» Articles » PMID: 11425904

Intact Aggrecan and Fragments Generated by Both Aggrecanse and Metalloproteinase-like Activities Are Present in the Developing and Adult Rat Spinal Cord and Their Relative Abundance is Altered by Injury

Overview
Journal J Neurosci
Specialty Neurology
Date 2001 Jun 27
PMID 11425904
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Aggrecan is a large proteoglycan (PG) that has been grouped with different PG families on the basis of its physical characteristics. These families include the chondroitin sulfate PGs, which appear to inhibit the migration of cells and axons during development. Although aggrecan has been studied primarily in cartilage, in the present study, tissue samples from developing, mature, and injured-adult rat spinal cords were used to determine whether aggrecan is present in the mammalian spinal cord. By the use of Western blot analysis, tissues were probed with aggrecan-specific antibodies (ATEGQV, TYKHRL, and LEC-7) and aggrecan-specific neoepitope antibodies (NITEGE, FVDIPEN, and TFKEEE) to identify full-length aggrecan and several fragments. Unlike many other aggrecan gene family members, aggrecan species were similar in embryonic day 14, postnatal day 1, and adult spinal cords. Spinal cord injury caused significant decreases in aggrecan. Partial recovery in some aggrecan species was evident by 2 weeks after injury. The presence of specific aggrecan neoepitopes suggested that aggrecan is cleaved in the spinal cord by both a disintegrin and metalloproteinase thrombospondin (also known as aggrecanase) and metalloproteinase-like activities. Many aggrecan species found in the spinal cord were similar to species in cartilage. Additional antibodies were used to identify two other aggrecan gene family members, neurocan and brevican, in the adult spinal cord. These studies present novel information on the aggrecan core protein species and enzymes involved in aggrecan cleavage in vivo in the rat spinal cord throughout development and after injury. They also provide the basis for investigating the function of aggrecan in the spinal cord.

Citing Articles

Neonatal Zika virus infection causes transient perineuronal net degradation.

Engel K, Lee H, Tewari B, Lewkowicz A, Ireland D, Manangeeswaran M Front Cell Neurosci. 2023; 17:1187425.

PMID: 37496706 PMC: 10366369. DOI: 10.3389/fncel.2023.1187425.


The Role and Modulation of Spinal Perineuronal Nets in the Healthy and Injured Spinal Cord.

Sanchez-Ventura J, Lane M, Udina E Front Cell Neurosci. 2022; 16:893857.

PMID: 35669108 PMC: 9163449. DOI: 10.3389/fncel.2022.893857.


ADAMTS-5: A difficult teenager turning 20.

Santamaria S Int J Exp Pathol. 2020; 101(1-2):4-20.

PMID: 32219922 PMC: 7306899. DOI: 10.1111/iep.12344.


Spatiotemporal distribution of chondroitin sulfate proteoglycans after optic nerve injury in rodents.

Pearson C, Solano A, Tilve S, Mencio C, Martin K, Geller H Exp Eye Res. 2019; 190:107859.

PMID: 31705897 PMC: 7096184. DOI: 10.1016/j.exer.2019.107859.


Sensory deafferentation modulates and redistributes neurocan in the rat auditory brainstem.

Heusinger J, Hildebrandt H, Illing R Brain Behav. 2019; 9(8):e01353.

PMID: 31271523 PMC: 6710208. DOI: 10.1002/brb3.1353.


References
1.
Schwartz N, Pirok 3rd E, Mensch Jr J, Domowicz M . Domain organization, genomic structure, evolution, and regulation of expression of the aggrecan gene family. Prog Nucleic Acid Res Mol Biol. 1999; 62:177-225. DOI: 10.1016/s0079-6603(08)60508-5. View

2.
Steindler D, OBrien T, Laywell E, Harrington K, Faissner A, Schachner M . Boundaries during normal and abnormal brain development: in vivo and in vitro studies of glia and glycoconjugates. Exp Neurol. 1990; 109(1):35-56. DOI: 10.1016/s0014-4886(05)80007-x. View

3.
Lark M, Williams H, Hoernner L, Weidner J, Ayala J, Harper C . Quantification of a matrix metalloproteinase-generated aggrecan G1 fragment using monospecific anti-peptide serum. Biochem J. 1995; 307 ( Pt 1):245-52. PMC: 1136769. DOI: 10.1042/bj3070245. View

4.
Doege K, Sasaki M, Horigan E, Hassell J, Yamada Y . Complete primary structure of the rat cartilage proteoglycan core protein deduced from cDNA clones. J Biol Chem. 1987; 262(36):17757-67. View

5.
Risling M, Fried K, Linda H, Carlstedt T, Cullheim S . Regrowth of motor axons following spinal cord lesions: distribution of laminin and collagen in the CNS scar tissue. Brain Res Bull. 1993; 30(3-4):405-14. DOI: 10.1016/0361-9230(93)90272-d. View