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Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment
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 re...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678809/ https://www.ncbi.nlm.nih.gov/pubmed/29116023 http://dx.doi.org/10.1186/s13287-017-0708-x |
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author | Chen, Xiaofang Han, Yi Zhang, Bowen Liu, Yiming Wang, Sihan Liao, Tuling Deng, Ziliang Fan, Zeng Zhang, Jing He, Lijuan Yue, Wen Li, Yanhua Pei, Xuetao |
author_facet | Chen, Xiaofang Han, Yi Zhang, Bowen Liu, Yiming Wang, Sihan Liao, Tuling Deng, Ziliang Fan, Zeng Zhang, Jing He, Lijuan Yue, Wen Li, Yanhua Pei, Xuetao |
author_sort | Chen, Xiaofang |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5678809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56788092017-11-17 Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment Chen, Xiaofang Han, Yi Zhang, Bowen Liu, Yiming Wang, Sihan Liao, Tuling Deng, Ziliang Fan, Zeng Zhang, Jing He, Lijuan Yue, Wen Li, Yanhua Pei, Xuetao Stem Cell Res Ther Research 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. BioMed Central 2017-11-07 /pmc/articles/PMC5678809/ /pubmed/29116023 http://dx.doi.org/10.1186/s13287-017-0708-x Text en © 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. |
spellingShingle | Research Chen, Xiaofang Han, Yi Zhang, Bowen Liu, Yiming Wang, Sihan Liao, Tuling Deng, Ziliang Fan, Zeng Zhang, Jing He, Lijuan Yue, Wen Li, Yanhua Pei, Xuetao Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment |
title | Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment |
title_full | Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment |
title_fullStr | Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment |
title_full_unstemmed | Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment |
title_short | Caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment |
title_sort | caffeic acid phenethyl ester promotes haematopoietic stem/progenitor cell homing and engraftment |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678809/ https://www.ncbi.nlm.nih.gov/pubmed/29116023 http://dx.doi.org/10.1186/s13287-017-0708-x |
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