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Expression of M-Sec in CD3+CD4+CADM1+ cells.

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posted on 2021-11-29, 19:00 authored by Masateru Hiyoshi, Naofumi Takahashi, Youssef M. Eltalkhawy, Osamu Noyori, Sameh Lotfi, Jutatip Panaampon, Seiji Okada, Yuetsu Tanaka, Takaharu Ueno, Jun-ichi Fujisawa, Yuko Sato, Tadaki Suzuki, Hideki Hasegawa, Masahito Tokunaga, Yorifumi Satou, Jun-ichirou Yasunaga, Masao Matsuoka, Atae Utsunomiya, Shinya Suzu

(A) The CD3+CD4+CADM1+ cells in the live cell gate were sorted from PBMCs of HTLV-1 carriers. The profile of an HTLV-1 carrier is shown as an example. (B) The CD3+CD4+CADM1+ cells sorted from PBMCs of an HTLV-1 carrier were cultured for 3 days, and analyzed for M-Sec (green) and CD3 (red). The nuclei were also stained with DAPI (blue). Monocytes were added as a positive control for M-Sec. The antibodies used for staining were as follows: anti-M-Sec (F-6; Santa Cruz Biotechnology), and anti-CD3 (CD3-12; Abcam). Scale bar: 10 μm. (C) The cells were analyzed as in (B), and the percentages of CD3+CD4+CADM1+ cells or monocytes expressing M-Sec at a detectable level are shown (15 cells for each). The typical signal of monocytes was defined as “bright”.

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