P110δ

P110δ
Phosphoinositide-3-kinase, catalytic, delta polypeptide
Identifiers
Symbols PIK3CD; P110DELTA; PI3K; p110D
External IDs OMIM602839 MGI1098211 HomoloGene3686 GeneCards: PIK3CD Gene
EC number 2.7.1.153
RNA expression pattern
PBB GE PIK3CD 203879 at tn.png
PBB GE PIK3CD 211230 s at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 5293 18707
Ensembl ENSG00000171608 ENSMUSG00000039936
UniProt O00329 Q3T9Y0
RefSeq (mRNA) NM_005026 XM_986912
RefSeq (protein) NP_005017 XP_992006
Location (UCSC) Chr 1:
9.71 – 9.79 Mb
Chr 4:
149.02 – 149.08 Mb
PubMed search [1] [2]

Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta isoform also known as phosphoinositide 3-kinase (PI3K) or p110δ is an enzyme that in humans is encoded by the PIK3CD gene.[1][2][3]

p110δ regulates immune function. In contrast to the other class IA PI3Ks p110α and p110β, p110δ is principally expressed in leukocytes (white blood cells). Genetic and pharmacological inactivation of p110δ has revealed that this enzymes is important for the function of T cells, B cell, mast cells and neutrophils. Hence, p110δ is consider to be a promising target for drugs that aim to prevent or treat inflammation and autoimmunity and transplant rejection.[4]

Phosphoinositide 3-kinases (PI3Ks) phosphorylate the 3-prime OH position of the inositol ring of inositol lipids. The class I PI3Ks display a broad phosphoinositide lipid substrate specificity and include p110α, p110β, and p110γ. p110α and p110β interact with SH2/SH3-domain-containing p85 adaptor proteins and with GTP-bound Ras.[3]

Contents

Biochemistry

Like the other class IA PI3Ks, p110δ is a catalytic subunit, whose activity and subcellular localisation are controlled by an associated p85α, p55α, p50α or p85β regulatory subunit. The p55γ regulatory subunit is not thought to be expressed at significant levels in immune cells. These is no evidence for selective association between p110α, p110β or p110δ for any particular regulatory subunit. The class IA regulatory subunits (collectively referred to here as p85) bind to proteins which have been phosphorylated on tyrosines. Tyrosine kinases often operate near the plasma membrane and hence control the recruitment of p110δ to the plasma membrane where it substrate PtdIns(4,5)P2 is found. The conversion of PtdIns(4,5)P2 to PtdIns(3,4,5)P3 triggers signal transduction cascades controlled by PKB (also known as Akt), Tec family kinases, and other proteins that contain PH domains. In immune cells, antigen receptors, cytokine receptors and costimulatory and accessory receptors stimulate tyrosine kinase activity and hence all have the potential to initiate PI3K signalling.[5][6]

Functions

For reasons that are not well understood, p110δ appears to be activated in preference to p110α and p110β in a number of immune cells. The following is a brief summary of the role of p110δ in selected leukocyte subsets.

T cells

In T cells, the antigen receptor (TCR) and costimulatory receptors (CD28 and ICOS) are thought to be main receptors responsible for recruiting and activating p110δ. Genetic inactivation of p110δ in mice causes T cells to be less responsive to antigen as determined by their reduced ability to proliferate and secrete interleukin 2. This may in part results from incomplete assembly of other signalling proteins at the immune synapse. The TCR cannot stimulate the phosphorylation of Akt in that absence of p110δ activity.[7]

B cells

p110δ is a key regulator of B cell proliferation and function. p110δ deficient mice have deficient antibody responses. They also lack to B cell subsets: B1 cells (found in body cavities such as the peritoneum) and marginal zone B cells, found in the periphery of spleen follicles).[7]

Mast cells

p110δ controls mast cell release of the granules responsible for allergic reactions. Thus inhibition of p110δ reduces allergic responses.[8]

Neutrophils

In conjunction with p110γ, p110δ controls the release of reactive oxygen species in neutrophils.[9]

Pharmacology

The US pharmaceutical company ICOS has produced a selective inhibitor of p110δ called IC87114. This inhibitor has been shown to selectively impair B cell, mast cell and neutrophil functions and is therefore a potential immune-modulator.[citation needed]

Another p110δ inhibitor is CAL101 which has reported good results from phase I clinical trials.[10]

Interactions

PIK3CD has been shown to interact with PIK3R1,[1] PIK3CG[1] and PIK3R2.[1]

See also

  • Phosphoinositide 3-kinase inhibitor

References

  1. ^ a b c d Vanhaesebroeck B, Welham MJ, Kotani K, Stein R, Warne PH, Zvelebil MJ, Higashi K, Volinia S, Downward J, Waterfield MD (May 1997). "P110delta, a novel phosphoinositide 3-kinase in leukocytes". Proc Natl Acad Sci U S A 94 (9): 4330–5. doi:10.1073/pnas.94.9.4330. PMC 20722. PMID 9113989. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=20722. 
  2. ^ Seki N, Nimura Y, Ohira M, Saito T, Ichimiya S, Nomura N, Nakagawara A (Feb 1998). "Identification and chromosome assignment of a human gene encoding a novel phosphatidylinositol-3 kinase". DNA Res 4 (5): 355–8. doi:10.1093/dnares/4.5.355. PMID 9455486. 
  3. ^ a b "Entrez Gene: PIK3CD phosphoinositide-3-kinase, catalytic, delta polypeptide". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5293. 
  4. ^ Harris SJ, Foster JG, Ward SG (November 2009). "PI3K isoforms as drug targets in inflammatory diseases: lessons from pharmacological and genetic strategies". Curr Opin Investig Drugs 10 (11): 1151–62. PMID 19876783. 
  5. ^ Okkenhaug K, Vanhaesebroeck B (April 2003). "PI3K in lymphocyte development, differentiation and activation". Nat. Rev. Immunol. 3 (4): 317–30. doi:10.1038/nri1056. PMID 12669022. 
  6. ^ Deane JA, Fruman DA (2004). "Phosphoinositide 3-kinase: diverse roles in immune cell activation". Annu. Rev. Immunol. 22: 563–98. doi:10.1146/annurev.immunol.22.012703.104721. PMID 15032589. 
  7. ^ a b Okkenhaug K, Bilancio A, Farjot G, Priddle H, Sancho S, Peskett E, Pearce W, Meek SE, Salpekar A, Waterfield MD, Smith AJ, Vanhaesebroeck B (August 2002). "Impaired B and T cell antigen receptor signaling in p110delta PI 3-kinase mutant mice". Science 297 (5583): 1031–4. doi:10.1126/science.1073560. PMID 12130661. 
  8. ^ Ali K, Bilancio A, Thomas M, Pearce W, Gilfillan AM, Tkaczyk C, Kuehn N, Gray A, Giddings J, Peskett E, Fox R, Bruce I, Walker C, Sawyer C, Okkenhaug K, Finan P, Vanhaesebroeck B (October 2004). "Essential role for the p110delta phosphoinositide 3-kinase in the allergic response". Nature 431 (7011): 1007–11. doi:10.1038/nature02991. PMID 15496927. 
  9. ^ Condliffe AM, Davidson K, Anderson KE, Ellson CD, Crabbe T, Okkenhaug K, Vanhaesebroeck B, Turner M, Webb L, Wymann MP, Hirsch E, Ruckle T, Camps M, Rommel C, Jackson SP, Chilvers ER, Stephens LR, Hawkins PT (August 2005). "Sequential activation of class IB and class IA PI3K is important for the primed respiratory burst of human but not murine neutrophils". Blood 106 (4): 1432–40. doi:10.1182/blood-2005-03-0944. PMID 15878979. 
  10. ^ "Calistoga Pharmaceuticals presents CAL-101 PI3K inhibitor data at European Hematology Association Congress". News-Medical.Net. 2010-06 -14. http://www.news-medical.net/news/20100614/Calistoga-Pharmaceuticals-presents-CAL-101-PI3K-inhibitor-data-at-European-Hematology-Association-Congress.aspx. 

Further reading


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