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      Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment

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          Abstract

          Background

          Several studies have suggested that caffeic acid phenethyl ester (CAPE) can induce the expression of hypoxia inducible factor-1α (HIF-1α) protein. We determined whether CAPE has a novel function in improving the homing and engraftment of haematopoietic stem/progenitor cells (HSPCs) by regulating HIF-1α gene expression in the bone marrow (BM) niche.

          Methods

          For survival experiments, lethally irradiated C57BL/6 mice were injected with a low number of BM mononuclear cells (MNCs) and CAPE according to the indicated schedule. Homing efficiency analysis was conducted using flow cytometry and colony-forming unit (CFU) assays. The influence of intraperitoneal injection of CAPE on short-term and long-term engraftment of HSPCs was evaluated using competitive and non-competitive mouse transplantation models. To investigate the mechanism by which CAPE enhanced HSPC homing, we performed these experiments including Q-PCR, western blot, immunohistochemistry and CFU assays after in-vivo HIF-1α activity blockade.

          Results

          CAPE injection significantly increased the survival rate of recipient mice after lethal irradiation and transplantation of a low number of BM MNCs. Using HSPC homing assays, we found that CAPE notably increased donor HSPC homing to recipient BM. The subsequent short-term and long-term engraftment of transplanted HSPCs was also improved by the optimal schedule of CAPE administration. Mechanistically, we found that CAPE upregulated the expression of HIF-1α, vascular endothelial growth factor-A (VEGF-A) and stromal cell-derived factor 1α (SDF-1α). The HIF-1α inhibitor PX-478 blocked CAPE-enhanced HSPC homing, which supported the idea that HIF-1α is a key target of CAPE.

          Conclusions

          Our results showed that CAPE administration facilitated HSPC homing and engraftment, and this effect was primarily dependent on HIF-1α activation and upregulation of SDF-1α and VEGF-A expression in the BM niche.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s13287-017-0708-x) contains supplementary material, which is available to authorized users.

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          Most cited references36

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          Dependence of human stem cell engraftment and repopulation of NOD/SCID mice on CXCR4.

          Stem cell homing and repopulation are not well understood. The chemokine stromal cell-derived factor-1 (SDF-1) and its receptor CXCR4 were found to be critical for murine bone marrow engraftment by human severe combined immunodeficient (SCID) repopulating stem cells. Treatment of human cells with antibodies to CXCR4 prevented engraftment. In vitro CXCR4-dependent migration to SDF-1 of CD34+CD38-/low cells correlated with in vivo engraftment and stem cell function. Stem cell factor and interleukin-6 induced CXCR4 expression on CD34+ cells, which potentiated migration to SDF-1 and engraftment in primary and secondary transplanted mice. Thus, up-regulation of CXCR4 expression may be useful for improving engraftment of repopulating stem cells in clinical transplantation.
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            How do stem cells find their way home?

            Migration of hematopoietic stem cells through the blood, across the endothelial vasculature to different organs and to their bone marrow (BM) niches, requires active navigation, a process termed homing. Homing is a rapid process and is the first and essential step in clinical stem cell transplantation. Similarly, homing is required for seeding of the fetal BM by hematopoietic progenitors during development. Homing has physiological roles in adult BM homeostasis, which are amplified during stress-induced recruitment of leukocytes from the BM reservoir and during stem cell mobilization, as part of host defense and repair. Homing is thought to be a coordinated, multistep process, which involves signaling by stromal-derived factor 1 (SDF-1) and stem cell factor (SCF), activation of lymphocyte function-associated antigen 1 (LFA-1), very late antigen 4/5 (VLA-4/5) and CD44, cytoskeleton rearrangement, membrane type 1 (MT1)-matrix metalloproteinase (MMP) activation and secretion of MMP2/9. Rolling and firm adhesion of progenitors to endothelial cells in small marrow sinusoids under blood flow is followed by trans-endothelial migration across the physical endothelium/extracellular matrix (ECM) barrier. Stem cells finalize their homing uniquely, by selective access and anchorage to their specialized niches in the extravascular space of the endosteum region and in periarterial sites. This review is focused on mechanisms and key regulators of human stem cell homing to the BM in experimental animal models and clinical transplantation protocols.
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              Disruption of the CXCR4/CXCL12 chemotactic interaction during hematopoietic stem cell mobilization induced by GCSF or cyclophosphamide.

              Hematopoietic progenitor cells (HPCs) normally reside in the bone marrow (BM) but can be mobilized into the peripheral blood (PB) after treatment with GCSF or chemotherapy. In previous studies, we showed that granulocyte precursors accumulate in the BM during mobilization induced by either GCSF or cyclophosphamide (CY), leading to the accumulation of active neutrophil proteases in this tissue. We now report that mobilization of HPCs by GCSF coincides in vivo with the cleavage of the N-terminus of the chemokine receptor CXCR4 on HPCs resident in the BM and mobilized into the PB. This cleavage of CXCR4 on mobilized HPCs results in the loss of chemotaxis in response to the CXCR4 ligand, the chemokine stromal cell-derived factor-1 (SDF-1/CXCL12). Furthermore, the concentration of SDF-1 decreased in vivo in the BM of mobilized mice, and this decrease coincided with the accumulation of serine proteases able to directly cleave and inactivate SDF-1. Since both SDF-1 and its receptor, CXCR4, are essential for the homing and retention of HPCs in the BM, the proteolytic degradation of SDF-1, together with that of CXCR4, could represent a critical step leading to the mobilization of HPCs into the PB in response to GCSF or CY.
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                Author and article information

                Contributors
                chenxiaofang0209@163.com
                yemuhan@163.com
                bowen_0901@126.com
                liuym07@126.com
                wangsihan_lk@hotmail.com
                tutu52013@163.com
                ahmudzl@yeah.net
                fan17930@yeah.net
                static_1111@163.com
                hlj821@163.com
                wenyue226@126.com
                shirlylyh@126.com
                peixt@nic.bmi.ac.cn
                Journal
                Stem Cell Res Ther
                Stem Cell Res Ther
                Stem Cell Research & Therapy
                BioMed Central (London )
                1757-6512
                7 November 2017
                7 November 2017
                2017
                : 8
                : 255
                Affiliations
                [1 ]ISNI 0000 0000 8877 7471, GRID grid.284723.8, School of Laboratory Medicine and Biotechnology, , Southern Medical University, ; No. 1838 Guangzhou Avenue North, Baiyun District, Guangzhou, 510515 China
                [2 ]ISNI 0000 0004 0632 3409, GRID grid.410318.f, Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, ; No. 27 Taiping Road, Haidian District, Beijing, 100850 China
                [3 ]South China Institute of Biomedicine, No. 1 Luoxuan 4th Road, Haizhu District, Guangzhou, 510005 China
                [4 ]ISNI 0000 0004 1760 3078, GRID grid.410560.6, Guangdong Medical University, ; No. 1 Xincheng Road, Dongguan, 523808 China
                Author information
                http://orcid.org/0000-0001-8406-4762
                Article
                708
                10.1186/s13287-017-0708-x
                5678809
                29116023
                6d25af50-46df-4467-9ddd-8d88e6ecc1ca
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 25 April 2017
                : 24 August 2017
                : 23 October 2017
                Funding
                Funded by: National High Technology Research and Development Program of China
                Award ID: 2013AA020107
                Award Recipient :
                Funded by: Nature Science Foundation of China
                Award ID: 81472908
                Award Recipient :
                Funded by: Nature Science Foundation of China
                Award ID: 31401260
                Funded by: Guangzhou Health Care and Cooperative Innovation Major Project
                Award ID: 201400000003-4
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Molecular medicine
                caffeic acid phenethyl ester,haematopoietic stem/progenitor cells,homing,engraftment

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