Proteomic Profiling of Secreted Proteins for the Hematopoietic Support of Interleukin-Stimulated Human Umbilical Vein Endothelial Cells

被引:6
作者
Bal, Guerkan [1 ]
Kamhieh-Milz, Julian [1 ]
Sterzer, Viktor [1 ]
Al-Samman, Muhammad [1 ]
Debski, Janusz [2 ]
Kein, Oliver [3 ]
Kamhieh-Milz, Sundrela [1 ]
Bhakdi, Sucharit [4 ]
Salama, Abdulgabar [1 ]
机构
[1] Charite, Inst Transfus Med, D-13353 Berlin, Germany
[2] Polish Acad Sci, Inst Biochem & Biophys, Warsaw, Poland
[3] Charite, Berlin Brandenburg Ctr Regenerat Therapies, D-13353 Berlin, Germany
[4] Johannes Gutenberg Univ Mainz, Inst Med Microbiol & Hyg, D-55122 Mainz, Germany
关键词
Endothelial cells (ECs); Hematopoietic stem and progenitor cells (HSPCs); Expansion; Proteomics; Interleukin stimulated; C5B-9 COMPLEMENT COMPLEX; EX-VIVO EXPANSION; CORD BLOOD-CELLS; PROGENITOR CELLS; SELF-RENEWAL; STEM-CELLS; TNF-ALPHA; STEM/PROGENITOR CELLS; GENE-TRANSFER; KAPPA-B;
D O I
10.3727/096368912X657288
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human umbilical cord vein endothelial cells (HUVECs) secrete a number of factors that greatly impact the proliferation and differentiation of hematopoietic stem and progenitor cells (HSPCs). These factors remain largely unknown. Here, we report on the most comprehensive proteomic profiling of the HUVEC secretome and identified 827 different secreted proteins. Two hundred and thirty-one proteins were found in all conditions, whereas 369 proteins were identified only under proinflammatory conditions following IL-1 beta, IL-3, and IL-6 stimulation. Thirteen proteins including complement factor b (CFb) were identified only under IL-1 beta and IL-3 conditions and may potentially represent HSPC proliferation factors. The combination of bioinformatics and gene ontology annotations indicates the role of the complement system and its activation. Furthermore, CFb was found to be transcriptionally strongly upregulated. Addition of complement component 5b-9 (C5b-9) monoclonal antibody to the stem cell expansion assay was capable of significantly reducing their proliferation. This study suggests a complement-mediated cross-talk between endothelial cells and HSPCs under proinflammatory conditions.
引用
收藏
页码:1185 / 1199
页数:15
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