## Abstract The present research aims at showing the role played by the lens in inhibiting lensβforming transformations of the outer cornea of __Xenopus laevis__ tadpoles. Two types of experiment were carried out: 1) lentectomy and insertion of a Millipore filter disk at the side of the lens, and 2
DNA synthesis during lens regeneration in larvalXenopus laevis
β Scribed by Waggoner, Phillip R. ;Reyer, Randall W.
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 443 KB
- Volume
- 192
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Larvae of Xenopus laevis at stages 50β53 were lentectomized and then injected with tritiated thymidine at various times after lentectomy. In Series I, the animals were injected 1, 2, 3, 4, 6, 8, 10, 12, 15, or 17 days after lens removal and fixed three hours after injection. Autoradiographs of serial cross sections through the eyes were prepared. Increased incorporation of thymidine in the cells of the regenerating lens was first observed two days (stage 2) after lentectomy. All of the cells of the lens vesicle incorporated H^3^βthymidine until stage 4 at which time the cells in the inner wall of the vesicle began to differentiate into lens fibers. Labelling then became restricted to the peripheral cells (prospective lens epithelium and prospective lens fibers). At stage 5 of regeneration, only cells of the lens epithelium incorporated H^3^βthymidine. In Series II, animals injected three or four days after lentectomy were fixed daily from one to seven days after injection. Many stage 3 and stage 4 regenerates were recovered with label throughout and stage 5 regenerates were found, seven days after injection, with label over the lens fibers as well as over the lens epithelium.
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## Abstract Three different types of experiments were carried out to investigate the role of the lens in lensβforming transformations of the outer cornea of __Xenopus laevis__ tadpoles (at stage 51, as defined by Nieuwkoop and Faber, '56): 1) simple lentectomy; 2) incision of outer and inner cornea
## Abstract The lensβforming capacity of the pericorneal epidermis of __Xenopus laevis__ larvae at stage 51 has been investigated. The results obtained show that, whether or not the lens is present, the pericorneal epidermis can form a lens when it is in direct contact with the vitreous chamber of
## Abstract After lentectomy through the pupillary hole, the outer cornea of larval __Xenopus laevis__ can undergo transdifferentiation to regenerate a new lens. This process is elicited by inductive factor(s) produced by the neural retina and accumulated into the vitreous chamber. During embryogen
Lumbar ganglia innervating regenerating and normal hindlimbs were removed from larval Xenopus laevis at stage 56-57 (according to Nieuwkoop and Faber, '56) and implanted between the outer and inner corneas of larvae of the same species at stage 50. The control experiments consisted of implanting fra
In larval X. laevis the capacity to regenerate a lens under the influence of inductive factors present in the vitreous chamber is restricted to the outer cornea and pericorneal epidermis (Lentogenic Area, LA). However, in early embryos, the whole ectoderm is capable of responding to inductive factor