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Identification of functional endothelial progenitor cells suitable for the treatment of ischemic tissue using human umbilical cord blood Authors: Source: Blood, July 2007. Outlines 1. Background : a. Endothelial progenitor cell ( EPC ) b. Aldehyde dehydrogenase activity ( ALDH ) 2. Experimental design & Results a. Isolation of EPC b. Characterization of EPC c. Function assays In vivo & In vitro 3. Conclusion Endothelial progenitor cells ( EPC ) ◆ originally identified from human peripheral blood ( PB ) ◆ also isolated from bone marrow , fetal liver, and umbilical cord blood. Endothelial progenitor cells ( EPC ) ◆ Physiologic functions: ◆ Therapeutic angiogenesis : Limb ischemia Myocardial infarction The definition of an EPC The definition of an EPC ◆ Hur et al. ( Arteriosclerosis Thrombosis , and Vascular Biology.2004 ) Source Early EPC Late EPC Adult peripheral blood mononuclear cells Exponential growth Surface marker 2 to 3 weeks CD45,CD14 4 to 8 weeks CD31,CD34,VEGFR2 , and VEcadherin ◆ Ingram et al.( Blood,2004) ● divided subpopulations according to clonogenic and proliferative potential. ● Highly & Low proliferative endothelial potential-colony-forming cells ( HPP-ECFCs & LPP- ECFCs ) ◆ Yoder et al ( Blood,2007 ) ● Progeny of CD45+CD14+ cells are not EPCs but hematopoietic-derived myeloid progenitor cells. Aldehyde dehydrogenase ( ALDH ) ◆ Functions: ● Oxidized intercellular aldehyde and involved in ethanol, vitamin A , and cyclophosphamide metabolism. ● High levels in hematopoietic progenitor and stem cells ( HPC & HSC ). ● The higher ALDH activity HSC expressed, the better progenitor function and repopulation activity worked. ◆ Detection: ● Fluorescent aldehyde substrate (Dansyl aminoacetaldehyde, Aldefluor ) by flow cytometry. Aim: To develop an appropriate procedure for isolating EPCs from UCB to improve therapeutic efficacy and eliminate the expansion of nonessential cells. Isolation of EPCs Step 1 Isolation of UCB-derived EPCs by negative immunoselection Red blood cell surface marker: glycophorin A Isolation of UCB-derived EPCs by negative immunoselection UCB Hematopoietic cell surface markers: CD3, CD14, CD19, CD38, CD66b. Red blood cell marker: glycophorin A Characterization of EPCs by uptake of Dil-Ac-LDL Cell morphology Bright field Cobblestone-like clusters Dark field PE-conjugated Dil-Ac-LDL marker: a. Dil-acetylated low-density lipoprotein b. Uptake of Dil-Ac-LDL by endothelial cells & macrophages as scavengers. Characterization of EPCs by flow cytometry sorting Step 2 CD45- / Ac-LDL+ CD31+ / Ac-LDL+ CD45: Hematopoietic stem cell surface marker Ac-LDL+/CD31+/CD45- cells EC-like morphology Analysis of endothelial tube formation of EPCs in Matrigel Matrigel : A. Solubilized basement membrane matrix . B. Rich in extracellular matrix proteins. C. Endothelial cells formed capillary tube in matrigel. Ac-LDL+/CD31+/CD45- cells Capillary tube-like structure on Matrigel Conclusion Characterization of isolated EPCs Endothelial cell morphology Ac-LDL+/CD31+/CD45- cells Capillary tube formation in matrigel Separation of EPCs according to the ALDH activity Aldefluor : ALDH substrate Alde-High EPC Alde-Low EPC Characterization of Alde-High & Alde-Low EPCs Endothelial cell–specific cell surface markers Characterization of Alde-High & Alde-Low EPCs Hematopoietic stem cell surface markers Conclusion EPCs can divide two groups according to ALDH activity. Alde-High & Alde-Low EPCs : EC-specific markers No hematopoietic stem cells Growth rate of Alde-High & Alde-Low EPCs under hypoxia In Vitro Growth rate Capillary formation of Alde-High & Alde-Low EPCs under hypoxia In Vitro Capillary networks formation in Matrigel The assay of migration activity of EPCs by transwell culture in Vitro Transwell culture system EPCs SDF-1 SDF-1 : Homing factor The assay of migration activity of EPCs under hypoxia in Vitro The Hypoxia inducible pathway Analyses of gene expression in EPCs under hypoxia In Vitro VEGF: Vascular endothelial growth factor KDR : VEGF receptor 2 Flt-1: VEGF receptor 1 CXCR4: SDF-1 receptor Glut-1: Glucose transporter-1 The Hypoxia inducible pathway Protein expression in HIF-1α & 2α under hypoxia In Vitro Conclusion Under hypoxia Alde-High EPCs V.S. Alde-Low EPCs Growth rate Lower Faster Tube numbers formation More Less Migration cell numbers Less More Hypoxia-inducible gene & protein expression Less More The functional assay for neovascularization of EPCs in vivo A murine stem cell virus (MSCV)–internal ribosomal entry site–enhanced GFP Flap ischemia mice model Tail vein 7 days Ischemia recovery 2X3 cm EPCs The effect of EPCs in neovascularization in vivo Tracking the Alde-Low EPCs location in the ischemia tissue Neovascularization TRITC-Lectin: glycoprotein binding protein Newly formed vessels Tracking the Alde-Low EPCs location in the ischemia tissue Re-endothelialization Dorsal ischemia skin Conclusion A novel method for isolating EPCs from UCB by a combination of negative immunoselection and cell culture techniques. ALDH activity may serve as an excellent marker for isolating EPCs from UCB for clinical cell therapy. Alde-Low EPCs possess a greater ability to proliferate and migrate compared to those with Alde-High EPCs . Introduction of Alde-Low EPCs may be a potential strategy for inducing rapid neovascularization and regeneration of ischemic tissues.