Literature DB >> 8971019

Late virus replication events in microglia are required for neurovirulent retrovirus-induced spongiform neurodegeneration: evidence from neural progenitor-derived chimeric mouse brains.

W P Lynch1, E Y Snyder, L Qualtiere, J L Portis, A H Sharpe.   

Abstract

CasBrE is a neurovirulent murine retrovirus which induces a spongiform myeloencephalopathy in susceptible mice. Genetic mapping studies have indicated that sequences responsible for neurovirulence reside within the env gene. To address the question of direct envelope protein neuroxicity in the central nervous system (CNS), we have generated chimeric mice expressing the CasBrE envelope protein in cells of neuroectodermal origin. Specifically, the multipotent neural progenitor cell line C17.2 was engineered to express the CasBrE env gene as either gp70/p15E (CasE) or gp70 alone (CasES). CasE expression in these cells resulted in complete (>10(5)) interference of superinfection with Friend murine leukemia virus clone FB29, whereas CasES expression resulted in a 1.8-log-unit decrease in FB29 titer. Introduction of these envelope-expressing C17.2 cells into the brains of highly susceptible IRW mice resulted in significant engraftment as integral cytoarchitecturally correct components of the CNS. Despite high-level envelope protein expression from the engrafted cells, no evidence of spongiform neurodegeneration was observed. To examine whether early virus replication events were necessary for pathogenesis, C17.2 cells expressing whole virus were transplanted into mice in which virus replication in the host was specifically restricted by Fv-1 to preintegration events. Again, significant C17.2 cell engraftment and infectious virus expression failed to precipitate spongiform lesions. In contrast, transplantation of virus-expressing C17.2 progenitor cells in the absence of the Fv-1 restriction resulted in extensive spongiform neurodegeneration by 2 weeks postengraftment. Cytological examination indicated that infection had spread beyond the engrafted cells, and in particular to host microglia. Spongiform neuropathology in these animals was directly correlated with CasBrE env expression in microglia rather than expression from neural progenitor cells. These results suggest that the envelope protein of CasBrE is not itself neurotoxic but that virus infectious events beyond binding and fusion in microglia are necessary for the induction of CNS disease.

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Year:  1996        PMID: 8971019      PMCID: PMC190987     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  57 in total

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Journal:  J Virol       Date:  1985-05       Impact factor: 5.103

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Journal:  J Virol       Date:  1984-11       Impact factor: 5.103

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Journal:  J Virol       Date:  1985-12       Impact factor: 5.103

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Journal:  J Virol       Date:  1986-07       Impact factor: 5.103

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Authors:  P Jolicoeur; E Rassart
Journal:  J Virol       Date:  1981-02       Impact factor: 5.103

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Authors:  M Czub; F J McAtee; J L Portis
Journal:  J Virol       Date:  1992-06       Impact factor: 5.103

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  21 in total

1.  Neural stem cells as engraftable packaging lines can mediate gene delivery to microglia: evidence from studying retroviral env-related neurodegeneration.

Authors:  W P Lynch; A H Sharpe; E Y Snyder
Journal:  J Virol       Date:  1999-08       Impact factor: 5.103

2.  Rebound from Inhibition: Self-Correction against Neurodegeneration?

Authors:  Shobhana Sivaramakrishnan; William P Lynch
Journal:  J Clin Cell Immunol       Date:  2017-03-13

3.  Brain infection by neuroinvasive but avirulent murine oncornaviruses.

Authors:  S Asković; F J McAtee; C Favara; J L Portis
Journal:  J Virol       Date:  2000-01       Impact factor: 5.103

4.  Postinhibitory rebound neurons and networks are disrupted in retrovirus-induced spongiform neurodegeneration.

Authors:  Ying Li; Robert A Davey; Shobhana Sivaramakrishnan; William P Lynch
Journal:  J Neurophysiol       Date:  2014-05-14       Impact factor: 2.714

5.  Abundant defective viral particles budding from microglia in the course of retroviral spongiform encephalopathy.

Authors:  R Hansen; S Czub; E Werder; J Herold; G Gosztonyi; H Gelderblom; S Schimmer; S Mazgareanu; V ter Meulen; M Czub
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

6.  Neurologic disease induced by polytropic murine retroviruses: neurovirulence determined by efficiency of spread to microglial cells.

Authors:  S J Robertson; K J Hasenkrug; B Chesebro; J L Portis
Journal:  J Virol       Date:  1997-07       Impact factor: 5.103

Review 7.  Differential glycosylation of the Cas-Br-E env protein is associated with retrovirus-induced spongiform neurodegeneration.

Authors:  W P Lynch; A H Sharpe
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

8.  The Evolution of Stem Cells, Disease Modeling, and Drug Discovery for Neurological Disorders.

Authors:  Cameron Pernia; Brian T D Tobe; Ryan O'Donnell; Evan Y Snyder
Journal:  Stem Cells Dev       Date:  2020-05-06       Impact factor: 3.272

9.  Increased expression of MIP-1 alpha and MIP-1 beta mRNAs in the brain correlates spatially and temporally with the spongiform neurodegeneration induced by a murine oncornavirus.

Authors:  S Askovic; C Favara; F J McAtee; J L Portis
Journal:  J Virol       Date:  2001-03       Impact factor: 5.103

10.  Disparate regions of envelope protein regulate syncytium formation versus spongiform encephalopathy in neurological disease induced by murine leukemia virus TR.

Authors:  Samuel L Murphy; Marek J Honczarenko; Natalie V Dugger; Paul M Hoffman; Glen N Gaulton
Journal:  J Virol       Date:  2004-08       Impact factor: 5.103

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