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DIFFERENTIATION AND TRANSDIFFERENTIATION IN VITRO OF NEURAL RETINA FROM MUTANT CHICKENS WITH HYPERPLASIC LENS EPITHELIUM 1)
Author(s) -
KONDOH HISATO,
YASUDA KUNIO,
OKADA T. S.,
CLAYTON R. M.
Publication year - 1980
Publication title -
development, growth and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 66
eISSN - 1440-169X
pISSN - 0012-1592
DOI - 10.1111/j.1440-169x.1980.00875.x
Subject(s) - transdifferentiation , biology , microbiology and biotechnology , lens (geology) , in vitro , embryonic stem cell , cellular differentiation , embryo , cell culture , retina , cell type , cell , stem cell , genetics , neuroscience , gene , paleontology
Mutant chickens, Hy‐1 and Hy‐2, show abnormalities in growth and differentiation of the lens epithelium. In this study, neural retinal cells (NR cells) from 3.5‐day‐old embryos of these mutants were cultured, and the differentiation in vitro was compared with the cells of the normal strain. Hy‐1 cells in vitro were characterized by a delay in the first appearance of neuronal cells (N‐cells) and by excessive production of this cell type at later stages. By contrast, the Hy‐2 cells were indistinguishable from the normal cells in the early phase of culturing. In spite of the marked difference of Hy‐1 NR cells in neuronal differentiation up to about 7 days in culture, the transdifferentiation of lens and pigmented cells occurred to a similar extent and with the same time schedule as cultures of normal cells. A number of lentoid bodies were formed by about 10 days. The relative composition of the three major classes of crystallins in transdifferentiated lens cells was almost identical between normal and Hy‐1 strains. The results were discussed in comparison with the previous results of cell culture of NR of 8‐day embryonic mutant chickens, and it was concluded that the process of transdifferentiation in cell culture is different between NR from 3.5‐day‐old and 8‐day‐old embryos.