| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 10931269 | 1093627 | 2016 | 16 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Multiple mouse models of primary lymphedema exhibit distinct defects in lymphovenous valve development
												
											ترجمه فارسی عنوان
													مدل های موش های چندگانه لنفدیم اولیه دارای نقایص متمایز در توسعه دریچه های لنفوژن هستند 
													
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																																												موضوعات مرتبط
												
													علوم زیستی و بیوفناوری
													بیوشیمی، ژنتیک و زیست شناسی مولکولی
													بیولوژی سلول
												
											چکیده انگلیسی
												Lymph is returned to the blood circulation exclusively via four lymphovenous valves (LVVs). Despite their vital importance, the architecture and development of LVVs is poorly understood. We analyzed the formation of LVVs at the molecular and ultrastructural levels during mouse embryogenesis and identified three critical steps. First, LVV-forming endothelial cells (LVV-ECs) differentiate from PROX1+ progenitors and delaminate from the luminal side of the veins. Second, LVV-ECs aggregate, align perpendicular to the direction of lymph flow and establish lympho-venous connections. Finally, LVVs mature with the recruitment of mural cells. LVV morphogenesis is disrupted in four different mouse models of primary lymphedema and the severity of LVV defects correlate with that of lymphedema. In summary, we have provided the first and the most comprehensive analysis of LVV development. Furthermore, our work suggests that aberrant LVVs contribute to lymphedema.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Developmental Biology - Volume 409, Issue 1, 1 January 2016, Pages 218-233
											Journal: Developmental Biology - Volume 409, Issue 1, 1 January 2016, Pages 218-233
نویسندگان
												Xin Geng, Boksik Cha, Md. Riaj Mahamud, Kim-Chew Lim, Robert Silasi-Mansat, Mohammad K.M. Uddin, Naoyuki Miura, Lijun Xia, Alexander M. Simon, James Douglas Engel, Hong Chen, Florea Lupu, R. Sathish Srinivasan, 
											