我们研究了在手术诱导角膜缘干细胞缺乏后,结膜上皮是否能转分化为角膜上皮。通过腹腔注射戊巴比妥钠对小鼠进行麻醉。在解剖显微镜下用69号比弗刀片进行部分或全部上皮切除。让伤口愈合0至28天,每隔一天检查小鼠以评估再上皮化情况。然后对角膜进行组织学、免疫组织化学研究以及用表位特异性抗角蛋白12抗体进行蛋白质印迹分析。部分上皮缺损在2天内实现再上皮化,外观正常并表达角膜特异性角蛋白12。在角膜缘缺乏的眼中,再上皮化进展较慢且以混浊为特征;上皮闭合通常在第7天发生。在损伤后2周时,这种上皮在基本形态、细胞形状以及杯状细胞的存在方面与正常角膜上皮不同。在4周时完全缺损的损伤角膜中央的上皮具有类似角膜的形态且没有杯状细胞。通过免疫组织化学、蛋白质印迹分析和原位杂交确定,这些源自结膜的上皮细胞不表达角膜特异性角蛋白12。形态学差异以及角膜特异性角蛋白12的表达证明,在角膜缘上皮切除后结膜过度生长中不会发生结膜转分化。