Literature DB >> 2190790

The spatiotemporal distribution of N-CAM in the retinotectal pathway of adult goldfish detected by the monoclonal antibody D3.

M Bastmeyer1, B Schlosshauer, C A Stuermer.   

Abstract

The spatiotemporal distribution of neural cell adhesion molecule (N-CAM) in the retinotectal system of adult goldfish was assessed by immunofluorescence using the monoclonal antibody (Mab) D3 against chick N-CAM. In immunoblots with extracts of cell surface membranes of fish brains, Mab D3 recognized a prominent band at 170K and a weak band at 130K (K = 10(3) Mr). N-CAM immunofluorescence on cells was restricted to the marginal growth zones of the retina and the tectum and, in normal fish, to the youngest axons from the new ganglion cells of the peripheral retinal margin. In fish with previously transected optic nerves (ONS), Mab D3 staining was found transiently on all axons from the site of the cut into the retinorecipient layers of the tectum, but disappeared from these axons 450 days after ONS. Growing retinal axons in vitro exhibited N-CAM immunofluorescence throughout their entire extent, including their growth cones. Glial cells cultured from regenerating optic nerves were, however, unlabeled. These data are consistent with the idea that N-CAM is involved in adhesive interactions of growing axons. The temporally regulated expression of N-CAM on the new retinal axons may contribute to the creation of the age-related organization of the axons in the retinotectal pathway of fish.

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Year:  1990        PMID: 2190790     DOI: 10.1242/dev.108.2.299

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  8 in total

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Authors:  Lan-Yi Chang; Anne-Marie Mir; Christine Thisse; Yann Guérardel; Philippe Delannoy; Bernard Thisse; Anne Harduin-Lepers
Journal:  Glycoconj J       Date:  2008-07-20       Impact factor: 2.916

2.  Distribution of NCAM-180 and polysialic acid in the developing tectum mesencephali of the frog Discoglossus pictus and the salamander Pleurodeles waltl.

Authors:  C G Becker; T Becker; G Roth
Journal:  Cell Tissue Res       Date:  1993-05       Impact factor: 5.249

3.  A purine-sensitive pathway regulates multiple genes involved in axon regeneration in goldfish retinal ganglion cells.

Authors:  B Petrausch; R Tabibiazar; T Roser; Y Jing; D Goldman; C A Stuermer; N Irwin; L I Benowitz
Journal:  J Neurosci       Date:  2000-11-01       Impact factor: 6.167

4.  Neurolin, the goldfish homolog of DM-GRASP, is involved in retinal axon pathfinding to the optic disk.

Authors:  H Ott; M Bastmeyer; C A Stuermer
Journal:  J Neurosci       Date:  1998-05-01       Impact factor: 6.167

5.  Readiness of zebrafish brain neurons to regenerate a spinal axon correlates with differential expression of specific cell recognition molecules.

Authors:  T Becker; R R Bernhardt; E Reinhard; M F Wullimann; E Tongiorgi; M Schachner
Journal:  J Neurosci       Date:  1998-08-01       Impact factor: 6.167

6.  Neurolin, a cell surface glycoprotein on growing retinal axons in the goldfish visual system, is reexpressed during retinal axonal regeneration.

Authors:  K A Paschke; F Lottspeich; C A Stuermer
Journal:  J Cell Biol       Date:  1992-05       Impact factor: 10.539

7.  Fish E587 glycoprotein, a member of the L1 family of cell adhesion molecules, participates in axonal fasciculation and the age-related order of ganglion cell axons in the goldfish retina.

Authors:  M Bastmeyer; H Ott; C A Leppert; C A Stuermer
Journal:  J Cell Biol       Date:  1995-08       Impact factor: 10.539

8.  Neurolin Ig domain 2 participates in retinal axon guidance and Ig domains 1 and 3 in fasciculation.

Authors:  C A Leppert; H Diekmann; C Paul; U Laessing; M Marx; M Bastmeyer; C A Stuermer
Journal:  J Cell Biol       Date:  1999-01-25       Impact factor: 10.539

  8 in total

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