Fas deficiency leads to decreased spontaneous apoptosis and accumulation of lymphocytes and myeloid cells in vivo in mice. (A) Phenotype of Faslpr mice. Shown are lymph nodes of WT and of Faslpr mice. The arrows point to the lymph nodes. Ruler in mm scale. (B-E) Spleens were collected from WT (n = 3) and Faslpr (n = 3) mice. Cells were stained with Annexin V and PI and analyzed by flow cytometry. PI+ cells were gated (B) and quantified as total cell death (C). Annexin V+ and PI+ cells were gated (D) and quantified for apoptotic cell death (E). (F) Thymuses, LNs, and spleens were collected from WT (n = 3) and Faslpr (n = 3) mice. Cells were stained with the indicated cell surface marker–specific antibodies and analyzed by flow cytometry.
Figure 2.

Fas deficiency leads to decreased spontaneous apoptosis and accumulation of lymphocytes and myeloid cells in vivo in mice. (A) Phenotype of Faslpr mice. Shown are lymph nodes of WT and of Faslpr mice. The arrows point to the lymph nodes. Ruler in mm scale. (B-E) Spleens were collected from WT (n = 3) and Faslpr (n = 3) mice. Cells were stained with Annexin V and PI and analyzed by flow cytometry. PI+ cells were gated (B) and quantified as total cell death (C). Annexin V+ and PI+ cells were gated (D) and quantified for apoptotic cell death (E). (F) Thymuses, LNs, and spleens were collected from WT (n = 3) and Faslpr (n = 3) mice. Cells were stained with the indicated cell surface marker–specific antibodies and analyzed by flow cytometry.

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