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Phospholipase C

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Phospholipase C (PLC) is a class of membrane-associated enzymes that cleave phospholipids just before the phosphate group (see figure). It is most commonly taken to be synonymous with the human forms of this enzyme, which play an important role in eukaryotic cell physiology, in particular signal transduction pathways. Phospholipase C's role in signal transduction is its cleavage of phosphatidylinositol 4,5-bisphosphate (PIP2) into diacyl glycerol (DAG) and inositol 1,4,5-trisphosphate (IP3), which serve as second messengers. Activators of each PLC vary, but typically include heterotrimeric G protein subunits, protein tyrosine kinases, small G proteins, Ca2+, and phospholipids.[1]

Cleavage sites of phospholipases. Phospholipase C enzymes cut just before the phosphate attached to the R3 moiety.

There are thirteen kinds of mammalian phospholipase C that are classified into six isotypes (β, γ, δ, ε, ζ, η) according to structure. Each PLC has unique and overlapping controls over expression and subcellular distribution. However, PLC is not limited to mammals, and is present in bacteria and Chromadorea as well.

Phospholipase C
Identifiers
EC no.3.1.4.3
CAS no.9001-86-9
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Variants

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Mammalian variants

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The extensive number of functions exerted by the PLC reaction requires that it be strictly regulated and able to respond to multiple extra- and intracellular inputs with appropriate kinetics. This need has guided the evolution of six isotypes of PLC in animals, each with a distinct mode of regulation. The pre-mRNA of PLC can also be subject to differential splicing such that a mammal may have up to 30 PLC enzymes.[2]

Bacterial variants

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Most of the bacterial variants of phospholipase C are characterized into one of four groups of structurally related proteins. The toxic phospholipases C are capable of interacting with eukaryotic cell membranes and hydrolyzing phosphatidylcholine and sphingomyelin, leading to cell lysis.[3]

Chromadorea

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The class of Chromadorea also utilizes the enzyme phospholipase C to regulate the releases of calcium. The enzyme releases inositol 1,4,5-trisphosphate (IP3) that denotes a signaling pathway involved in activating ovulation, the propelling of the oocyte into the spermatheca. This gene is involved in various activities like controlling GTPase, breaking down certain molecules, and binding to small GTPase. It helps in fighting bacteria and regulating protein movement in cells. It's found in the excretory system, intestines, nerves, and reproductive organs. The expression of the enzyme in the spermatheca is controlled by the transcription factors FOS-1 and JUN-1.[4]

Enzyme structure

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Comparison of C2 domain of mammalian PI-PLC in red and C2-like domain of Bacillus cereus in cyan

In mammals, PLCs share a conserved core structure and differ in other domains specific to each family. The core enzyme includes a split triosephosphate isomerase (TIM) barrel, pleckstrin homology (PH) domain, four tandem EF hand domains, and a C2 domain.[1] The TIM barrel contains the active site, all catalytic residues, and a Ca2+ binding site. It has an autoinhibitory insert that interrupts its activity called an X-Y linker. The X-Y linker has been shown to occlude the active site, and with its removal, PLC is activated.[5]

The genes encoding alpha-toxin (Clostridium perfringens), Bacillus cereus PLC (BC-PLC), and PLCs from Clostridium bifermentans and Listeria monocytogenes have been isolated and nucleotides sequenced. The sequences have significant homology, approximately 250 residues, from the N-terminus. Alpha-toxin has an additional 120 residues in the C-terminus. The C-terminus of the alpha-toxin has been reported as a "C2-like" domain, referencing the C2 domain found in eukaryotes that are involved in signal transduction and present in mammalian phosphoinositide phospholipase C.[6]

Enzyme mechanism

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General reaction catalyzed by phospholipase C

The primary catalyzed reaction of PLC occurs on an insoluble substrate at a lipid-water interface. The residues in the active site are conserved in all PLC isotypes. In animals, PLC selectively catalyzes the hydrolysis of the phospholipid phosphatidylinositol 4,5-bisphosphate (PIP2) on the glycerol side of the phosphodiester bond. There is the formation of a weakly enzyme-bound intermediate, inositol 1,2-cyclic phosphodiester, and release of diacylglycerol (DAG). The intermediate is then hydrolyzed to inositol 1,4,5-trisphosphate (IP3).[7] Thus the two end products are DAG and IP3. The acid/base catalysis requires two conserved histidine residues and a Ca2+ ion is needed for PIP2 hydrolysis. It has been observed that the active-site Ca2+ coordinates with four acidic residues and if any of the residues are mutated then a greater Ca2+ concentration is needed for catalysis.[8]

Signaling Pathway

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Phosphoinositide-specific phospholipase C (PLC) is a key player in cell signaling processes. When cells encounter signals like hormones or growth factors, PLC breaks down a molecule called PIP2 to produce new signaling molecules. PIP2 is a type of molecule found in cell membranes. When cells receive certain signals from outside, an enzyme called PLC breaks down PIP2 into smaller molecules, which then send messages within the cell. Various types of PLC are activated differently, contributing to cells' ability to respond to their surroundings.

Regulation

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Activation

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Receptors that activate this pathway are mainly G protein-coupled receptors coupled to the Gαq subunit, including:

Other, minor, activators than Gαq are:

Inhibition

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  • Small molecule U73122: aminosteroid, putative PLC inhibitor.[11][12] However, the specificity of U73122 has been questioned.[13] It has been reported that U73122 activates the phospholipase activity of purified PLCs.[14]
  • Edelfosine: lipid-like, anti-neoplastic agent (ET-18-OCH3)[15]
  • Autoinhibition of the X-Y linker in mammalian cells: It is proposed that the X-Y linker consists of long stretches of acidic amino acids that form dense areas of negative charge. These areas could be repelled by the negatively charged membrane upon binding of the PLC to membrane lipids. The combination of repulsion and steric constraints is thought to remove the X-Y linker from near the active site and relieve auto-inhibition.[1]
  • Compounds containing the morpholinobenzoic acid scaffold belong to a class of drug-like phosphatidylcholine-specific PLC inhibitors.[16][17][18]
  • o-phenanthroline: heterocyclic organic compound, known to inhibit zinc-metalloenzymes[19]
  • EDTA: molecule that chelates Zn2+ ions and effectively inactivates PLC, known to inhibit zinc-metalloenzymes[20]

Biological function

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PLC mediated cleavage of PIP2 to DAG and IP3

PLC cleaves the phospholipid phosphatidylinositol 4,5-bisphosphate (PIP2) into diacyl glycerol (DAG) and inositol 1,4,5-trisphosphate (IP3). Thus PLC has a profound impact on the depletion of PIP2, which acts as a membrane anchor or allosteric regulator and an agonist for many lipid-gated ion channels.[21][22] PIP2 also acts as the substrate for synthesis of the rarer lipid phosphatidylinositol 3,4,5-trisphosphate (PIP3), which is responsible for signaling in multiple reactions.[23] Therefore, PIP2 depletion by the PLC reaction is critical to the regulation of local PIP3 concentrations both in the plasma membrane and the nuclear membrane.

The two products of the PLC catalyzed reaction, DAG and IP3, are important second messengers that control diverse cellular processes and are substrates for synthesis of other important signaling molecules. When PIP2 is cleaved, DAG remains bound to the membrane, and IP3 is released as a soluble structure into the cytosol. IP3 then diffuses through the cytosol to bind to IP3 receptors, particularly calcium channels in the smooth endoplasmic reticulum (ER). This causes the cytosolic concentration of calcium to increase, causing a cascade of intracellular changes and activity.[24] In addition, calcium and DAG together work to activate protein kinase C, which goes on to phosphorylate other molecules, leading to altered cellular activity.[24] End-effects include taste, tumor promotion, as well as vesicle exocytosis, superoxide production from NADPH oxidase, and JNK activation.[24][25]

Both DAG and IP3 are substrates for the synthesis of regulatory molecules. DAG is the substrate for the synthesis of phosphatidic acid, a regulatory molecule. IP3 is the rate-limiting substrate for the synthesis of inositol polyphosphates, which stimulate multiple protein kinases, transcription, and mRNA processing.[26] Regulation of PLC activity is thus vital to the coordination and regulation of other enzymes of pathways that are central to the control of cellular physiology.

Further information: Calcium function in vertebrates and Function of protein kinase C

Additionally, phospholipase C plays an important role in the inflammation pathway. The binding of agonists such as thrombin, epinephrine, or collagen, to platelet surface receptors can trigger the activation of phospholipase C to catalyze the release of arachidonic acid from two major membrane phospholipids, phosphatidylinositol and phosphatidylcholine. Arachidonic acid can then go on into the cyclooxygenase pathway (producing prostoglandins (PGE1, PGE2, PGF2), prostacyclins (PGI2), or thromboxanes (TXA2)), and the lipoxygenase pathway (producing leukotrienes (LTB4, LTC4, LTD4, LTE4)).[27]

The bacterial variant Clostridium perfringens type A produces alpha-toxin. The toxin has phospholipase C activity, and causes hemolysis, lethality, and dermonecrosis. At high concentrations, alpha-toxin induces massive degradation of phosphatidylcholine and sphingomyelin, producing diacylglycerol and ceramide, respectively. These molecules then participate in signal transduction pathways.[6] It has been reported that the toxin activates the arachidonic acid cascade in isolated rat aorta.[28] The toxin-induced contraction was related to generation of thromboxane A2 from arachidonic acid. Thus it is likely the bacterial PLC mimics the actions of endogenous PLC in eukaryotic cell membranes.

See also

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References

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  1. ^ a b c Kadamur G, Ross EM (2013). "Mammalian phospholipase C". Annual Review of Physiology. 75: 127–54. doi:10.1146/annurev-physiol-030212-183750. PMID 23140367.
  2. ^ Suh, PG; Park, JI; Manzoli, L; Cocco, L; Peak, JC; Katan, M; Fukami, K; Kataoka, T; Yun, S; Ryu, SH (2008). "Multiple roles of phosphoinositide-specific phospholipase C isozymes". BMB Reports. 41 (6): 415–34. doi:10.5483/bmbrep.2008.41.6.415. hdl:11585/62661. PMID 18593525.
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  5. ^ Hicks SN, Jezyk MR, Gershburg S, Seifert JP, Harden TK, Sondek J (August 2008). "General and versatile autoinhibition of PLC isozymes". Molecular Cell. 31 (3): 383–94. doi:10.1016/j.molcel.2008.06.018. PMC 2702322. PMID 18691970.
  6. ^ a b Sakurai J, Nagahama M, Oda M (November 2004). "Clostridium perfringens alpha-toxin: characterization and mode of action". Journal of Biochemistry. 136 (5): 569–74. doi:10.1093/jb/mvh161. PMID 15632295.
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  9. ^ a b Walter F. Boron (2003). Medical Physiology: A Cellular And Molecular Approaoch. Elsevier/Saunders. p. 1300. ISBN 978-1-4160-2328-9. Page 104
  10. ^ GeneGlobe -> GHRH Signaling[permanent dead link‍] Retrieved on May 31, 2009
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  15. ^ Horowitz LF, Hirdes W, Suh BC, Hilgemann DW, Mackie K, Hille B (September 2005). "Phospholipase C in living cells: activation, inhibition, Ca2+ requirement, and regulation of M current". The Journal of General Physiology. 126 (3): 243–62. doi:10.1085/jgp.200509309. PMC 2266577. PMID 16129772.
  16. ^ Rees, Shaun W. P.; Leung, Euphemia; Reynisson, Jóhannes; Barker, David; Pilkington, Lisa I. (2021-09-01). "Development of 2-Morpholino-N-hydroxybenzamides as anti-proliferative PC-PLC inhibitors". Bioorganic Chemistry. 114: 105152. doi:10.1016/j.bioorg.2021.105152. ISSN 0045-2068. PMID 34328856.
  17. ^ Eurtivong, C.; Pilkington, L. I.; van Rensburg, M.; White, R. M.; Kaur Brar, H.; Rees, S.; Paulin, E. K.; Xu, C. S.; Sharma, N.; Leung, I. K. H.; Leung, E.; Barker, D.; Reynisson, J. (1 February 2020). "Discovery of novel phosphatidylcholine-specific phospholipase C drug-like inhibitors as potential anticancer agents". European Journal of Medicinal Chemistry. 187: 111919. doi:10.1016/j.ejmech.2019.111919. PMID 31810783. S2CID 208813280.
  18. ^ Pilkington, L. I.; Sparrow, K.; Rees, S. W. P.; Paulin, E. K.; van Rensburg, M.; Xu, C. S.; Langley, R. J.; Leung, I. K. H.; Reynisson, J.; Leung, E.; Barker, D. (2020). "Development, Synthesis and Biological Investigation of a Novel Class of Potent PC-PLC Inhibitors". European Journal of Medicinal Chemistry. 191: 112162. doi:10.1016/j.ejmech.2020.112162. PMID 32101781. S2CID 211536972.
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  20. ^ "Phospholipase C, Phosphatidylinositol-specific from Bacillus cereus" (PDF). Product Information. Sigma Aldrich.
  21. ^ Hilgemann DW (October 2007). "Local PIP(2) signals: when, where, and how?". Pflügers Archiv. 455 (1): 55–67. doi:10.1007/s00424-007-0280-9. PMID 17534652. S2CID 29839094.
  22. ^ Hansen (1 May 2015). "Lipid agonism: The PIP2 paradigm of ligand-gated ion channels". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1851 (5): 620–628. doi:10.1016/j.bbalip.2015.01.011. PMC 4540326. PMID 25633344.
  23. ^ Falkenburger BH, Jensen JB, Dickson EJ, Suh BC, Hille B (September 2010). "Phosphoinositides: lipid regulators of membrane proteins". The Journal of Physiology. 588 (Pt 17): 3179–85. doi:10.1113/jphysiol.2010.192153. PMC 2976013. PMID 20519312.
  24. ^ a b c Alberts B, Lewis J, Raff M, Roberts K, Walter P (2002). Molecular biology of the cell (4th ed.). New York: Garland Science. ISBN 978-0-8153-3218-3.
  25. ^ Li Z, Jiang H, Xie W, Zhang Z, Smrcka AV, Wu D (February 2000). "Roles of PLC-beta2 and -beta3 and PI3Kgamma in chemoattractant-mediated signal transduction". Science. 287 (5455): 1046–9. Bibcode:2000Sci...287.1046L. doi:10.1126/science.287.5455.1046. PMID 10669417.
  26. ^ Gresset A, Sondek J, Harden TK (2012). "The phospholipase C isozymes and their regulation". Phosphoinositides I: Enzymes of Synthesis and Degradation. Subcellular Biochemistry. Vol. 58. pp. 61–94. doi:10.1007/978-94-007-3012-0_3. ISBN 978-94-007-3011-3. PMC 3638883. PMID 22403074.
  27. ^ Piomelli, Daniele (1993-04-01). "Arachidonic acid in cell signaling" (PDF). Current Opinion in Cell Biology. 5 (2): 274–280. doi:10.1016/0955-0674(93)90116-8. PMID 7685181.
  28. ^ Fujii Y, Sakurai J (May 1989). "Contraction of the rat isolated aorta caused by Clostridium perfringens alpha toxin (phospholipase C): evidence for the involvement of arachidonic acid metabolism". British Journal of Pharmacology. 97 (1): 119–24. doi:10.1111/j.1476-5381.1989.tb11931.x. PMC 1854495. PMID 2497921.
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