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红细胞衍生的微泡可能会将磷脂酰丝氨酸转移到有核细胞表面,并错误地将它们“标记”为凋亡细胞。

Erythrocyte-derived microvesicles may transfer phosphatidylserine to the surface of nucleated cells and falsely 'mark' them as apoptotic.

作者信息

Liu Rui, Klich Izabela, Ratajczak Janina, Ratajczak Mariusz Z, Zuba-Surma Ewa K

机构信息

Stem Cell Institute at James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.

出版信息

Eur J Haematol. 2009 Sep;83(3):220-9. doi: 10.1111/j.1600-0609.2009.01271.x. Epub 2009 Apr 24.

Abstract

Lysis of erythrocytes using hypotonic solutions is one approach to remove red blood cells (RBCs) from umbilical cord blood (UCB), bone marrow (BM), and peripheral blood (PB) before flow cytometric analysis or sorting of nucleated cells (NCs). Our team employed this separation step to prepare UCB-, BM-, or PB-derived cells to sort very small embryonic-like stem cells (VSELs). We noticed that depletion of RBCs from UCB by hypotonic lysis resulted in a significant increase in the number of NCs including VSELs that bind Annexin-V (Ann-V). Surprisingly, these cells were not apoptotic and displayed normal proliferative potential. To explain this discrepancy, we show that RBC-derived microvesicles (RMV) released during erythrocyte lysis may transfer phosphatidylserine (PS) to the surface of NCs and 'mark' them falsely positive as apoptotic cells. This observation should be considered whenever Ann-V binding viability assays are employed to evaluate the quality of NCs depleted from erythrocytes via hypotonic lysis.

摘要

使用低渗溶液裂解红细胞是在对有核细胞(NCs)进行流式细胞术分析或分选之前,从脐带血(UCB)、骨髓(BM)和外周血(PB)中去除红细胞(RBCs)的一种方法。我们的团队采用这一分离步骤来制备源自UCB、BM或PB的细胞,以分选非常小的胚胎样干细胞(VSELs)。我们注意到,通过低渗裂解从UCB中去除RBCs会导致包括与膜联蛋白-V(Ann-V)结合的VSELs在内的NCs数量显著增加。令人惊讶的是,这些细胞并非凋亡细胞,且具有正常的增殖潜力。为了解释这一差异,我们发现红细胞裂解过程中释放的红细胞衍生微泡(RMV)可能会将磷脂酰丝氨酸(PS)转移到NCs表面,并将它们误标记为凋亡细胞。每当采用Ann-V结合活力测定法来评估通过低渗裂解从红细胞中去除的NCs的质量时,都应考虑这一观察结果。

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