Loss of Angiopoietin-like 7 diminishes the regeneration capacity of hematopoietic stem and progenitor cells

Springer Science and Business Media LLC - Tập 8 - Trang 1-5 - 2015
Yiren Xiao1,2, Xinru Wei1,2, Zhiwu Jiang1,2, Xiangmeng Wang3, Wei Ye1,2, Xin Liu4, Minjie Zhang4, Yan Xu5,6, Donghai Wu1,2, Liangxue Lai1,2, Huihui Yao7, Zixia Liu8, Su Cao9, Pentao Liu10, Bing Xu3, Yangqiu Li5,6, Yao Yao11, Duanqing Pei1,2, Peng Li1,2
1Key Laboratory of Regenerative Biology, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 7, China
2Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China
3Department of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China
4Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China
5Institute of Hematology, Medical College, Jinan University, Guangzhou, China
6Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University, Guangzhou, China
7Department of Outpatient, The 91th Military Hospital, Jiaozuo, China
8Division of Reproductive Endocrinology, The 91th Military Hospital, Jiaozuo, China
9Division of General Pediatrics, The 91th Military Hospital, Jiaozuo, China
10Wellcome Trust Sanger Institute, England, UK
11Drug Discovery Pipeline, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China

Tóm tắt

Successful expansion of hematopoietic stem cells (HSCs) would benefit the use of HSC transplants in the clinic. Angiopoietin-like 7 promotes the expansion of hematopoietic stem and progenitor cells (HSPC) in vitro and ex vivo. However, the impact of loss of Angptl7 on HSPCs in vivo has not been characterized. Here, we generated Angptl7-deficient mice by TALEN-mediated gene targeting and found that HSC compartments in Angptl7-null mice were compromised. In addition, wild type (WT) HSPCs failed to repopulate in the BM of Angptl7-null mice after serial transplantations while the engraftment of Angptl7-deficient HSPCs in WT mice was not impaired. These results suggest that Angptl7 is required for HSPCs repopulation in a non-cell autonomous manner.

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