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Th1-Like ICOS+ Foxp3+ Treg Cells Preferentially Express CXCR3 and Home to β-Islets during Pre-Diabetes in BDC2.5 NOD Mice

Fig 1

Autoreactive T cell-mediated inflammation induces CXCR3 expression by ICOS+ Treg cells prior to T1D onset.

Cell suspensions of pancreas and draining LN from 4 week old (A, B) WT and (B) ICOS-/- BDC2.5 mice were assessed for the frequency of CXCR3+ cells and levels of CXCR3 expression (MFI) between the ICOS+ and ICOS- subsets of Treg cells. (C and D) NOD.TCRα-/- mice received MACS sorted BDC2.5 CD4+CD25+ (Treg, 0.75X105) or CD4+CD25- (Teff, 7.5X105) cells alone or at the indicated Treg/Teff cell ratios. When the Teff cell recipient mice displayed hyperglycemia (>33mmol/L), mice were sacrificed and expression of IFN-γ by Teff cells (C) and CXCR3+ percent cells among the ICOS+ Treg cell subset were assessed. (E) NOD.TCRα-/- mice received the indicated ratios of FACS-sorted Thy1.2+ Treg cells to 7.5X105 BDC2.5 Thy1.1+ CD4+Foxp3- Teff cells. After 14 days, the Thy1.2 (tTreg) and Thy1.1+ (pTreg) subsets of ICOS+ Treg cells were compared for percent CXCR3+ cells. (n = 4, peri LN = pooled axial, brachial and inguinal peripheral lymph nodes).

Fig 1

doi: https://doi.org/10.1371/journal.pone.0126311.g001