Intrinsic cardiac origin of human cardiosphere-derived cells

Cardiosphere-derived cells (CDCs) are in clinical development as a regenerative cell product which can be expanded ex vivo from patient cardiac biopsies. Cardiosphere-derived cells are clonogenic, exhibit multilineage differentiation, and exert functional benefits in preclinical models of heart fail...

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Veröffentlicht in:European heart journal 2013-01, Vol.34 (1), p.68-75
Hauptverfasser: White, Anthony J, Smith, Rachel R, Matsushita, Satoshi, Chakravarty, Tarun, Czer, Lawrence S C, Burton, Kevin, Schwarz, Ernst R, Davis, Darryl R, Wang, Qi, Reinsmoen, Nancy L, Forrester, James S, Marbán, Eduardo, Makkar, Raj
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container_issue 1
container_start_page 68
container_title European heart journal
container_volume 34
creator White, Anthony J
Smith, Rachel R
Matsushita, Satoshi
Chakravarty, Tarun
Czer, Lawrence S C
Burton, Kevin
Schwarz, Ernst R
Davis, Darryl R
Wang, Qi
Reinsmoen, Nancy L
Forrester, James S
Marbán, Eduardo
Makkar, Raj
description Cardiosphere-derived cells (CDCs) are in clinical development as a regenerative cell product which can be expanded ex vivo from patient cardiac biopsies. Cardiosphere-derived cells are clonogenic, exhibit multilineage differentiation, and exert functional benefits in preclinical models of heart failure. The origin of CDCs remains unclear: are these cells endogenous to the heart, or do they arise from cells that populate the heart via blood-borne seeding? Right ventricular endomyocardial biopsies were obtained from cardiac transplant recipients (n = 10, age 57 ± 15 years), and CDCs expanded from each biopsy. Donor-recipient mismatches were used to probe the origin of CDCs in three complementary ways. First, DNA analysis of short-tandem nucleotide repeats (STRs) was performed on genomic DNA from donor and recipient, then compared with the STR pattern of CDCs. Second, in two cases where the donor was male and the recipient female, CDCs were examined for the presence of X and Y chromosomes by fluorescence in situ hybridization. Finally, in two cases, quantitative PCR (qPCR) was performed for individual-specific polymorphisms of a major histocompatability locus to quantify the contribution of recipient cells to CDCs. In no case was recipient DNA detectable in the CDCs by STR analysis. In the two cases in which a female patient had received a male heart, all CDCs examined had an X and Y chromosome, similarly indicating exclusively donor origin. Likewise, qPCR on CDCs did not detect any recipient DNA. Cardiosphere-derived cells are of endogenous cardiac origin, with no detectable contribution from extra-cardiac seeding.
doi_str_mv 10.1093/eurheartj/ehr172
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Cardiosphere-derived cells are clonogenic, exhibit multilineage differentiation, and exert functional benefits in preclinical models of heart failure. The origin of CDCs remains unclear: are these cells endogenous to the heart, or do they arise from cells that populate the heart via blood-borne seeding? Right ventricular endomyocardial biopsies were obtained from cardiac transplant recipients (n = 10, age 57 ± 15 years), and CDCs expanded from each biopsy. Donor-recipient mismatches were used to probe the origin of CDCs in three complementary ways. First, DNA analysis of short-tandem nucleotide repeats (STRs) was performed on genomic DNA from donor and recipient, then compared with the STR pattern of CDCs. Second, in two cases where the donor was male and the recipient female, CDCs were examined for the presence of X and Y chromosomes by fluorescence in situ hybridization. Finally, in two cases, quantitative PCR (qPCR) was performed for individual-specific polymorphisms of a major histocompatability locus to quantify the contribution of recipient cells to CDCs. In no case was recipient DNA detectable in the CDCs by STR analysis. In the two cases in which a female patient had received a male heart, all CDCs examined had an X and Y chromosome, similarly indicating exclusively donor origin. Likewise, qPCR on CDCs did not detect any recipient DNA. 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source Oxford University Press Journals; MEDLINE; Free E-Journal (出版社公開部分のみ); Alma/SFX Local Collection
subjects Adult
Aged
Cell Differentiation - physiology
Cells, Cultured
DNA - analysis
Female
Heart Transplantation
Heart Ventricles - cytology
Humans
In Situ Hybridization, Fluorescence
Male
Microsatellite Repeats
Middle Aged
Myocardium - cytology
Myocytes, Cardiac - cytology
Real-Time Polymerase Chain Reaction
Stem Cell Transplantation - methods
Stem Cells - cytology
Young Adult
title Intrinsic cardiac origin of human cardiosphere-derived cells
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