Does PtdIns(4,5)P 2 concentrate so it can multi-task?
Abstract
Ptdns(4,5)P2 is a minor structural lipid of the plasma membrane (PM), but a master regulator of PM function. Serving either as a substrate for the generation of second messengers, or more commonly as a ligand triggering protein recruitment or activation, it regulates most aspects of PM function. Understanding how this relatively simple biological macromolecule can regulate such a vast array of different functions in parallel, is the key to understanding the biology of the PM as a whole, in both health and disease. In this review, potential mechanisms are discussed that might explain how a lipid can separately regulate so many protein complexes. The focus is on the spatial distribution of the lipid molecules, their metabolism and their interactions. Open questions that still need to be resolved are highlighted, as are potential experimental approaches that might shed light on the mechanisms at play. Moreover, the broader question is raised as to whether PtdIns(4,5)P2 should be thought of as a bona fide signalling molecule or more of a simple lipid cofactor or perhaps both, depending on the context of the particular function in question.
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There is strong evidence for PI(4,5)P2 segregation, but many caveats remain due to technical limitations.
“Although there is strong evidence to support segregation of PI(4,5)P2, as discussed above, there remains many caveats due to technical limitations [132,133].”
From Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane (2020) · cites this paper as [132]
Local enrichment of PI(4,5)P2 can occur by preferential trapping in lipid rafts, binding proteins such as MARCKS, syntaxin-1 and K-Ras, or localised recruitment of PIP5K.
“Local enrichment of PI(4,5)P2 can occur by multiple mechanisms [131,132]. There can be preferential trapping of PI(4,5)P2 in lipid rafts, binding proteins such as MARCKS (myristoylated alanine-rich C-kinase substrate), syntaxin-1 and K-Ras that sequester PI(4,5)P2, or localised recruitment of PIP5K to generate PI(4,5)P2.”
From Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane (2020) · cites this paper as [132]
Cites
Veatch, S. L., Machta, B. B., Shelby, S. A., Chiang, E. N., Holowka, D. A., & Baird, B. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031457 · Cited by 290 · see citing works
Schmick, M., Vartak, N., Papke, B., Kovacevic, M., Truxius, D. C., Rossmannek, L., & Bastiaens, P. I. H. (2014) · Cell · doi:10.1016/j.cell.2014.02.051 · Cited by 243 · see citing works
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Phosphatidylinositol(4,5)bisphosphate: diverse functions at the plasma membrane
Katan, M., & Cockcroft, S. (2020) · Essays in Biochemistry · doi:10.1042/ebc20200041 · Cited by 176 · see citing works
- Authors
- Hammond, G. R. V.
- Affiliations
- University of Pittsburgh (US)
- Corresponding author
- Hammond, Gerald R.V.
- ORCID
- Hammond, Gerald R.V.
- Venue
- Biochemical Society Transactions
- Publisher
- Portland Press Ltd.
- Published
- 2016-02-09
- Volume
- 44
- Issue
- 1
- Pages
- 228-233
- ISSN
- 0300-5127 (ISSN-L)
- 1470-8752
- OpenAlex
- W2310769659
- Cited by
- 28
- References
- 2
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 3 · 2023: 1 · 2022: 4 · 2021: 4 · 2020: 5 · 2019: 1 · 2018: 3 · 2017: 3 · 2016: 1
- FWCI
- 0.24
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical Society Transactions (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- phosphatidylinositol 4,5-bisphosphate, plasma membrane, lipid signaling, lipid spatial distribution, lipid metabolism, protein-lipid interactions, second messengers, protein recruitment, lipid cofactors
- MeSH terms
- Animals, Cell Membrane, Humans, Models, Biological, Phosphatidylinositol 4,5-Diphosphate
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