Cadaveric cardiosphere-derived cells can maintain regenerative capacity and improve the heart function of cardiomyopathy. Issue 9 (2nd May 2016)
- Record Type:
- Journal Article
- Title:
- Cadaveric cardiosphere-derived cells can maintain regenerative capacity and improve the heart function of cardiomyopathy. Issue 9 (2nd May 2016)
- Main Title:
- Cadaveric cardiosphere-derived cells can maintain regenerative capacity and improve the heart function of cardiomyopathy
- Authors:
- Sun, Yong
Chi, Di
Tan, Miaoxin
Kang, Kai
Zhang, Maomao
Jin, Xiangyuan
Leng, Xiaoping
Cao, Rui
Liu, Xianglan
Yu, Bo
Wu, Jian - Abstract:
- ABSTRACT: Objective : Cardiosphere-derived cells (CDCs) improve cardiac function and attenuate remodeling in ischemic and non-ischemic cardiomyopathy, and are currently obtained through myocardial biopsy. However, there is not any study on whether functional CDCs may be obtained through cadaveric autopsy with similar benefits in non-ischemic cardiomyopathy.Methods : Cardiac tissues from human or mouse cadavers were harvested, plated at 4°C, and removed at varying time points to culture human CDCs (CLH-EDCs) and mouse CDCs (CM-CDCs). The differentiation and paracrine effects of CDCs were also assessed. Furthermore, intramyocardial injection of cadaveric CM-CDCs was performed in an induced dilated cardiomyopathy (DCM) model.Results : With the extension of post mortem hours, the number of CLH-EDCs and CM-CDCs harvested from autopsy specimens decreased. The expressions of von Willebrand factor (VWF) and smooth muscle actin (SMA) on CDCs were gradually reduced, however, cardiac troponin I (TNI) expression increased in the 24 h group compared to the 0 h group. CLH-EDCs were also found to have similar paracrine function in the 24 h group compared to 0 h group. 8 weeks after CM-CDCs transplantion to the injured heart, mean left ventricular ejection fraction increased in both 0 h (64.99 ± 3.4%) and 24 h (62.99 ± 2.8%) CM-CDCs-treated groups as compared to the PBS treated group (53.64 ± 5.6 cm), with a decrease in left ventricular internal diastolic diameter (0.29 ± 0.08 cm and 0.32 ±ABSTRACT: Objective : Cardiosphere-derived cells (CDCs) improve cardiac function and attenuate remodeling in ischemic and non-ischemic cardiomyopathy, and are currently obtained through myocardial biopsy. However, there is not any study on whether functional CDCs may be obtained through cadaveric autopsy with similar benefits in non-ischemic cardiomyopathy.Methods : Cardiac tissues from human or mouse cadavers were harvested, plated at 4°C, and removed at varying time points to culture human CDCs (CLH-EDCs) and mouse CDCs (CM-CDCs). The differentiation and paracrine effects of CDCs were also assessed. Furthermore, intramyocardial injection of cadaveric CM-CDCs was performed in an induced dilated cardiomyopathy (DCM) model.Results : With the extension of post mortem hours, the number of CLH-EDCs and CM-CDCs harvested from autopsy specimens decreased. The expressions of von Willebrand factor (VWF) and smooth muscle actin (SMA) on CDCs were gradually reduced, however, cardiac troponin I (TNI) expression increased in the 24 h group compared to the 0 h group. CLH-EDCs were also found to have similar paracrine function in the 24 h group compared to 0 h group. 8 weeks after CM-CDCs transplantion to the injured heart, mean left ventricular ejection fraction increased in both 0 h (64.99 ± 3.4%) and 24 h (62.99 ± 2.8%) CM-CDCs-treated groups as compared to the PBS treated group (53.64 ± 5.6 cm), with a decrease in left ventricular internal diastolic diameter (0.29 ± 0.08 cm and 0.32 ± 0.04 cm in 0 h and 24 h groups, vs. 0.41 ± 0.05 cm in PBS group).Conclusion : CDCs from cadaveric autopsy are highly proliferative and differentiative, and may be used as a source for allograft transplantation, in order to decrease myocardial fibrosis, attenuate left ventricular remodeling, and improve heart function in doxorubicin-induced non-ischemic cardiomyopathy. … (more)
- Is Part Of:
- Cell cycle. Volume 15:Issue 9(2016)
- Journal:
- Cell cycle
- Issue:
- Volume 15:Issue 9(2016)
- Issue Display:
- Volume 15, Issue 9 (2016)
- Year:
- 2016
- Volume:
- 15
- Issue:
- 9
- Issue Sort Value:
- 2016-0015-0009-0000
- Page Start:
- 1248
- Page End:
- 1256
- Publication Date:
- 2016-05-02
- Subjects:
- allograft transplantation -- cadaver -- cardiosphere-derived cells -- dilated cardiomyopathy
Cell cycle -- Periodicals
571.84377 - Journal URLs:
- http://www.tandfonline.com/ ↗
http://www.tandfonline.com/toc/kccy20/current ↗ - DOI:
- 10.1080/15384101.2016.1160973 ↗
- Languages:
- English
- ISSNs:
- 1538-4101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.746500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1141.xml