Journal of Molecular Engineering & Systems Biology

Journal of Molecular Engineering & Systems Biology

ISSN 2050-1412
Original Research

The expression of scavenger receptor B2 in enterovirus 71-infected mice

Ji-an Li and Zong-bo Chen*

*Correspondence: Zong-bo Chen

Author Affiliations

Pediatric Department of the Affiliated Hospital of Qingdao University Medical School, NO.16 Jiangsu, Road, Qingdao 266003, PR China.


Objectives: Scavenger receptor class B, member 2 (SCARB2) participates in early innate immune responses to infection, so our aim was to explore the expression and role of mouse SCARB2 (mSCARB2) in different tissues in EV71-infected mice.

Methods: ICR mice were inoculated intraperitoneally (i.p.) with EV71 0.1 ml 107.5 TCID50/ml. The control mice were injected i.p. with the same volume RD cell lysate. Mice were sacrificed by aether anesthesia at day 4, 8 and 12 post infection (p.i.), their brain, brainstem, spinal cord, cerebellum, lung and heart were dissected out for determining the number of copies of viral RNA by quantitative real-time PCR (qRT-PCR), detection of expression of mSCARB2 by immunohistochemistry, qRT-PCR and Westernblotting. Cytokines quantification by ELISA.

Results: The viral loads in central nervous system (CNS) were higher than in lung or/and heart. The expression of mSCARB2 increased in tissues of EV71-infected mice, however, the levels of mSCARB2 increased in CNS were higher than in lung or/and heart within a certain period of time, particularly in brainstem and brain. In addition, local TNF-α, IL-6 and IL-1β levels of production were consistent with mSCARB2 levels of expression in tissues of EV71-infected mice. However, it presented a positive correlation between relative mSCARB2 mRNA level and TNF-α, IL-6 and IL-1β levels in local tissues at day 4 and 8 p.i.

Conclusions: Our data revealed that the elevated local mSCARB2 may modulate pro-inflammatory cytokines induction in local tissues, particularly, in CNS of EV71-infected mice.

Keywords: Enterovirus 71, mice, mSCARB2, pro-inflammatory cytokines

ISSN 2050-1412
Volume 3
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