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LRRK2 regulation of immune-pathways and inflammatory disease
Mutations in the leucine-rich-repeat kinase 2 (LRRK2) gene are associated with familial and sporadic cases of Parkinson's disease but are also found in immune-related disorders such as inflammatory bowel disease, tuberculosis and leprosy. LRRK2 is highly expressed in immune cells and has been f...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925522/ https://www.ncbi.nlm.nih.gov/pubmed/31769472 http://dx.doi.org/10.1042/BST20180463 |
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author | Wallings, Rebecca L. Tansey, Malú G. |
author_facet | Wallings, Rebecca L. Tansey, Malú G. |
author_sort | Wallings, Rebecca L. |
collection | PubMed |
description | Mutations in the leucine-rich-repeat kinase 2 (LRRK2) gene are associated with familial and sporadic cases of Parkinson's disease but are also found in immune-related disorders such as inflammatory bowel disease, tuberculosis and leprosy. LRRK2 is highly expressed in immune cells and has been functionally linked to pathways pertinent to immune cell function, such as cytokine release, autophagy and phagocytosis. Here, we examine the current understanding of the role of LRRK2 kinase activity in pathway regulation in immune cells, drawing upon data from multiple diseases associated with LRRK2 to highlight the pleiotropic effects of LRRK2 in different cell types. We discuss the role of the bona fide LRRK2 substrate, Rab GTPases, in LRRK2 pathway regulation as well as downstream events in the autophagy and inflammatory pathways. |
format | Online Article Text |
id | pubmed-6925522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69255222020-01-02 LRRK2 regulation of immune-pathways and inflammatory disease Wallings, Rebecca L. Tansey, Malú G. Biochem Soc Trans Review Articles Mutations in the leucine-rich-repeat kinase 2 (LRRK2) gene are associated with familial and sporadic cases of Parkinson's disease but are also found in immune-related disorders such as inflammatory bowel disease, tuberculosis and leprosy. LRRK2 is highly expressed in immune cells and has been functionally linked to pathways pertinent to immune cell function, such as cytokine release, autophagy and phagocytosis. Here, we examine the current understanding of the role of LRRK2 kinase activity in pathway regulation in immune cells, drawing upon data from multiple diseases associated with LRRK2 to highlight the pleiotropic effects of LRRK2 in different cell types. We discuss the role of the bona fide LRRK2 substrate, Rab GTPases, in LRRK2 pathway regulation as well as downstream events in the autophagy and inflammatory pathways. Portland Press Ltd. 2019-12-20 2019-11-26 /pmc/articles/PMC6925522/ /pubmed/31769472 http://dx.doi.org/10.1042/BST20180463 Text en © 2019 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Review Articles Wallings, Rebecca L. Tansey, Malú G. LRRK2 regulation of immune-pathways and inflammatory disease |
title | LRRK2 regulation of immune-pathways and inflammatory disease |
title_full | LRRK2 regulation of immune-pathways and inflammatory disease |
title_fullStr | LRRK2 regulation of immune-pathways and inflammatory disease |
title_full_unstemmed | LRRK2 regulation of immune-pathways and inflammatory disease |
title_short | LRRK2 regulation of immune-pathways and inflammatory disease |
title_sort | lrrk2 regulation of immune-pathways and inflammatory disease |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925522/ https://www.ncbi.nlm.nih.gov/pubmed/31769472 http://dx.doi.org/10.1042/BST20180463 |
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