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Conference Paper: Chondroitin sulfate proteoglycans in astrocyte-Schwann cell cocultures limit neurite extension and crossing of cellular boundaries
Title | Chondroitin sulfate proteoglycans in astrocyte-Schwann cell cocultures limit neurite extension and crossing of cellular boundaries |
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Authors | |
Issue Date | 2006 |
Publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/NSG |
Citation | The Hong Kong Society of Neurosciences 24th Annual Scientific Meeting, Hong Kong, 13-14 January 2005. In Neurosignals, 2006, v. 15 n. 3, p. 126 How to Cite? |
Abstract | Axon regeneration in the injured spinal cord was restricted at
the interface between Schwann cell graft and the host astrocytes.
Chondroitin sulfate proteoglycans (CSPG) are implicated in the
axon-restrictive property of the interface [1] . Astrocytes and
Schwann cells were cocultured to mimic the in vivo situation. In
the cocultures, we found that: (1) cocultures stained live with the
CS56 showed pericellular immunopositivity on Schwann cells;
(2) PGs recovered from conditioned medium were digested with
chondroitinase and the disaccharide products showed dominance
of Di4S over Di6S as assayed with fluorophore-assisted carbohydrate
electrophoresis (FACE); (3) RT-PCR for chondroitin 6-
sulfotransferase (C6ST) and chondroitin 4-sulfotransferase
(C4ST) mRNAs showed dominance of C4ST over C6ST; (4) FACE
analysis of the pericellular matrix recovered from the cocultures
indicated hyaluronan and non-sulfated chondroitin. Taken together,
this suggests that CSPGs enriched in 4-sulfated chondroitins
were secreted into the medium, but hyaluronan and non-sulfated
chondroitins were immobilized at the cell surface. Next, we
seeded cortical neurons (E18 rats) on the astrocyte-Schwann cell
coculture and studied the consequent neurite growth pattern. We
found that: (1) neurons extended neurites along Schwann cell
processes, contrasting the multidirectional growth on astrocytes;
(2) neurites growing on astrocytes hardly changed course to grow
on Schwann cells. Chondroitinase ABC treatment to remove pericellular
CS and hyaluronan components indicated neurite growth
that could cross from astrocytes to Schwann cells; (3) the average
neurite length along Schwann cells was longer in Chondroitinase
ABC treated group than in the non-treated group. The results
suggest that immobilized non-sulfated chondroitins and hyaluronan
contribute to limiting neurite extension and crossing from
astrocyte to Schwann cells when Schwann cells meet astrocytes.
Reference
1 Chau CH, Shum DK, Li H, et al: FASEB J 2004; 18: 194–196. |
Persistent Identifier | http://hdl.handle.net/10722/96417 |
ISSN | 2016 Impact Factor: 6.143 2023 SCImago Journal Rankings: 0.458 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Liu, H | en_HK |
dc.contributor.author | Shum, DKY | en_HK |
dc.date.accessioned | 2010-09-25T16:33:10Z | - |
dc.date.available | 2010-09-25T16:33:10Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | The Hong Kong Society of Neurosciences 24th Annual Scientific Meeting, Hong Kong, 13-14 January 2005. In Neurosignals, 2006, v. 15 n. 3, p. 126 | en_HK |
dc.identifier.issn | 1424-862X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/96417 | - |
dc.description.abstract | Axon regeneration in the injured spinal cord was restricted at the interface between Schwann cell graft and the host astrocytes. Chondroitin sulfate proteoglycans (CSPG) are implicated in the axon-restrictive property of the interface [1] . Astrocytes and Schwann cells were cocultured to mimic the in vivo situation. In the cocultures, we found that: (1) cocultures stained live with the CS56 showed pericellular immunopositivity on Schwann cells; (2) PGs recovered from conditioned medium were digested with chondroitinase and the disaccharide products showed dominance of Di4S over Di6S as assayed with fluorophore-assisted carbohydrate electrophoresis (FACE); (3) RT-PCR for chondroitin 6- sulfotransferase (C6ST) and chondroitin 4-sulfotransferase (C4ST) mRNAs showed dominance of C4ST over C6ST; (4) FACE analysis of the pericellular matrix recovered from the cocultures indicated hyaluronan and non-sulfated chondroitin. Taken together, this suggests that CSPGs enriched in 4-sulfated chondroitins were secreted into the medium, but hyaluronan and non-sulfated chondroitins were immobilized at the cell surface. Next, we seeded cortical neurons (E18 rats) on the astrocyte-Schwann cell coculture and studied the consequent neurite growth pattern. We found that: (1) neurons extended neurites along Schwann cell processes, contrasting the multidirectional growth on astrocytes; (2) neurites growing on astrocytes hardly changed course to grow on Schwann cells. Chondroitinase ABC treatment to remove pericellular CS and hyaluronan components indicated neurite growth that could cross from astrocytes to Schwann cells; (3) the average neurite length along Schwann cells was longer in Chondroitinase ABC treated group than in the non-treated group. The results suggest that immobilized non-sulfated chondroitins and hyaluronan contribute to limiting neurite extension and crossing from astrocyte to Schwann cells when Schwann cells meet astrocytes. Reference 1 Chau CH, Shum DK, Li H, et al: FASEB J 2004; 18: 194–196. | - |
dc.language | eng | en_HK |
dc.publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/NSG | en_HK |
dc.relation.ispartof | Neurosignals | en_HK |
dc.rights | Neurosignals. Copyright © S Karger AG. | en_HK |
dc.title | Chondroitin sulfate proteoglycans in astrocyte-Schwann cell cocultures limit neurite extension and crossing of cellular boundaries | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1424-862X&volume=15&spage=126&epage=126&date=2006&atitle=Chondroitin+sulfate+proteoglycans+in+astrocyte-Schwann+cell+cocultures+limit+neurite+extension+and+crossing+of+cellular+boundaries | en_HK |
dc.identifier.email | Shum, DKY: shumdkhk@hkucc.hku.hk | en_HK |
dc.identifier.authority | Shum, DKY=rp00321 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1159/000095356 | - |
dc.identifier.hkuros | 129729 | en_HK |
dc.identifier.volume | 15 | en_HK |
dc.identifier.spage | 126 | en_HK |
dc.identifier.epage | 126 | en_HK |
dc.identifier.issnl | 1424-862X | - |