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Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane
Phosphatidylinositol(4,5) bisphosphate (PI(4,5)P(2)) has become a major focus in biochemistry, cell biology and physiology owing to its diverse functions at the plasma membrane. As a result, the functions of PI(4,5)P(2) can be explored in two separate and distinct roles – as a substrate for phosphol...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517351/ https://www.ncbi.nlm.nih.gov/pubmed/32844214 http://dx.doi.org/10.1042/EBC20200041 |
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author | Katan, Matilda Cockcroft, Shamshad |
author_facet | Katan, Matilda Cockcroft, Shamshad |
author_sort | Katan, Matilda |
collection | PubMed |
description | Phosphatidylinositol(4,5) bisphosphate (PI(4,5)P(2)) has become a major focus in biochemistry, cell biology and physiology owing to its diverse functions at the plasma membrane. As a result, the functions of PI(4,5)P(2) can be explored in two separate and distinct roles – as a substrate for phospholipase C (PLC) and phosphoinositide 3-kinase (PI3K) and as a primary messenger, each having unique properties. Thus PI(4,5)P(2) makes contributions in both signal transduction and cellular processes including actin cytoskeleton dynamics, membrane dynamics and ion channel regulation. Signalling through plasma membrane G-protein coupled receptors (GPCRs), receptor tyrosine kinases (RTKs) and immune receptors all use PI(4,5)P(2) as a substrate to make second messengers. Activation of PI3K generates PI(3,4,5)P(3) (phosphatidylinositol(3,4,5)trisphosphate), a lipid that recruits a plethora of proteins with pleckstrin homology (PH) domains to the plasma membrane to regulate multiple aspects of cellular function. In contrast, PLC activation results in the hydrolysis of PI(4,5)P(2) to generate the second messengers, diacylglycerol (DAG), an activator of protein kinase C and inositol(1,4,5)trisphosphate (IP(3)/I(1,4,5)P(3)) which facilitates an increase in intracellular Ca(2+). Decreases in PI(4,5)P(2) by PLC also impact on functions that are dependent on the intact lipid and therefore endocytosis, actin dynamics and ion channel regulation are subject to control. Spatial organisation of PI(4,5)P(2) in nanodomains at the membrane allows for these multiple processes to occur concurrently. |
format | Online Article Text |
id | pubmed-7517351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75173512020-10-02 Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane Katan, Matilda Cockcroft, Shamshad Essays Biochem Signaling Phosphatidylinositol(4,5) bisphosphate (PI(4,5)P(2)) has become a major focus in biochemistry, cell biology and physiology owing to its diverse functions at the plasma membrane. As a result, the functions of PI(4,5)P(2) can be explored in two separate and distinct roles – as a substrate for phospholipase C (PLC) and phosphoinositide 3-kinase (PI3K) and as a primary messenger, each having unique properties. Thus PI(4,5)P(2) makes contributions in both signal transduction and cellular processes including actin cytoskeleton dynamics, membrane dynamics and ion channel regulation. Signalling through plasma membrane G-protein coupled receptors (GPCRs), receptor tyrosine kinases (RTKs) and immune receptors all use PI(4,5)P(2) as a substrate to make second messengers. Activation of PI3K generates PI(3,4,5)P(3) (phosphatidylinositol(3,4,5)trisphosphate), a lipid that recruits a plethora of proteins with pleckstrin homology (PH) domains to the plasma membrane to regulate multiple aspects of cellular function. In contrast, PLC activation results in the hydrolysis of PI(4,5)P(2) to generate the second messengers, diacylglycerol (DAG), an activator of protein kinase C and inositol(1,4,5)trisphosphate (IP(3)/I(1,4,5)P(3)) which facilitates an increase in intracellular Ca(2+). Decreases in PI(4,5)P(2) by PLC also impact on functions that are dependent on the intact lipid and therefore endocytosis, actin dynamics and ion channel regulation are subject to control. Spatial organisation of PI(4,5)P(2) in nanodomains at the membrane allows for these multiple processes to occur concurrently. Portland Press Ltd. 2020-09 2020-08-26 /pmc/articles/PMC7517351/ /pubmed/32844214 http://dx.doi.org/10.1042/EBC20200041 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/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). Open access for this article was enabled by the participation of University College London in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC. |
spellingShingle | Signaling Katan, Matilda Cockcroft, Shamshad Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane |
title | Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane |
title_full | Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane |
title_fullStr | Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane |
title_full_unstemmed | Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane |
title_short | Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane |
title_sort | phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane |
topic | Signaling |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517351/ https://www.ncbi.nlm.nih.gov/pubmed/32844214 http://dx.doi.org/10.1042/EBC20200041 |
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