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Changes in expression of fibroblast growth factor receptors during development of the mouse retinofugal pathway
Author(s) -
Lin Ling,
Taylor Jeremy S.H.,
Chan SunOn
Publication year - 2002
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.10337
Subject(s) - biology , optic tract , fibroblast growth factor receptor , inner plexiform layer , axon , retina , optic chiasm , fibroblast growth factor , retinal , microbiology and biotechnology , outer plexiform layer , immunostaining , neuroscience , immunocytochemistry , axon guidance , retinal ganglion cell , optic nerve , receptor , immunohistochemistry , endocrinology , immunology , genetics , biochemistry
Abstract Retinal axons undergo several changes in organization as they pass through the region of the optic chiasm and optic tract. We used immunocytochemistry to examine the possible involvement of fibroblast growth factor receptors (FGFR) in these changes in retinal axon growth. In the retina, at all ages examined, prominent staining for FGFR was seen in the optic fiber layer and at the optic disk. At embryonic day 15 (E15), FGFR immunoreactivity was also detected in the ganglion cell layer, as defined by immunoreactivity for islet‐1. At later developmental stages (E16 to postnatal day 0), FGFR were found in the optic fiber layer and the inner plexiform layer. In the ventral diencephalon, immunostaining for FGFR was first detected at E13 in a group of cells posterior to the chiasm. These cells appeared to match the neurons that are immunopositive for the stage‐specific embryonic antigen‐1 (SSEA‐1). FGFR staining was also found on the retinal axons at E13. At E14–E16, when most axons are growing across the chiasm and the tract, a dynamic pattern of FGFR immunoreactivity was observed on the retinal axons. The staining was reduced when axons reached the midline but was increased when axons reached the threshold of the optic tract. These results suggest that axon growth and fiber patterning in distinct regions of the retinofugal pathway are in part controlled by a regulated expression of FGFR. Furthermore, the axons with elevated FGFR expression in the optic tract have a posterior border of rich FGFR expression in the lateral part of the diencephalon. This region overlaps with a lateral extension of the SSEA‐1‐positive cells, suggesting a possible relation of these cells to the elevated expression of FGFR. J. Comp. Neurol. 451:22–32, 2002. © 2002 Wiley‐Liss, Inc.