Literature DB >> 8994386

Occurrence of WE-14 and chromogranin A-derived peptides in tissues of the human and bovine gastro-entero-pancreatic system and in human neuroendocrine neoplasia.

C M Gleeson1, W J Curry, C F Johnston, K D Buchanan.   

Abstract

Antisera were generated to the synthetic peptides SREWEDS and KELTAE which correspond to residues 315-321 and 332-337 of human chromogranin A (CgA) respectively. KELTAE represents the C-terminal hexapeptide of WE-14, and SREWEDS (residue 316 human CgA Lys/Arg substitution) represents the C-terminal heptapeptide of the Intervening Peptide, located between pancreastatin and WE-14. The antisera were employed to study the occurrence of WE-14 and CgA-derived peptides in human and bovine gastro-entero-pancreatic (GEP) tissues and in a range of human GEP neuroendocrine tumours. Immunocytochemical analyses of normal human and bovine tissues demonstrated that each antiserum immunostained endocrine cells throughout the GEP tract, Variable intensities of immunostaining were detected in neoplastic tissues. Quantitatively, the highest levels of SREWEDS and KELTAE immunoreactivity were detected in pancreatic extracts, with lower levels in gastrointestinal tissues. Elevated levels of each immunoreactant were detected in neoplastic tissues. Chromatographic analysis resolved several SREWEDS-related peptides and a major KELTAE-related peptide that co-eluted with synthetic human WE-14. The present study has demonstrated that CgA is processed to generate distinct peptide products in normal and neoplastic tissues of the GEP system. A single molecular species co-eluting with synthetic human WE-14 was predominant and consistently detected in all the tissues studied.

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Year:  1996        PMID: 8994386     DOI: 10.1677/joe.0.1510409

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  5 in total

1.  Immunohistochemical evaluation of the post-translational processing of chromogranin A in human pituitary adenomas.

Authors:  A P Heaney; W J Curry; K M Pogue; V L Armstrong; M Mirakhur; B Sheridan; C F Johnston; K D Buchanan; A B Atkinson
Journal:  Pituitary       Date:  2000-10       Impact factor: 4.107

2.  Chromogranin A is an autoantigen in type 1 diabetes.

Authors:  Brian D Stadinski; Thomas Delong; Nichole Reisdorph; Richard Reisdorph; Roger L Powell; Michael Armstrong; Jon D Piganelli; Gene Barbour; Brenda Bradley; Frances Crawford; Philippa Marrack; Sushil K Mahata; John W Kappler; Kathryn Haskins
Journal:  Nat Immunol       Date:  2010-02-07       Impact factor: 25.606

3.  Loss of gut barrier integrity triggers activation of islet-reactive T cells and autoimmune diabetes.

Authors:  Chiara Sorini; Ilaria Cosorich; Marta Lo Conte; Lorena De Giorgi; Federica Facciotti; Roberta Lucianò; Martina Rocchi; Roberto Ferrarese; Francesca Sanvito; Filippo Canducci; Marika Falcone
Journal:  Proc Natl Acad Sci U S A       Date:  2019-06-10       Impact factor: 11.205

4.  Characterization and plasma measurement of the WE-14 peptide in patients with pheochromocytoma.

Authors:  Johann Guillemot; Marlène Guérin; Erwan Thouënnon; Maité Montéro-Hadjadje; Jérôme Leprince; Hervé Lefebvre; Marc Klein; Mihaela Muresan; Youssef Anouar; Laurent Yon
Journal:  PLoS One       Date:  2014-02-11       Impact factor: 3.240

Review 5.  Role and function of granin proteins in diabetes mellitus.

Authors:  Zoltan Herold; Marton Doleschall; Aniko Somogyi
Journal:  World J Diabetes       Date:  2021-07-15
  5 in total

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