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Title: Activity and localization of the Secretory Pathway Ca2+-ATPase isoform 1 (SPCA1) in different areas of the mouse brain during postnatal development
Authors: Sepulveda, Maria Rosario ×
Marcos, Daniel
Berrocal, Maria
Raeymaekers, Luc
Mata, Ana M
Wuytack, Frank #
Issue Date: Aug-2008
Publisher: Academic Press
Series Title: Molecular and Cellular Neurosciences vol:38 issue:4 pages:461-473
Abstract: Ca2+ and Mn2+ play an important role in many events in the nervous system, ranging from neural morphogenesis to neurodegeneration. As part of the homeostatic control of these ions, the Secretory Pathway Ca2+-ATPase isoform 1 (SPCA 1) mediates the accumulation of Ca2+ or Mn2+ with high affinity into Golgi reservoirs. This SPCA 1 represents a relatively recently characterized P-type pump that is highly expressed in nervous tissue, but information on its involvement in neural maturation is currently lacking. In this study, we have analyzed the expression and distribution of the SPCA 1 pump in mouse brain during postnatal development. RT-PCR and Western blot assays showed that SPCA 1 is particularly highly expressed at nearly constant levels during this entire period of development in cortex, hippocampus, and cerebellum. In spite of the apparently unchanged expression levels, functional assays showed that SPCA-associated Ca2+-ATPase activity increased with the stage of development in these areas. Immunohistochemical studies pointed to SPCA 1 localization in Golgi stacks of the soma and the initial part of primary dendritic trunk in main cortical, hippocampal and cerebellar neurons from the earliest postnatal stages. This suggests a potential role in intracellular signaling and in Golgi secretory processes involved in dendritic growth and in functional maturation of the mouse nervous system. (C) 2008 Elsevier Inc. All rights reserved.
URI: 
ISSN: 1044-7431
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Cellular Transport Systems
× corresponding author
# (joint) last author

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