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Vanessa Brochard, Béhazine Combadière, Annick Prigent, Yasmina Laouar, Aline Perrin, Virginie Beray-Berthat, Olivia Bonduelle, Daniel Alvarez-Fischer, Jacques Callebert, Jean-Marie Launay, Charles Duyckaerts, Richard A. Flavell, Etienne C. Hirsch, Stéphane Hunot
Published in Volume 119, Issue 1
J Clin Invest. 2009; 119(1):182–192 doi:10.1172/JCI36470
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Figure 4
Mice deficient in CD4+ T cells are more resistant to MPTP.

(A) Quantification of TH+ DNs in the SNpc at day 7 after MPTP (4 × 18 mg/kg) or saline treatment in WT, Tcrb–/–, Cd8a–/–, and Cd4–/– mice. Bars represent the mean number of total nigral TH+ DNs. Open symbols indicate saline-treated animals and filled symbols indicate MPTP-treated animals. Each symbol represents 1 individual animal. A significant protection against MPTP-induced DN cell loss is observed in Tcrb–/– and Cd4–/– mice but not in Cd8a–/– animals as compared with their WT littermates. *P < 0.05 compared with MPTP-treated WT and Cd8a–/– mice; P = 0.956 compared with MPTP-treated WT littermates (Tukey post-hoc analysis). Nissl+ cell counts confirmed that TH+ cell loss was not a consequence of downregulated expression of TH (data not shown). (B) Representative photomicrographs of mesencephalic sections immunostained for TH with Nissl counterstain from saline- or MPTP-treated WT and lymphocytic deficient mice. Insets show Mac-1+ microglial cells (arrows) in the SNpc from the same animals. Scale bar: 300 μm; 100 μm (insets). (C) Quantification of the total number of infiltrated CD4+ and CD8+ T cells in the SNpc from MPTP-treated WT and lymphocytic deficient mice. MPTP-treated Cd8a–/– mice display as many CD4+ T cells as MPTP-treated WT littermates. **P < 0.05 compared with saline-injected WT mice (Mann-Whitney U test). ††P < 0.001 compared with MPTP-treated WT and Cd8a–/– mice; #P < 0.001 compared with MPTP-treated WT mice (Dunn test). ND, not detected.