Expression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured Microglia

The presence of microglia at sites of CNS injury can potentially shift the balance between neuronal survival and death; however, the mechanisms regulating their mobilization to these sites are still poorly understood. Here I report that microglia express podosomes, short-lived, punctate organelles w...

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Bibliographic Details
Main Author: Vincent, Catherine
Other Authors: Schlichter, Lyanne C.
Language:en_ca
Published: 2012
Subjects:
SK3
SK
Online Access:http://hdl.handle.net/1807/35155
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spelling ndltd-TORONTO-oai-tspace.library.utoronto.ca-1807-351552013-11-02T04:07:58ZExpression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured MicrogliaVincent, CatherineMicrogliapodosomesSK3SK0379The presence of microglia at sites of CNS injury can potentially shift the balance between neuronal survival and death; however, the mechanisms regulating their mobilization to these sites are still poorly understood. Here I report that microglia express podosomes, short-lived, punctate organelles which adhere to and degrade extracellular matrix (ECM). Podosomes and related invadopodia of cancer cells have recently been the focus of much interest for their roles in migration and invasion. Microglial podosomes degraded ECM, providing impetus for further study of their function in microglia. Further, I report the Ca2+-activated SK3 channel as a novel component of the podosome core. While SK3 and SK4 channels are reported to play redundant roles in activated microglia (Kaushal et al., 2007; Schlichter et al., 2010), immunostaining work suggests that they are differentially regulated during microglial activation. Together, these results suggest unique functions for these channel subtypes in microglia.Schlichter, Lyanne C.2012-032013-03-19T17:35:43ZWITHHELD_ONE_YEAR2013-03-19T17:35:43Z2013-03-19Thesishttp://hdl.handle.net/1807/35155en_ca
collection NDLTD
language en_ca
sources NDLTD
topic Microglia
podosomes
SK3
SK
0379
spellingShingle Microglia
podosomes
SK3
SK
0379
Vincent, Catherine
Expression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured Microglia
description The presence of microglia at sites of CNS injury can potentially shift the balance between neuronal survival and death; however, the mechanisms regulating their mobilization to these sites are still poorly understood. Here I report that microglia express podosomes, short-lived, punctate organelles which adhere to and degrade extracellular matrix (ECM). Podosomes and related invadopodia of cancer cells have recently been the focus of much interest for their roles in migration and invasion. Microglial podosomes degraded ECM, providing impetus for further study of their function in microglia. Further, I report the Ca2+-activated SK3 channel as a novel component of the podosome core. While SK3 and SK4 channels are reported to play redundant roles in activated microglia (Kaushal et al., 2007; Schlichter et al., 2010), immunostaining work suggests that they are differentially regulated during microglial activation. Together, these results suggest unique functions for these channel subtypes in microglia.
author2 Schlichter, Lyanne C.
author_facet Schlichter, Lyanne C.
Vincent, Catherine
author Vincent, Catherine
author_sort Vincent, Catherine
title Expression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured Microglia
title_short Expression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured Microglia
title_full Expression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured Microglia
title_fullStr Expression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured Microglia
title_full_unstemmed Expression of Podosomes and Small-conductance Ca2+-activated K+ Channels in Cultured Microglia
title_sort expression of podosomes and small-conductance ca2+-activated k+ channels in cultured microglia
publishDate 2012
url http://hdl.handle.net/1807/35155
work_keys_str_mv AT vincentcatherine expressionofpodosomesandsmallconductanceca2activatedkchannelsinculturedmicroglia
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