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A critical role for STIM1 in filopodial calcium entry and axon guidance
BACKGROUND: Stromal interaction molecule 1 (STIM1), a Ca(2+) sensor in the endoplasmic reticulum, regulates store-operated Ca(2+) entry (SOCE) that is essential for Ca(2+) homeostasis in many types of cells. However, if and how STIM1 and SOCE function in nerve growth cones during axon guidance remai...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907062/ https://www.ncbi.nlm.nih.gov/pubmed/24289807 http://dx.doi.org/10.1186/1756-6606-6-51 |
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author | Shim, Sangwoo Zheng, James Q Ming, Guo-li |
author_facet | Shim, Sangwoo Zheng, James Q Ming, Guo-li |
author_sort | Shim, Sangwoo |
collection | PubMed |
description | BACKGROUND: Stromal interaction molecule 1 (STIM1), a Ca(2+) sensor in the endoplasmic reticulum, regulates store-operated Ca(2+) entry (SOCE) that is essential for Ca(2+) homeostasis in many types of cells. However, if and how STIM1 and SOCE function in nerve growth cones during axon guidance remains to be elucidated. RESULTS: We report that STIM1 and transient receptor potential channel 1 (TRPC1)-dependent SOCE operates in Xenopus spinal growth cones to regulate Ca(2+) signaling and guidance responses. We found that STIM1 works together with TRPC1 to mediate SOCE within growth cones and filopodia. In particular, STIM1/TRPC1-dependent SOCE was found to mediate oscillatory filopodial Ca(2+) transients in the growth cone. Disruption of STIM1 function abolished filopodial Ca(2+) transients and impaired Ca(2+)-dependent attractive responses of Xenopus growth cones to netrin-1. Finally, interference with STIM1 function was found to disrupt midline axon guidance of commissural interneurons in the developing Xenopus spinal cord in vivo. CONCLUSIONS: Our data demonstrate that STIM1/TRPC1-dependent SOCE plays an essential role in generating spatiotemporal Ca(2+) signals that mediate guidance responses of nerve growth cones. |
format | Online Article Text |
id | pubmed-3907062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39070622014-01-31 A critical role for STIM1 in filopodial calcium entry and axon guidance Shim, Sangwoo Zheng, James Q Ming, Guo-li Mol Brain Research BACKGROUND: Stromal interaction molecule 1 (STIM1), a Ca(2+) sensor in the endoplasmic reticulum, regulates store-operated Ca(2+) entry (SOCE) that is essential for Ca(2+) homeostasis in many types of cells. However, if and how STIM1 and SOCE function in nerve growth cones during axon guidance remains to be elucidated. RESULTS: We report that STIM1 and transient receptor potential channel 1 (TRPC1)-dependent SOCE operates in Xenopus spinal growth cones to regulate Ca(2+) signaling and guidance responses. We found that STIM1 works together with TRPC1 to mediate SOCE within growth cones and filopodia. In particular, STIM1/TRPC1-dependent SOCE was found to mediate oscillatory filopodial Ca(2+) transients in the growth cone. Disruption of STIM1 function abolished filopodial Ca(2+) transients and impaired Ca(2+)-dependent attractive responses of Xenopus growth cones to netrin-1. Finally, interference with STIM1 function was found to disrupt midline axon guidance of commissural interneurons in the developing Xenopus spinal cord in vivo. CONCLUSIONS: Our data demonstrate that STIM1/TRPC1-dependent SOCE plays an essential role in generating spatiotemporal Ca(2+) signals that mediate guidance responses of nerve growth cones. BioMed Central 2013-12-01 /pmc/articles/PMC3907062/ /pubmed/24289807 http://dx.doi.org/10.1186/1756-6606-6-51 Text en Copyright © 2013 Shim 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Shim, Sangwoo Zheng, James Q Ming, Guo-li A critical role for STIM1 in filopodial calcium entry and axon guidance |
title | A critical role for STIM1 in filopodial calcium entry and axon guidance |
title_full | A critical role for STIM1 in filopodial calcium entry and axon guidance |
title_fullStr | A critical role for STIM1 in filopodial calcium entry and axon guidance |
title_full_unstemmed | A critical role for STIM1 in filopodial calcium entry and axon guidance |
title_short | A critical role for STIM1 in filopodial calcium entry and axon guidance |
title_sort | critical role for stim1 in filopodial calcium entry and axon guidance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907062/ https://www.ncbi.nlm.nih.gov/pubmed/24289807 http://dx.doi.org/10.1186/1756-6606-6-51 |
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