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Effect of wound healing and tissue transplantation on the navigation of axons in organ‐cultured embryonic chick eyes
Author(s) -
Halfter Willi
Publication year - 1993
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.903270309
Subject(s) - retina , biology , transplantation , anatomy , neuroepithelial cell , wound healing , embryonic stem cell , optic cup (embryology) , inner limiting membrane , pathology , microbiology and biotechnology , neuroscience , surgery , medicine , eye development , immunology , phenotype , biochemistry , gene
Wound closure and repair of embryonic neuroepithelium were studied in organ‐cultured embryonic retinae. Eyes from 3 to 4‐day‐old embryos were cultured after removing pieces of retinal tissue. During the subsequent 24 hours of incubation, the 150 to 200 μm wide holes in the retina closed completely. Histological studies showed that the wound closure was not accomplished by cell migration or cell proliferation, but by an approximation of the wound edges mediated by extracellular matrix fibrils of the vitreous body. The wound contraction facilitated the integration of transplants into the retinal neuroepithelium with a perfect alignment of the implants with the host at the vitreal surface. Within 24 hours, a continuous inner limiting membrane between transplant and host retina was established. The effect of wound healing and tissue transplantation on the navigation of optic axons in the retina was investigated. The wound contraction in the retina caused the optic axons near the lesion site to grow to the wound center, where the axons traversed the retina and formed a neuroma at the ventricular side, resembling the organization of axons at the optic disc. In the transplantation paradigm, axons from the host retina migrated into the transplant and vice versa. However, due to the wound contraction around the transplant, most axons grew into the interface between the transplant and host tissue. 1993 Wiley‐Liss, Inc.