| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 8472100 | 1550292 | 2018 | 8 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Hepatic leukemia-associated macrophages exhibit a pro-inflammatory phenotype in Notch1-induced acute T cell leukemia
												
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																																												کلمات کلیدی
												iNOSTAMsM1 polarizationHCC - HCCT-ALL - بلند قدSpleen - طحالT cell acute lymphoblastic leukemia - لوسمی لنفوبلاستی حاد T-سلولیTumor-associated macrophages - ماکروفاژهای مربوط به تومورbone marrow - مغز استخوانHepatomegaly - هپاتومگالیHepatocellular carcinoma - کارسینوم هپاتوسلولار(کارسینوم سلولهای استخوانی)
												موضوعات مرتبط
												
													علوم زیستی و بیوفناوری
													بیوشیمی، ژنتیک و زیست شناسی مولکولی
													بیولوژی سلول
												
											پیش نمایش صفحه اول مقاله
												 
												چکیده انگلیسی
												Tumor-associated macrophages (TAMs) are well accepted and the pathological role of macrophages in hematopoietic malignancies have been proposed. Hepatomegaly is frequently observed in T cell acute lymphoblastic leukemia (T-ALL) patients with poor prognosis. However, the role of leukemia-associated macrophages (LAMs) in hepatic microenvironment remains unclear. Here, the characteristics of hepatic LAMs (H-LAMs) were studied in Notch1 induced T-ALL model. Increase in proportion and absolute counts of H-LAMs was detected with infiltration of inflammatory cells. Furthermore, H-LAMs exhibited a more M1-like phenotype distinct from that of TAMs in hepatocellular carcinoma and LAMs from BM or spleen in leukemia. Moreover, H-LAMs expressed increased level of cytokines in charge of recruiting inflammatory cells, which contributed to pro-inflammatory hepatic microenvironment.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Immunobiology - Volume 223, Issue 1, January 2018, Pages 73-80
											Journal: Immunobiology - Volume 223, Issue 1, January 2018, Pages 73-80
نویسندگان
												Xiao Yang, Wenli Feng, Rong Wang, Feifei Yang, Lina Wang, Shayan Chen, Chong Chen, Qian Ren, Guoguang Zheng,