Not just a marker: CD34 on human hematopoietic stem/progenitor cells dominates vascular selectin binding along with CD44

被引:87
作者
AbuSamra, Dina B. [1 ]
Aleisa, Fajr A. [1 ]
Al-Amoodi, Asma S. [1 ]
Ahmed, Heba M. Jalal [1 ]
Chin, Chee Jia [1 ]
Abuelela, Ayman F. [1 ]
Bergam, Ptissam [2 ]
Sougrat, Rachid [2 ]
Merzaban, Jasmeen S. [1 ]
机构
[1] King Abdullah Univ Sci & Technol, Div Biol & Environm Sci & Engn, Cell Migrat & Signaling Lab, Thuwal, Saudi Arabia
[2] King Abdullah Univ Sci & Technol, Imaging & Characterizat Core Facil, Thuwal, Saudi Arabia
关键词
ACUTE MYELOID-LEUKEMIA; P-SELECTIN; BONE-MARROW; STEM-CELLS; GLYCOPROTEIN LIGAND-1; PROGENITOR CELLS; ENDOTHELIAL SELECTINS; CORD-BLOOD; ADHESION MOLECULE-1; TYROSINE SULFATION;
D O I
10.1182/bloodadvances.2017004317
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
CD34 is routinely used to identify and isolate human hematopoietic stem/progenitor cells (HSPCs) for use clinically in bone marrow transplantation, but its function on these cells remains elusive. Glycoprotein ligands on HSPCs help guide their migration to specialized microvascular beds in the bone marrow that express vascular selectins (E- and P-selectin). Here, we show that HSPC-enriched fractions from human hematopoietic tissue expressing CD34 (CD34(pos)) bound selectins, whereas those lacking CD34 (CD34(neg)) did not. An unbiased proteomics screen identified potential glycoprotein ligands on CD34(pos) cells revealing CD34 itself as a major vascular selectin ligand. Biochemical and CD34 knockdown analyses highlight a key role for CD34 in the first prerequisite step of cell migration, suggesting that it is not just a marker on these cells. Our results also entice future potential strategies to investigate the glycoforms of CD34 that discriminate normal HSPCs from leukemic cells and to manipulate CD34(neg) HSPC-enriched bone marrow or cord blood populations as a source of stem cells for clinical use.
引用
收藏
页码:2799 / 2816
页数:18
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