Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/21569
Title: Mast cells promote scar remodeling and functional recovery after spinal cord injury via mouse mast cell protease 6
Authors: VANGANSEWINKEL, Tim 
GEURTS, Nathalie 
Quanten, Kirsten
NELISSEN, Sofie 
LEMMENS, Stefanie 
GEBOES, Lies 
DOOLEY, Dearbhaile 
VIDAL VERA, Pia 
Pejler, Gunnar
HENDRIX, Sven 
Issue Date: 2016
Publisher: FEDERATION AMER SOC EXP BIOL
Source: FASEB JOURNAL, 30 (5), p. 2040-2057
Abstract: An important barrier for axon regeneration and recovery after traumatic spinal cord injury (SCI) is attributed to the scar that is formed at the lesion site. Here, we investigated the effect of mouse mast cell protease (mMCP) 6, a mast cell (MC)-specific tryptase, on scarring and functional recovery after a spinal cord hemisection injury. Functional recovery was significantly impaired in both MC-deficient and mMCP6-knockout (mMCP6(-/-)) mice after SCI compared with wild-type control mice. This decrease in locomotor performance was associated with an increased lesion size and excessive scarring at the injury site. Axon growth-inhibitory chondroitin sulfate proteoglycans and the extracellular matrix components fibronectin, laminin, and collagen IV were significantly up-regulated in MC-deficient and mMCP6(-/-) mice, with an increase in scar volume between 23 and 32%. A degradation assay revealed that mMCP6 directly cleaves fibronectin and collagen IV in vitro. In addition, gene expression levels of the scar components fibronectin, aggrecan, and collagen IV were increased up to 6.8-fold in mMCP6(-/-) mice in the subacute phase after injury. These data indicate that endogenous mMCP6 has scar-suppressing properties after SCI via indirect cleavage of axon growth-inhibitory scar components and alteration of the gene expression profile of these factors.-Vangansewinkel, T., Geurts, N., Quanten, K., Nelissen, S., Lemmens, S., Geboes, L., Dooley, D., Vidal, P. M., Pejler, G., Hendrix, S. Mast cells promote scar remodeling and functional recovery after spinal cord injury via mouse mast cell protease 6. www.fasebj.org
Notes: [Vangansewinkel, Tim; Geurts, Nathalie; Quanten, Kirsten; Nelissen, Sofie; Lemmens, Stefanie; Geboes, Lies; Dooley, Dearbhaile; Vidal, Pia M.; Hendrix, Sven] Hasselt Univ, Biomed Res Inst, Dept Morphol, Diepenbeek, Belgium. [Pejler, Gunnar] Swedish Univ Agr Sci, Dept Anat Physiol & Biochem, Uppsala, Sweden. [Pejler, Gunnar] Uppsala Univ, Dept Med Biochem & Microbiol, Uppsala, Sweden. [Vidal, Pia M.] Univ Hlth Network, Div Genet & Dev, Krembil Neurosci Ctr, Toronto, ON, Canada.
Keywords: CNS trauma; mMCP6; ECM remodeling; gene expression; improved outcome;CNS trauma; mMCP6; ECM remodeling; gene expression; improved outcome
Document URI: http://hdl.handle.net/1942/21569
ISSN: 0892-6638
e-ISSN: 1530-6860
DOI: 10.1096/fj.201500114R
ISI #: 000374879400030
Rights: © FASEB
Category: A1
Type: Journal Contribution
Validations: ecoom 2017
Appears in Collections:PhD theses
Research publications

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