Literature DB >> 7680631

Putative inhibitory extracellular matrix molecules at the dorsal root entry zone of the spinal cord during development and after root and sciatic nerve lesions.

R R Pindzola1, C Doller, J Silver.   

Abstract

The dorsal root entry zone (DREZ) of the spinal cord is the interface between the central and peripheral nervous systems and is the pathway through which sensory afferents enter the central nervous system during development. However, in the rat, the DREZ becomes a boundary to regenerating sensory axons after Postnatal Days 2-3. The cellular and molecular mechanisms that cause regenerative failure at the DREZ after the critical period for regeneration are unknown. Recent studies demonstrate that two extracellular matrix molecules, Cytotactin/tenascin (CT) and chondroitin 6-sulfate-containing proteoglycans (C-6S-PG) are present in normal boundary regions of the brain and spinal cord during development. In the present study we sought to visualize the expression of these two putative inhibitory molecules in the DREZ of normally developing and adult animals, and also in animals after injury. CT and C-6S-PG spread laterally from the midline to the DREZ by Postnatal Day 3, correlating exactly with the end of the critical period. The staining intensity for these two molecules increases further in the DREZ after root lesions, but not sciatic lesions, at ages when axons cannot regenerate into the spinal cord. Following root lesion CT and C-6S-PG were mostly present in association with reactive glia at the DREZ and in white matter, rather than with reactive glia in grey matter of the dorsal horn, suggesting that astroglia are heterogeneous in their response to root lesion. The coexpression of CT and C-6S-PG may create a molecular barrier which might channel or deflect axons at the DREZ during CNS development and inhibit their growth during regeneration.

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Year:  1993        PMID: 7680631     DOI: 10.1006/dbio.1993.1057

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  48 in total

1.  White matter of the CNS supports or inhibits neurite outgrowth in vitro depending on geometry.

Authors:  D B Pettigrew; K A Crutcher
Journal:  J Neurosci       Date:  1999-10-01       Impact factor: 6.167

2.  Two-tiered inhibition of axon regeneration at the dorsal root entry zone.

Authors:  M S Ramer; I Duraisingam; J V Priestley; S B McMahon
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

3.  Neurocan is upregulated in injured brain and in cytokine-treated astrocytes.

Authors:  R A Asher; D A Morgenstern; P S Fidler; K H Adcock; A Oohira; J E Braistead; J M Levine; R U Margolis; J H Rogers; J W Fawcett
Journal:  J Neurosci       Date:  2000-04-01       Impact factor: 6.167

4.  DSD-1-proteoglycan is the mouse homolog of phosphacan and displays opposing effects on neurite outgrowth dependent on neuronal lineage.

Authors:  J Garwood; O Schnädelbach; A Clement; K Schütte; A Bach; A Faissner
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

5.  Identification of a neurite outgrowth-promoting motif within the alternatively spliced region of human tenascin-C.

Authors:  S Meiners; M S Nur-e-Kamal; M L Mercado
Journal:  J Neurosci       Date:  2001-09-15       Impact factor: 6.167

6.  The critical role of basement membrane-independent laminin gamma 1 chain during axon regeneration in the CNS.

Authors:  Barbara Grimpe; Sucai Dong; Catherine Doller; Katherine Temple; Alfred T Malouf; Jerry Silver
Journal:  J Neurosci       Date:  2002-04-15       Impact factor: 6.167

Review 7.  The transitional zone and CNS regeneration.

Authors:  J P Fraher
Journal:  J Anat       Date:  1999-02       Impact factor: 2.610

8.  Chronic enhancement of the intrinsic growth capacity of sensory neurons combined with the degradation of inhibitory proteoglycans allows functional regeneration of sensory axons through the dorsal root entry zone in the mammalian spinal cord.

Authors:  Michael P Steinmetz; Kevin P Horn; Veronica J Tom; Jared H Miller; Sarah A Busch; Dileep Nair; Daniel J Silver; Jerry Silver
Journal:  J Neurosci       Date:  2005-08-31       Impact factor: 6.167

9.  Functional regeneration of chronically injured sensory afferents into adult spinal cord after neurotrophin gene therapy.

Authors:  M I Romero; N Rangappa; M G Garry; G M Smith
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

10.  Evidence for a role of the chemorepellent semaphorin III and its receptor neuropilin-1 in the regeneration of primary olfactory axons.

Authors:  R J Pasterkamp; F De Winter; A J Holtmaat; J Verhaagen
Journal:  J Neurosci       Date:  1998-12-01       Impact factor: 6.167

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