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含地中海贫血症DNA的红细胞处于氧化应激状态。

Thalassemic DNA-Containing Red Blood Cells Are under Oxidative Stress.

作者信息

Dana Mutaz, Prus Eugenia, Fibach Eitan

机构信息

Department of Hematology, Hadassah-Hebrew University Medical Center, Ein-Kerem, P.O. Box 12000, Jerusalem 91120, Israel.

出版信息

Anemia. 2012;2012:943974. doi: 10.1155/2012/943974. Epub 2012 Mar 4.

Abstract

We studied the nature of enucleated RBCs containing DNA remnants, Howell-Jolly (HJ) RBCs and reticulocytes (retics), that are characteristically present in the circulation of thalassemic patients, especially after splenectomy. Using flow cytometry methodology, we measured oxidative status parameters of these cells in patients with β-thalassemia. In each patient studied, these cells had higher content of reactive oxygen species and exposed phosphatidylserine compared with their DNA-free counterparts. These results suggest that oxidative stress in thalassemic developing erythroid precursors might, through DNA-breakage, generate HJ-retics and HJ-RBCs and that oxidative stress-induced externalization of phosphatidylserine is involved in the removal of these cells from the circulation by the spleen, a mechanism similar to that of the removal of senescent RBCs.

摘要

我们研究了含有DNA残余物的去核红细胞、豪-乔(HJ)红细胞和网织红细胞(网织细胞)的性质,这些细胞在β地中海贫血患者的循环系统中具有特征性存在,尤其是在脾切除术后。我们使用流式细胞术方法,测量了β地中海贫血患者这些细胞的氧化状态参数。在每个研究对象中,与无DNA的对应细胞相比,这些细胞具有更高的活性氧含量和暴露的磷脂酰丝氨酸。这些结果表明,地中海贫血发育中的红系前体细胞中的氧化应激可能通过DNA断裂产生HJ-网织细胞和HJ-红细胞,并且氧化应激诱导的磷脂酰丝氨酸外化参与了脾脏将这些细胞从循环中清除的过程,这一机制类似于衰老红细胞的清除机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0afb/3310241/1295480b751f/ANE2012-943974.001.jpg

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