Nip21 gene expression reduces coxsackievirus B3 replication by promoting apoptotic cell death via a mitochondria-dependent pathway

Huifang M. Zhang, Bobby Yanagawa, Paul Cheung, Honglin Luo, Ji Yuan, David Chau, Aikun Wang, Lubos Bohunek, Janet E. Wilson, Bruce M. McManus, Decheng Yang

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

Our previous studies, using differential mRNA display, suggested that the mouse Nip21 gene may be involved in myocarditis development in the coxsackievirus B3 (CVB3)-infected mouse heart. Sequence comparison indicated that the mouse Nip21 gene shares high sequence homology to human Nip2. This human protein is known to interact with both the apoptosis inhibitor Bcl-2 and a homologous protein, the adenovirus E1B 19-kDa protein. Such interactions implicate Nip21 gene in cell death pathways. To study the function of this gene, we have cloned Nip21 from mouse hearts and established a Tet-On doxycycline-inducible HeLa cell line and a cardiomyocyte H9c2 cell line expressing Nip21 to characterize gene function in relation to apoptosis. We demonstrated that Nip21 expression could induce apoptosis via caspase-depended mitochondria activation. To further determine the function of Nip21 in CVB3-induced apoptosis, the Tet-On/Nip21 HeLa cell line was induced by doxycycline followed by CVB3 infection. We found that activation of caspase-3 and cleavage of poly-(ADP-ribose) polymerase occurred 2 hours earlier than in vector-transfected control cells, suggesting that Nip21 expression enhances CVB3-induced apoptosis. We also demonstrated a significant decrease in HeLa cell and H9c2 cell viability. Particularly, as illustrated by viral plaque assay, CVB3 replication was dramatically reduced in Tet-On HeLa cells, due at least in part to the earlier killing of the host cells by Nip21 overexpression.

Original languageEnglish (US)
Pages (from-to)1251-1258
Number of pages8
JournalCirculation Research
Volume90
Issue number12
DOIs
StatePublished - Jun 28 2002

Fingerprint

Enterovirus
Mitochondria
Cell Death
HeLa Cells
Apoptosis
Gene Expression
Doxycycline
Genes
Cell Line
Adenovirus E1B Proteins
Viral Plaque Assay
Coxsackievirus Infections
Poly(ADP-ribose) Polymerases
Myocarditis
Gene Expression Profiling
Sequence Homology
Caspases
Cardiac Myocytes
Caspase 3
Cell Survival

Keywords

  • Apoptosis
  • Coxsackievirus B3
  • Myocarditis
  • Nip21

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Nip21 gene expression reduces coxsackievirus B3 replication by promoting apoptotic cell death via a mitochondria-dependent pathway. / Zhang, Huifang M.; Yanagawa, Bobby; Cheung, Paul; Luo, Honglin; Yuan, Ji; Chau, David; Wang, Aikun; Bohunek, Lubos; Wilson, Janet E.; McManus, Bruce M.; Yang, Decheng.

In: Circulation Research, Vol. 90, No. 12, 28.06.2002, p. 1251-1258.

Research output: Contribution to journalArticle

Zhang, HM, Yanagawa, B, Cheung, P, Luo, H, Yuan, J, Chau, D, Wang, A, Bohunek, L, Wilson, JE, McManus, BM & Yang, D 2002, 'Nip21 gene expression reduces coxsackievirus B3 replication by promoting apoptotic cell death via a mitochondria-dependent pathway', Circulation Research, vol. 90, no. 12, pp. 1251-1258. https://doi.org/10.1161/01.RES.0000024690.69379.5C
Zhang, Huifang M. ; Yanagawa, Bobby ; Cheung, Paul ; Luo, Honglin ; Yuan, Ji ; Chau, David ; Wang, Aikun ; Bohunek, Lubos ; Wilson, Janet E. ; McManus, Bruce M. ; Yang, Decheng. / Nip21 gene expression reduces coxsackievirus B3 replication by promoting apoptotic cell death via a mitochondria-dependent pathway. In: Circulation Research. 2002 ; Vol. 90, No. 12. pp. 1251-1258.
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AU - Chau, David

AU - Wang, Aikun

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