Literature DB >> 19550073

Expression and function of IA-2 family proteins, unique neuroendocrine-specific protein-tyrosine phosphatases.

Seiji Torii1.   

Abstract

IA-2 (also known as islet cell antigen ICA-512) and IA-2 beta (also known as phogrin, phosphatase homologue in granules of insulinoma) are major autoantigens in insulin-dependent diabetes mellitus (IDDM). Autoantibodies against both proteins are expressed years before clinical onset, and they become predictive markers for high-risk subjects. However, the role of these genes in the IDDM pathogenesis has been reported fairly negative by recent studies. IA-2 and IA-2 beta are type I transmembrane proteins that possess one inactive protein-tyrosine phosphatase (PTP) domain in the cytoplasmic region, and act as one of the constituents of regulated secretory pathways in various neuroendocrine cell types including pancreatic beta-cells. Existence of IA-2 homologues in different species suggests a fundamental role in neuroendocrine function. Studies of knockout animals have shown their involvement in maintaining hormone content, however, their specific steps in the secretory pathway IA-2 functions as well as their molecular mechanisms in the hormone content regulation are still unknown. More recent studies have suggested a novel function showing that they contribute to pancreatic beta-cell growth. This review attempts to show the possible biological functions of IA-2 family, focusing on their expression and localization in the neuroendocrine cells.

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Year:  2009        PMID: 19550073     DOI: 10.1507/endocrj.k09e-157

Source DB:  PubMed          Journal:  Endocr J        ISSN: 0918-8959            Impact factor:   2.349


  20 in total

Review 1.  Protein phosphatases in pancreatic islets.

Authors:  Henrik Ortsäter; Nina Grankvist; Richard E Honkanen; Åke Sjöholm
Journal:  J Endocrinol       Date:  2014-03-28       Impact factor: 4.286

2.  Aberrant Expression of proPTPRN2 in Cancer Cells Confers Resistance to Apoptosis.

Authors:  Alexey V Sorokin; Binoj C Nair; Yongkun Wei; Kathryn E Aziz; Valentina Evdokimova; Mien-Chie Hung; Junjie Chen
Journal:  Cancer Res       Date:  2015-04-15       Impact factor: 12.701

3.  The pseudophosphatase MK-STYX interacts with G3BP and decreases stress granule formation.

Authors:  Shantá D Hinton; Michael P Myers; Vincent R Roggero; Lizabeth A Allison; Nicholas K Tonks
Journal:  Biochem J       Date:  2010-04-14       Impact factor: 3.857

4.  Stability of proICA512/IA-2 and its targeting to insulin secretory granules require β4-sheet-mediated dimerization of its ectodomain in the endoplasmic reticulum.

Authors:  Juha M Torkko; M Evangelina Primo; Ronald Dirkx; Anne Friedrich; Antje Viehrig; Elisa Vergari; Barbara Borgonovo; Anke Sönmez; Carolin Wegbrod; Martina Lachnit; Carla Münster; Mauricio P Sica; Mario R Ermácora; Michele Solimena
Journal:  Mol Cell Biol       Date:  2015-01-05       Impact factor: 4.272

Review 5.  The pathogenesis and natural history of type 1 diabetes.

Authors:  Mark A Atkinson
Journal:  Cold Spring Harb Perspect Med       Date:  2012-11-01       Impact factor: 6.915

Review 6.  Protein tyrosine phosphatases as wardens of STAT signaling.

Authors:  Frank-D Böhmer; Karlheinz Friedrich
Journal:  JAKSTAT       Date:  2014-02-20

7.  ICA512 RESP18 homology domain is a protein-condensing factor and insulin fibrillation inhibitor.

Authors:  Pamela L Toledo; Juha M Torkko; Andreas Müller; Carolin Wegbrod; Anke Sönmez; Michele Solimena; Mario R Ermácora
Journal:  J Biol Chem       Date:  2019-04-12       Impact factor: 5.157

8.  X-ray structure of the mature ectodomain of phogrin.

Authors:  Martín E Noguera; María E Primo; Jean Jakoncic; Edgardo Poskus; Michele Solimena; Mario R Ermácora
Journal:  J Struct Funct Genomics       Date:  2014-11-26

Review 9.  Islet autoantigens: structure, function, localization, and regulation.

Authors:  Peter Arvan; Massimo Pietropaolo; David Ostrov; Christopher J Rhodes
Journal:  Cold Spring Harb Perspect Med       Date:  2012-08-01       Impact factor: 6.915

10.  The pseudophosphatase phogrin enables glucose-stimulated insulin signaling in pancreatic β cells.

Authors:  Seiji Torii; Chisato Kubota; Naoya Saito; Ayumi Kawano; Ni Hou; Masaki Kobayashi; Ryoko Torii; Masahiro Hosaka; Tadahiro Kitamura; Toshiyuki Takeuchi; Hiroshi Gomi
Journal:  J Biol Chem       Date:  2018-02-26       Impact factor: 5.157

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