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Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat
BACKGROUND: In the CNS, the heterotrimeric G protein Gα(i2 )is a minor Gα subunit with restricted localization in the ventricular regions including the ependymal cilia. The localization of Gα(i2 )is conserved in cilia of different tissues, suggesting a particular role in ciliary function. Although s...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1855344/ https://www.ncbi.nlm.nih.gov/pubmed/17430589 http://dx.doi.org/10.1186/1471-2202-8-26 |
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author | Mönkkönen, Kati S Hakumäki, Juhana M Hirst, Robert A Miettinen, Riitta A O'Callaghan, Christopher Männistö, Pekka T Laitinen, Jarmo T |
author_facet | Mönkkönen, Kati S Hakumäki, Juhana M Hirst, Robert A Miettinen, Riitta A O'Callaghan, Christopher Männistö, Pekka T Laitinen, Jarmo T |
author_sort | Mönkkönen, Kati S |
collection | PubMed |
description | BACKGROUND: In the CNS, the heterotrimeric G protein Gα(i2 )is a minor Gα subunit with restricted localization in the ventricular regions including the ependymal cilia. The localization of Gα(i2 )is conserved in cilia of different tissues, suggesting a particular role in ciliary function. Although studies with Gα(i2)-knockout mice have provided information on the role of this Gα subunit in peripheral tissues, its role in the CNS is largely unknown. We used intracerebroventricular (icv) antisense administration to clarify the physiological role of Gα(i2 )in the ventricular system. RESULTS: High resolution MRI studies revealed that continuous icv-infusion of Gα(i2)-specific antisense oligonucleotide caused unilateral ventricular dilatation that was restricted to the antisense-receiving ventricle. Microscopic analysis demonstrated ependymal cell damage and loss of ependymal cilia. Attenuation of Gα(i2 )in ependymal cells was confirmed by immunohistochemistry. Ciliary beat frequency measurements on cultured ependymal cells indicated that antisense administration resulted in ciliary stasis. CONCLUSION: Our results establish that Gα(i2 )has an essential regulatory role in ciliary function and CSF homeostasis. |
format | Text |
id | pubmed-1855344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18553442007-04-25 Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat Mönkkönen, Kati S Hakumäki, Juhana M Hirst, Robert A Miettinen, Riitta A O'Callaghan, Christopher Männistö, Pekka T Laitinen, Jarmo T BMC Neurosci Research Article BACKGROUND: In the CNS, the heterotrimeric G protein Gα(i2 )is a minor Gα subunit with restricted localization in the ventricular regions including the ependymal cilia. The localization of Gα(i2 )is conserved in cilia of different tissues, suggesting a particular role in ciliary function. Although studies with Gα(i2)-knockout mice have provided information on the role of this Gα subunit in peripheral tissues, its role in the CNS is largely unknown. We used intracerebroventricular (icv) antisense administration to clarify the physiological role of Gα(i2 )in the ventricular system. RESULTS: High resolution MRI studies revealed that continuous icv-infusion of Gα(i2)-specific antisense oligonucleotide caused unilateral ventricular dilatation that was restricted to the antisense-receiving ventricle. Microscopic analysis demonstrated ependymal cell damage and loss of ependymal cilia. Attenuation of Gα(i2 )in ependymal cells was confirmed by immunohistochemistry. Ciliary beat frequency measurements on cultured ependymal cells indicated that antisense administration resulted in ciliary stasis. CONCLUSION: Our results establish that Gα(i2 )has an essential regulatory role in ciliary function and CSF homeostasis. BioMed Central 2007-04-12 /pmc/articles/PMC1855344/ /pubmed/17430589 http://dx.doi.org/10.1186/1471-2202-8-26 Text en Copyright © 2007 Mönkkönen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mönkkönen, Kati S Hakumäki, Juhana M Hirst, Robert A Miettinen, Riitta A O'Callaghan, Christopher Männistö, Pekka T Laitinen, Jarmo T Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat |
title | Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat |
title_full | Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat |
title_fullStr | Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat |
title_full_unstemmed | Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat |
title_short | Intracerebroventricular antisense knockdown of Gα(i2 )results in ciliary stasis and ventricular dilatation in the rat |
title_sort | intracerebroventricular antisense knockdown of gα(i2 )results in ciliary stasis and ventricular dilatation in the rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1855344/ https://www.ncbi.nlm.nih.gov/pubmed/17430589 http://dx.doi.org/10.1186/1471-2202-8-26 |
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