Literature DB >> 7623106

Developmental determinants at the mammalian optic chiasm.

R W Guillery1, C A Mason, J S Taylor.   

Abstract

The mammalian optic chiasm is widely and properly regarded as a region where axons from the temporal retina take an uncrossed course and separate from axons arising in the nasal retina that take a crossed course. However, this is but a rough approximation of the adult situation, and developmental studies must take account of several distinctive stages and axon rearrangements that characterize the region of the chiasm. At the early and late stages of development of nonprimate species the axons do not segregate in accordance with a strict naso-temporal rule at all, and their behavior at the chiasm is not relevant to the formation of the naso-temporal division. As the axons pass from the eye to the chiasm they tend to lose their retinotopic order, to gain a chronotopic order, and then, in the region of the chiasm, to regain some aspects of the retinotopic order before reaching their terminal sites. Molecular or cellular cues that allow the several distinct organizational steps to occur must be expected in the retina, on the axons themselves, and also along the pathway of the axons, prechiasmatically and at the chiasm. Some of these cues will be associated with local nerve cells, some with specialized glial elements and some with the retinofugal axons themselves. Several candidate molecules have been identified in the retina and along the path of the axons, but to date no clearly defined role in the specific events of the pathway determination have been identified. The sequence of developmental processes that characterizes the formation of the optic chiasm provides an interesting and useful challenge to experimentalists, because the advancing axons can now be observed in vitro and in the living brain. The pattern of growth changes as development proceeds, it shows distinctive properties in different species and in their genetic mutants, and it can be readily modified by simple experimental procedures. These all provide opportunities for investigating the function of proposed molecular cues that act in the development of the chiasm.

Entities:  

Mesh:

Year:  1995        PMID: 7623106      PMCID: PMC6577905     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  27 in total

1.  Genesis, neurotrophin responsiveness, and apoptosis of a pronounced direct connection between the two eyes of the chick embryo: a natural error or a meaningful developmental event?

Authors:  S Thanos
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

2.  Roles of the telencephalic cells and their chondroitin sulfate proteoglycans in delimiting an anterior border of the retinal pathway.

Authors:  H Ichijo; I Kawabata
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

Review 3.  Cellular strategies of axonal pathfinding.

Authors:  Jonathan Raper; Carol Mason
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-06-30       Impact factor: 10.005

Review 4.  Development of the retina and optic pathway.

Authors:  Benjamin E Reese
Journal:  Vision Res       Date:  2010-07-18       Impact factor: 1.886

Review 5.  Conversations with Ray Guillery on albinism: linking Siamese cat visual pathway connectivity to mouse retinal development.

Authors:  Carol Mason; Ray Guillery
Journal:  Eur J Neurosci       Date:  2019-04-23       Impact factor: 3.386

Review 6.  Transcriptional regulation of guidance at the midline and in motor circuits.

Authors:  Aref Arzan Zarin; Jamshid Asadzadeh; Juan-Pablo Labrador
Journal:  Cell Mol Life Sci       Date:  2013-08-06       Impact factor: 9.261

Review 7.  Axonal commissures in the central nervous system: how to cross the midline?

Authors:  Homaira Nawabi; Valérie Castellani
Journal:  Cell Mol Life Sci       Date:  2011-05-03       Impact factor: 9.261

8.  Growth cone form is behavior-specific and, consequently, position-specific along the retinal axon pathway.

Authors:  C A Mason; L C Wang
Journal:  J Neurosci       Date:  1997-02-01       Impact factor: 6.167

9.  Ephrin-B2 elicits differential growth cone collapse and axon retraction in retinal ganglion cells from distinct retinal regions.

Authors:  Timothy J Petros; J Barney Bryson; Carol Mason
Journal:  Dev Neurobiol       Date:  2010-09-15       Impact factor: 3.964

10.  Tyrosinase expression during neuroblast divisions affects later pathfinding by retinal ganglion cells.

Authors:  Carolyn A Cronin; Amy B Ryan; Edmund M Talley; Heidi Scrable
Journal:  J Neurosci       Date:  2003-12-17       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.