کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2820011 1569943 2006 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Macrophage MHC receptor 2: A novel receptor on allograft (H-2DdKd)-induced macrophage (H-2DbKb) recognizing an MHC class I molecule, H-2Kd, in mice
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی ژنتیک
پیش نمایش صفحه اول مقاله
Macrophage MHC receptor 2: A novel receptor on allograft (H-2DdKd)-induced macrophage (H-2DbKb) recognizing an MHC class I molecule, H-2Kd, in mice
چکیده انگلیسی

We previously reported that a population of allograft (H-2DdKd)-induced macrophages (AIM) in C57BL/6 (H-2DbKb) mice exhibited major histocompatibility complex (MHC) haplotype (H-2Dd) specific killing of the allograft (e.g., BALB/c skin and Meth A cells; H-2DdKd) in a macrophage MHC receptor (MMR)-dependent manner. In the present study, we isolated a cDNA clone encoding a novel receptor (MMR2) on AIM recognizing another MHC class I molecule, H-2Kd, by the expression cloning method using H-2Kd tetramer and a monoclonal antibody (mAb; R12) specific for AIM. The cDNA (2359-bp) encoded a 677-amino acid polypeptide of a calculated molecular mass of 87 kDa and was found to be expressed exclusively on AIM among cells infiltrating into allografts on days 0–9 after transplantation. Confocal microscopy showed that HEK293T cells transfected with this cDNA were reactive toward the H-2Kd molecule but not toward other MHC class I molecules such as H-2Dd, H-2Db, H-2Dk, H-2Kb, H-2Kk, and H-2Ld molecules. The binding of the H-2Kd molecule to the transfectants was inhibited by the addition of R12 or anti-H-2Kd, but not by R15 (a mAb specific for H-2Dd receptor) or anti-H-2Dd, mAb. Flow cytometric analysis revealed specific binding of H-2Kd molecules to AIM (Kd = 2.7 × 10− 9 M); and the binding was completely suppressed by the addition of R12 mAb. These results demonstrate that a novel receptor (MMR2) for H-2Kd molecules was induced on effector macrophages responsible for allograft (H-2DdKd) rejection by H-2DbKb mice.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 384, 15 December 2006, Pages 1–8
نویسندگان
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