Beta cell expression of endogenous xenotropic retrovirus distinguishes diabetes-susceptible NOD/Lt from resistant NON/Lt mice

H. Rex Gaskins, Michal Prochazka, Kazuyuki Hamaguchi, David V. Serreze, Edward H. Leiter

Research output: Contribution to journalArticle

Abstract

Endogeneous retroviral expression in β cells is a feature of prediabetes in nonobese diabetic (NOD) mice. The purpose of this study was to characterize the class-specific pattern of retroviral gene expression in NOD/Lt β cells versus a related, but diabetes-resistant strain, NON/Lt. Electron microscopic comparison of β cells from both strains indicated low constitutive expression of the intracisternal type A (IAP) retroviral class. However, NOD β cells, in contrast to NON β cells, expressed an additional intracisternal retroviral form resembling a type C particle. Antibodies against both IAP and type C were detected in NOD, with the humoral response to type C, but not IAP, preceding decline in β cell function. RNA was extracted from freshly isolated islets from NOD and NON males. Comparative Northern blot analysis of total type C retroviral gene expression using a gag-pol DNA probe corroborated expression of endogenous type C proviruses in both NOD and NON islet cells and thymus. Use of class-specific retroviral probes identified the class of expressed endogenous retrovirus distinguishing the two inbred strains. The single ecotropic provirus present in both the NOD and NON genome (Emv-30) was not expressed in islets or thymus of either strain. Comparison of endogenous xenotropic provirus content by Southern blot analysis revealed two unique xenotropic loci (Xmv-65, -66) in NOD; 8.4 and 3.0 kb xenotropic envelope (env) RNA transcripts were detected in NOD, but not NON islets and thymus. NON contained three xenotropic loci common to other inbred strains (Xmv-21, -25, and -28). Both strains were partially characterized for content of recombinant (polytropic and modified polytropic) proviruses. IAP RNA expression was common to both NOD and NON islets and hence could not be specifically asso-ciated with the unique intracisternal type C particle found in NOD, but not NON β cells. In conclusion, this study shows that expression of xenotropic type C but not IAP distinguishes retroviral activity in NOD/Lt versus NON/Lt β cells. The potential pathogenic role of retroviral gene expression in NOD β cells is discussed.

Original languageEnglish (US)
Pages (from-to)2220-2227
Number of pages8
JournalJournal of Clinical Investigation
Volume90
Issue number6
DOIs
StatePublished - Dec 1992

Fingerprint

Endogenous Retroviruses
Proviruses
Thymus Gland
RNA
Gene Expression
Prediabetic State
Inbred NOD Mouse
DNA Probes
Southern Blotting
Islets of Langerhans
Northern Blotting
Genome
Electrons

Keywords

  • Diabetes
  • Endogenous retrovirus
  • Mice
  • Nonobese diabetic
  • β cell

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Beta cell expression of endogenous xenotropic retrovirus distinguishes diabetes-susceptible NOD/Lt from resistant NON/Lt mice. / Gaskins, H. Rex; Prochazka, Michal; Hamaguchi, Kazuyuki; Serreze, David V.; Leiter, Edward H.

In: Journal of Clinical Investigation, Vol. 90, No. 6, 12.1992, p. 2220-2227.

Research output: Contribution to journalArticle

Gaskins, H. Rex ; Prochazka, Michal ; Hamaguchi, Kazuyuki ; Serreze, David V. ; Leiter, Edward H. / Beta cell expression of endogenous xenotropic retrovirus distinguishes diabetes-susceptible NOD/Lt from resistant NON/Lt mice. In: Journal of Clinical Investigation. 1992 ; Vol. 90, No. 6. pp. 2220-2227.
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AU - Serreze, David V.

AU - Leiter, Edward H.

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N2 - Endogeneous retroviral expression in β cells is a feature of prediabetes in nonobese diabetic (NOD) mice. The purpose of this study was to characterize the class-specific pattern of retroviral gene expression in NOD/Lt β cells versus a related, but diabetes-resistant strain, NON/Lt. Electron microscopic comparison of β cells from both strains indicated low constitutive expression of the intracisternal type A (IAP) retroviral class. However, NOD β cells, in contrast to NON β cells, expressed an additional intracisternal retroviral form resembling a type C particle. Antibodies against both IAP and type C were detected in NOD, with the humoral response to type C, but not IAP, preceding decline in β cell function. RNA was extracted from freshly isolated islets from NOD and NON males. Comparative Northern blot analysis of total type C retroviral gene expression using a gag-pol DNA probe corroborated expression of endogenous type C proviruses in both NOD and NON islet cells and thymus. Use of class-specific retroviral probes identified the class of expressed endogenous retrovirus distinguishing the two inbred strains. The single ecotropic provirus present in both the NOD and NON genome (Emv-30) was not expressed in islets or thymus of either strain. Comparison of endogenous xenotropic provirus content by Southern blot analysis revealed two unique xenotropic loci (Xmv-65, -66) in NOD; 8.4 and 3.0 kb xenotropic envelope (env) RNA transcripts were detected in NOD, but not NON islets and thymus. NON contained three xenotropic loci common to other inbred strains (Xmv-21, -25, and -28). Both strains were partially characterized for content of recombinant (polytropic and modified polytropic) proviruses. IAP RNA expression was common to both NOD and NON islets and hence could not be specifically asso-ciated with the unique intracisternal type C particle found in NOD, but not NON β cells. In conclusion, this study shows that expression of xenotropic type C but not IAP distinguishes retroviral activity in NOD/Lt versus NON/Lt β cells. The potential pathogenic role of retroviral gene expression in NOD β cells is discussed.

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