Regulatory T Cells Dynamically Regulate Selectin Ligand Function during Multiple Challenge Contact Hypersensitivity

作者: Latasha D. Abeynaike , James A. Deane , Clare L. V. Westhorpe , Zachary Chow , Maliha A. Alikhan

DOI: 10.4049/JIMMUNOL.1400641

关键词:

摘要: Regulatory T cells (Tregs) play critical roles in restricting cell-mediated inflammation. In the skin, this is dependent on expression of selectin ligands required for leukocyte rolling dermal microvessels. However, whether there are differences molecules used by Tregs and proinflammatory to undergo skin remains unclear. study, we spinning disk confocal microscopy Foxp3-GFP mice visualize endogenous postcapillary venules. underwent consistent but low-frequency interactions under resting inflamed conditions. At early stage response, Treg adhesion was minimal. at peak inflammation, made up 40% adherent CD4(+) cell population. a multiple challenge model contact hypersensitivity, conventional mostly overlapping contributions P- E-selectin. after second challenge, not became P-selectin independent, showed reduced capacity bind P-selectin. Moreover, inhibition E-selectin time point resulted exacerbation These findings demonstrate that binding molecular basis can be regulated dynamically.

参考文章(61)
Issekutz Tb, Dual inhibition of VLA-4 and LFA-1 maximally inhibits cutaneous delayed-type hypersensitivity-induced inflammation. American Journal of Pathology. ,vol. 143, pp. 1286- 1293 ,(1993)
M Ursula Norman, Karyn J Lister, Yuan H Yang, Andrew Issekutz, Michael J Hickey, TNF regulates leukocyte–endothelial cell interactions and microvascular dysfunction during immune complex-mediated inflammation British Journal of Pharmacology. ,vol. 144, pp. 265- 274 ,(2005) , 10.1038/SJ.BJP.0706081
M. Ursula Norman, Sara Hulliger, Pina Colarusso, Paul Kubes, Multichannel fluorescence spinning disk microscopy reveals early endogenous CD4 T cell recruitment in contact sensitivity via complement. Journal of Immunology. ,vol. 180, pp. 510- 521 ,(2008) , 10.4049/JIMMUNOL.180.1.510
Kubes P, Kanwar S, McCafferty Dm, Hickey Mj, Eppihimer Mj, Granger Dn, Varying Roles of E-Selectin and P-Selectin in Different Microvascular Beds in Response to Antigen Journal of Immunology. ,vol. 162, pp. 1137- 1143 ,(1999)
Kelly L. Davenpeck, Mary E. Brummet, Sherry A. Hudson, Ruth J. Mayer, Bruce S. Bochner, Activation of human leukocytes reduces surface P-selectin glycoprotein ligand-1 (PSGL-1, CD162) and adhesion to P-selectin in vitro. Journal of Immunology. ,vol. 165, pp. 2764- 2772 ,(2000) , 10.4049/JIMMUNOL.165.5.2764
R E Tigelaar, B L Gocinski, Roles of CD4+ and CD8+ T cells in murine contact sensitivity revealed by in vivo monoclonal antibody depletion. Journal of Immunology. ,vol. 144, pp. 4121- 4128 ,(1990)
R.P. McEver, K.L. Moore, D.E. Lyons, R.D. Cummings, S.F. Eaton, H.S. Lichenstein, The P-selectin glycoprotein ligand from human neutrophils displays sialylated, fucosylated, O-linked poly-N-acetyllactosamine. Journal of Biological Chemistry. ,vol. 269, pp. 23318- 23327 ,(1994) , 10.1016/S0021-9258(17)31656-3
Ada M. Kruisbeek, Ethan Shevach, Angela M. Thornton, Proliferative assays for T cell function. Current protocols in immunology. ,vol. 60, ,(2004) , 10.1002/0471142735.IM0312S60