Bosco L, Testa O, Venturini G, Willems D
Department of Animal and Human Biology, University La Sapienza, Rome, Italy.
Cell Mol Life Sci. 1997 Dec;53(11-12):921-8. doi: 10.1007/pl00013198.
The outer cornea of larval Xenopus laevis can reprogram cell differentiation when cultured in medium conditioned by X. laevis neural retina (XRCM) or by Rana esculenta neural retina (RRCM). Under these experimental conditions corneal cells showed the same series of cytological changes of fibre cell differentiation observed during ontogenesis and in vivo lens regeneration: enlargement of nuclei and nucleoli, increase of ribosomal population (cytoplasm-basophilia), cell elongation gradual loss of basophilic properties and acquisition of acidophilic properties for crystallin synthesis and accumulation. These events were completely dependent on XRCM or RRCM, suggesting that the neural retina secretes a factor(s) which initiates and sustains lens fibre transdifferentiation of the corneal epithelial cells. This culture system appears to be a suitable one for investigating the control of lens fibre transdifferentiation in vitro.
非洲爪蟾幼体的角膜外层在由非洲爪蟾神经视网膜(XRCM)或食用蛙神经视网膜(RRCM)条件培养基中培养时,能够重新编程细胞分化。在这些实验条件下,角膜细胞呈现出在个体发育和体内晶状体再生过程中观察到的纤维细胞分化的相同系列细胞学变化:细胞核和核仁增大、核糖体数量增加(细胞质嗜碱性)、细胞伸长、嗜碱性特性逐渐丧失以及获得用于晶状体蛋白合成和积累的嗜酸性特性。这些事件完全依赖于XRCM或RRCM,这表明神经视网膜分泌一种因子,该因子启动并维持角膜上皮细胞向晶状体纤维的转分化。这种培养系统似乎是体外研究晶状体纤维转分化控制的合适系统。