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PMID: 7680631 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

Developmental biology ·Vol. 156 ·No. 1 ·1993-03-00 ·Pages 34-48

Pindzola RR, Doller C, Silver J

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.

MeSH Terms
Aging/physiology Animals Cell Adhesion Molecules, Neuronal/analysis Chondroitin Sulfate Proteoglycans/analysis Embryonic and Fetal Development Extracellular Matrix/ultrastructure Extracellular Matrix Proteins/analysis,metabolism Female Gestational Age Glial Fibrillary Acidic Protein/analysis Nerve Crush Pregnancy Rats Rats, Sprague-Dawley Reference Values Sciatic Nerve/embryology,growth & development,physiology Spinal Cord/embryology,growth & development,physiology Spinal Nerve Roots/embryology,growth & development,physiology Tenascin Vimentin/analysis
Chemicals
Cell Adhesion Molecules, Neuronal Chondroitin Sulfate Proteoglycans Extracellular Matrix Proteins Glial Fibrillary Acidic Protein Tenascin Vimentin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pindzola R R
Department of Neurosciences, Case Western Reserve University, Cleveland, Ohio 44106-4975.
Doller C
Silver J
Article Info
Journal
Developmental biology
Abbr.
Dev Biol
ISSN
0012-1606
Published
1993-03-00
Pages
34-48
Language
English
Region
United States
NLM ID
0372762
Subset
IM
Grants
NINDS NIH HHS · NS-255713 · United States
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