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Peli: a family of signal-responsive E3 ubiquitin ligases mediating TLR signaling and T-cell tolerance 被引量:3

Peli: a family of signal-responsive E3 ubiquitin ligases mediating TLR signaling and T-cell tolerance
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摘要 E3 ubiquitin ligases play a crucial role in regulating immune receptor signaling and modulating immune homeostasis and activation. One emerging family of such E3s is the Pelle-interacting (Peli) proteins, characterized by the presence of a cryptic forkhead-associated domain involved in substrate binding and an atypical RING domain mediating formation of both lysine (K) 63- and K48-1inked polyubiquitin chains. A well-recognized function of Peli family members is participation in the signal transduction mediated by Toll-like receptors (TLRs) and IL-1 receptor. Recent gene targeting studies have provided important insights into the in vivofunctions of Pelil in the regulation of TLR signaling and inflammation. These studies have also extended the biological functions of Pelil to the regulation of T-cell tolerance. Consistent with its immunoregulatory functions, Peli I responds to different immune stimuli for its gene expression and catalytic activation. In this review, we discuss the recent progress, as well as the historical perspectives in the regulation and biological functions of Peli. E3 ubiquitin ligases play a crucial role in regulating immune receptor signaling and modulating immune homeostasis and activation. One emerging family of such E3s is the Pelle-interacting (Peli) proteins, characterized by the presence of a cryptic forkhead-associated domain involved in substrate binding and an atypical RING domain mediating formation of both lysine (K) 63- and K48-1inked polyubiquitin chains. A well-recognized function of Peli family members is participation in the signal transduction mediated by Toll-like receptors (TLRs) and IL-1 receptor. Recent gene targeting studies have provided important insights into the in vivofunctions of Pelil in the regulation of TLR signaling and inflammation. These studies have also extended the biological functions of Pelil to the regulation of T-cell tolerance. Consistent with its immunoregulatory functions, Peli I responds to different immune stimuli for its gene expression and catalytic activation. In this review, we discuss the recent progress, as well as the historical perspectives in the regulation and biological functions of Peli.
出处 《Cellular & Molecular Immunology》 SCIE CAS CSCD 2012年第2期113-122,共10页 中国免疫学杂志(英文版)
关键词 Peli Pellino UBIQUITINATION NF-KB TLR T-cell tolerance Peli Pellino ubiquitination NF-kB TLR T-cell tolerance
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  • 1Wilkes MC, Mitchell H, Penheiter SG, et al. Transforming growth factor-{beta} activation ofphosphatidylinositol 3-kinase is independent of Smad2 and Smad3 and regulates fibroblast responses via p21-activated kinase-2. Cancer Res 2005; 65:10431- 10440.
  • 2Chow JY, Quach KT, Cabrera BL, Cabral JA, Beck SE, Carethers JM. RASPERK modulates TGFbeta-regulated PTEN expression in human pancreatic adenocarcinoma cells. Carcinogenesis 2007; 28:2321-2327.
  • 3Vogelmann R, Nguyen-Tat MD, Giehl K, Adler G, Wedlich D,Menke A. TGFbeta-induced downregulation of E-cadherin-based cell-cell adhesion depends on PI3-kinase and PTEN. J Cell Sci 2005; 118:4901-4912.
  • 4Valderrama-Carvajal H, Cocolakis E, Lacerte A, et al. Activin/ TGF-beta induce apoptosis through Smad-dependent expression of the lipid phosphatase SHIE Nat Cell Biol 2002; 4:963-969.
  • 5He XC, Zhang J, Tong WG, et al. BMP signaling inhibits intestinal stem cell self-renewal through suppression of Wnt-betacatenin signaling. Nat Genet 2004; 36:1117-1121.
  • 6Tian Q, He XC, Hood L, Li L. Bridging the BMP and Wnt pathways by PI3 kinase/Akt and 14-3-3zeta. Cell Cycle 2005; 4:215-216.
  • 7Waite KA, Eng C. BMP2 exposure results in decreased PTEN protein degradation and increased PTEN levels. Hum Mol Genet 2003; 12:679-684.
  • 8Beck SE, Carethers JM. BMP suppresses PTEN expression via RAS/ERK signaling. Cancer Biol Ther 2007; 6:1313-1317.
  • 9Haramis A-PG, Begthel H, van den Born M, et al. De novo crypt formation and juvenile polyposis on BMP inhibition in mouse intestine. Science 2004; 3113:1684-1686.
  • 10Cadigan KM, Nusse R. Wnt signaling: a common theme in animal development. Genes Dev 1997; 11:3286-3305.

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