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MICALs in control of the cytoskeleton, exocytosis, and cell death
MICALs form an evolutionary conserved family of multidomain signal transduction proteins characterized by a flavoprotein monooxygenase domain. MICALs are being implicated in the regulation of an increasing number of molecular and cellular processes including cytoskeletal dynamics and intracellular t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SP Birkhäuser Verlag Basel
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221843/ https://www.ncbi.nlm.nih.gov/pubmed/21822644 http://dx.doi.org/10.1007/s00018-011-0787-2 |
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author | Zhou, Yeping Gunput, Rou-Afza F. Adolfs, Youri Pasterkamp, R. Jeroen |
author_facet | Zhou, Yeping Gunput, Rou-Afza F. Adolfs, Youri Pasterkamp, R. Jeroen |
author_sort | Zhou, Yeping |
collection | PubMed |
description | MICALs form an evolutionary conserved family of multidomain signal transduction proteins characterized by a flavoprotein monooxygenase domain. MICALs are being implicated in the regulation of an increasing number of molecular and cellular processes including cytoskeletal dynamics and intracellular trafficking. Intriguingly, some of these effects are dependent on the MICAL monooxygenase enzyme and redox signaling, while other functions rely on other parts of the MICAL protein. Recent breakthroughs in our understanding of MICAL signaling identify the ability of MICALs to bind and directly modify the actin cytoskeleton, link MICALs to the docking and fusion of exocytotic vesicles, and uncover MICALs as anti-apoptotic proteins. These discoveries could lead to therapeutic advances in neural regeneration, cancer, and other diseases. |
format | Online Article Text |
id | pubmed-3221843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | SP Birkhäuser Verlag Basel |
record_format | MEDLINE/PubMed |
spelling | pubmed-32218432011-12-27 MICALs in control of the cytoskeleton, exocytosis, and cell death Zhou, Yeping Gunput, Rou-Afza F. Adolfs, Youri Pasterkamp, R. Jeroen Cell Mol Life Sci Review MICALs form an evolutionary conserved family of multidomain signal transduction proteins characterized by a flavoprotein monooxygenase domain. MICALs are being implicated in the regulation of an increasing number of molecular and cellular processes including cytoskeletal dynamics and intracellular trafficking. Intriguingly, some of these effects are dependent on the MICAL monooxygenase enzyme and redox signaling, while other functions rely on other parts of the MICAL protein. Recent breakthroughs in our understanding of MICAL signaling identify the ability of MICALs to bind and directly modify the actin cytoskeleton, link MICALs to the docking and fusion of exocytotic vesicles, and uncover MICALs as anti-apoptotic proteins. These discoveries could lead to therapeutic advances in neural regeneration, cancer, and other diseases. SP Birkhäuser Verlag Basel 2011-08-06 2011 /pmc/articles/PMC3221843/ /pubmed/21822644 http://dx.doi.org/10.1007/s00018-011-0787-2 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Review Zhou, Yeping Gunput, Rou-Afza F. Adolfs, Youri Pasterkamp, R. Jeroen MICALs in control of the cytoskeleton, exocytosis, and cell death |
title | MICALs in control of the cytoskeleton, exocytosis, and cell death |
title_full | MICALs in control of the cytoskeleton, exocytosis, and cell death |
title_fullStr | MICALs in control of the cytoskeleton, exocytosis, and cell death |
title_full_unstemmed | MICALs in control of the cytoskeleton, exocytosis, and cell death |
title_short | MICALs in control of the cytoskeleton, exocytosis, and cell death |
title_sort | micals in control of the cytoskeleton, exocytosis, and cell death |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221843/ https://www.ncbi.nlm.nih.gov/pubmed/21822644 http://dx.doi.org/10.1007/s00018-011-0787-2 |
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