4.3 Article

Vasoactive intestinal peptide receptor 1 is downregulated during expansion of antigen-specific CD8 T cells following primary and secondary Listeria monocytogenes infections

Journal

JOURNAL OF NEUROIMMUNOLOGY
Volume 234, Issue 1-2, Pages 40-48

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jneuroim.2011.02.002

Keywords

Neuropeptide; Neuropeptide receptor; Memory T cells; CD8 T cell; VIP; VPAC1

Funding

  1. National Institutes of Health (NIH) [K01 DK064828]
  2. National Institutes of Diabetes, Digestive and Kidney Diseases (NIDDK)
  3. National Center of Research Resources (NCRR) [P20 RR015566-07]

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As regulation of CD8 T cell homeostasis is incompletely understood, we investigated the expression profile of the vasoactive intestinal peptide (VIP) receptors, VPAC1 and VPAC2, on CD8 T cells throughout an in vivo immune response. Herein, we show that adoptively transferred CD8 T cells responding to a Listeria monocytogenes infection significantly downregulated, functionally active VPAC1 protein expression during primary and secondary expansion. VPAC1 mRNA expression was restored during contraction and regained naive levels in primary, but remained low during secondary, memory generation. VIP co-administration with primary infection suppressed CD8 T cell expansion (approximate to 50%). VPAC2 was not detected at any time points throughout primary and secondary infections. Collectively, our data demonstrate that functionally active VPAC1 is dynamically downregulated to render expanding CD8 T cells unresponsive to VIP. (C) 2011 Elsevier B.V. All rights reserved.

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