| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 5506458 | 1400295 | 2017 | 37 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Programmed cell clearance: From nematodes to humans
												
											ترجمه فارسی عنوان
													از بین بردن سلول های برنامه ریزی شده: از نماتدها به انسان ها 
													
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																																												موضوعات مرتبط
												
													علوم زیستی و بیوفناوری
													بیوشیمی، ژنتیک و زیست شناسی مولکولی
													 زیست شیمی
												
											چکیده انگلیسی
												Programmed cell clearance is a highly regulated physiological process of elimination of dying cells that occurs rapidly and efficiently in healthy organisms. It thus ensures proper development as well as homeostasis. Recent studies have disclosed a considerable degree of conservation of cell clearance pathways between nematodes and higher organisms. The externalization of the anionic phospholipid phosphatidylserine (PS) has emerged as an important “eat-me” signal for phagocytes and its exposition on apoptotic cells is controlled by phospholipid translocases and scramblases. However, there is mounting evidence that PS exposure occurs not only in apoptosis, but may also be actively expressed on the surface of cells undergoing other forms of cell death including necrosis; PS is also expressed on the surface of engulfing cells. Additionally, PS may act as a “save-me” signal during axonal regeneration. Here we discuss mechanisms of PS exposure and its recognition by phagocytes as well as the consequences of PS signaling in nematodes and in mammals.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 482, Issue 3, 15 January 2017, Pages 491-497
											Journal: Biochemical and Biophysical Research Communications - Volume 482, Issue 3, 15 January 2017, Pages 491-497
نویسندگان
												Katharina Klöditz, Yu-Zen Chen, Ding Xue, Bengt Fadeel, 
											