کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
922074 1473914 2016 16 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Immature monocytes recruited to the ischemic mouse brain differentiate into macrophages with features of alternative activation
ترجمه فارسی عنوان
مونوسیت ها خام وناقص استخدام به مغز موش های ایسکمیک به ماکروفاژها افتراق با ویژگی های فعال سازی جایگزین
کلمات کلیدی
ایسکمی مغزی؛ مونوسیت ها؛ ماکروفاژها؛ میکروگلیا؛ فنوتیپ جایگزین M2
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
چکیده انگلیسی


• Ly6ChiCD43lo cells are the predominant monocytes infiltrating the ischemic tissue.
• Monocytes reach the infarcted core along blood vessels from the leptomeninges.
• Monocytes lose their typical blood features and differentiate to macrophages.
• Infiltrated monocytes acquire features of alternatively activated macrophages.

Acute stroke induces a local inflammatory reaction causing leukocyte infiltration. Circulating monocytes are recruited to the ischemic brain and become tissue macrophages morphologically indistinguishable from reactive microglia. However, monocytes are a heterogeneous population of cells with different functions. Herein, we investigated the infiltration and fate of the monocyte subsets in a mouse model of focal brain ischemia by permanent occlusion of the distal portion of the middle cerebral artery. We separated two main subtypes of CD11bhi monocytes according to their expression of the surface markers Ly6C and CD43. Using adoptive transfer of reporter monocytes and monocyte depletion, we identified the pro-inflammatory Ly6ChiCD43loCCR2+ subset as the predominant monocytes recruited to the ischemic tissue. Monocytes were seen in the leptomeninges from where they entered the cortex along the penetrating arterioles. Four days post-ischemia, they had invaded the infarcted core, where they were often located adjacent to blood vessels. At this time, Iba-1− and Iba-1+ cells in the ischemic tissue incorporated BrdU, but BrdU incorporation was rare in the reporter monocytes. The monocyte phenotype progressively changed by down-regulating Ly6C, up-regulating F4/80, expressing low or intermediate levels of Iba-1, and developing macrophage morphology. Moreover, monocytes progressively acquired the expression of typical markers of alternatively activated macrophages, like arginase-1 and YM-1. Collectively, the results show that stroke mobilized immature pro-inflammatory Ly6ChiCD43lo monocytes that acutely infiltrated the ischemic tissue reaching the core of the lesion. Monocytes differentiated to macrophages with features of alternative activation suggesting possible roles in tissue repair during the sub-acute phase of stroke.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain, Behavior, and Immunity - Volume 53, March 2016, Pages 18–33
نویسندگان
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