Inhibition of SRC-mediated integrin signaling in bone marrow niche enhances hematopoietic stem cell function

抑制骨髓微环境中SRC介导的整合素信号传导可增强造血干细胞功能。

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作者:Irene Mariam Roy,P V Anu,Samantha Zaunz,Srinu Reddi,Aravind M Giri,Rithika Saroj Sankar,Sarah Schouteden,Joerg Huelsken,Catherine M Verfaillie,Satish Khurana

Abstract

Interaction with microenvironmental factors is crucial for the regulation of hematopoietic stem cell (HSC) function. Stroma derived factor (SDF)-1α supports HSCs in the quiescent state and is central to the homing of transplanted HSCs. Here, we show that integrin signaling regulates Sdf-1α expression transcriptionally. Systemic deletion of Periostin, an Integrin-αv ligand, showed increased expression of Sdf-1α in bone marrow (BM) niche. Pharmacological inhibition or CRISPR-Cas9-mediated deletion of SRC, resulted in a similar increase in the chemokine expression in vitro. Importantly, systemic SRC-inhibition led to increase in SDF-1α levels in BM plasma. This resulted in a robust increase (14.05 ± 1.22% to 29.11 ± 0.69%) in the homing efficiency of transplanted HSCs. In addition, we observed enhancement in the recovery of blood cell counts following radiation injury, indicating an enhanced hematopoietic function. These results establish a role of SRC-mediated integrin signaling in the transcriptional regulation of Sdf-1α. This mechanism could be harnessed further to improve the hematopoietic function.

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