Genetic Lineage Tracing of Nonmyocyte Population by Dual Recombinases. Issue 8 (21st August 2018)
- Record Type:
- Journal Article
- Title:
- Genetic Lineage Tracing of Nonmyocyte Population by Dual Recombinases. Issue 8 (21st August 2018)
- Main Title:
- Genetic Lineage Tracing of Nonmyocyte Population by Dual Recombinases
- Authors:
- Li, Yan
He, Lingjuan
Huang, Xiuzhen
Bhaloo, Shirin Issa
Zhao, Huan
Zhang, Shaohua
Pu, Wenjuan
Tian, Xueying
Li, Yi
Liu, Qiaozhen
Yu, Wei
Zhang, Libo
Liu, Xiuxiu
Liu, Kuo
Tang, Juan
Zhang, Hui
Cai, Dongqing
Ralf, Adams H.
Xu, Qingbo
Lui, Kathy O.
Zhou, Bin - Abstract:
- Abstract : Background: Whether the adult mammalian heart harbors cardiac stem cells for regeneration of cardiomyocytes is an important yet contentious topic in the field of cardiovascular regeneration. The putative myocyte stem cell populations recognized without specific cell markers, such as the cardiosphere-derived cells, or with markers such as Sca1 +, Bmi1 +, Isl1 +, or Abcg2 + cardiac stem cells have been reported. Moreover, it remains unclear whether putative cardiac stem cells with unknown or unidentified markers exist and give rise to de novo cardiomyocytes in the adult heart. Methods: To address this question without relying on a particular stem cell marker, we developed a new genetic lineage tracing system to label all nonmyocyte populations that contain putative cardiac stem cells. Using dual lineage tracing system, we assessed whether nonmyocytes generated any new myocytes during embryonic development, during adult homeostasis, and after myocardial infarction. Skeletal muscle was also examined after injury for internal control of new myocyte generation from nonmyocytes. Results: By this stem cell marker–free and dual recombinases–mediated cell tracking approach, our fate mapping data show that new myocytes arise from nonmyocytes in the embryonic heart, but not in the adult heart during homeostasis or after myocardial infarction. As positive control, our lineage tracing system detected new myocytes derived from nonmyocytes in the skeletal muscle after injury.Abstract : Background: Whether the adult mammalian heart harbors cardiac stem cells for regeneration of cardiomyocytes is an important yet contentious topic in the field of cardiovascular regeneration. The putative myocyte stem cell populations recognized without specific cell markers, such as the cardiosphere-derived cells, or with markers such as Sca1 +, Bmi1 +, Isl1 +, or Abcg2 + cardiac stem cells have been reported. Moreover, it remains unclear whether putative cardiac stem cells with unknown or unidentified markers exist and give rise to de novo cardiomyocytes in the adult heart. Methods: To address this question without relying on a particular stem cell marker, we developed a new genetic lineage tracing system to label all nonmyocyte populations that contain putative cardiac stem cells. Using dual lineage tracing system, we assessed whether nonmyocytes generated any new myocytes during embryonic development, during adult homeostasis, and after myocardial infarction. Skeletal muscle was also examined after injury for internal control of new myocyte generation from nonmyocytes. Results: By this stem cell marker–free and dual recombinases–mediated cell tracking approach, our fate mapping data show that new myocytes arise from nonmyocytes in the embryonic heart, but not in the adult heart during homeostasis or after myocardial infarction. As positive control, our lineage tracing system detected new myocytes derived from nonmyocytes in the skeletal muscle after injury. Conclusions: This study provides in vivo genetic evidence for nonmyocyte to myocyte conversion in embryonic but not adult heart, arguing again the myogenic potential of putative stem cell populations for cardiac regeneration in the adult stage. This study also provides a new genetic strategy to identify endogenous stem cells, if any, in other organ systems for tissue repair and regeneration. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Circulation. Volume 138:Issue 8(2018)
- Journal:
- Circulation
- Issue:
- Volume 138:Issue 8(2018)
- Issue Display:
- Volume 138, Issue 8 (2018)
- Year:
- 2018
- Volume:
- 138
- Issue:
- 8
- Issue Sort Value:
- 2018-0138-0008-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-08-21
- Subjects:
- cell lineage -- myocardial infarction -- myocardial revascularization -- myocytes, cardiac -- recombinases -- stem cell
Blood -- Circulation -- Periodicals
Cardiovascular system -- Periodicals
Cardiology -- Periodicals
Heart -- Diseases -- Periodicals
Blood Circulation
Cardiovascular System
Vascular Diseases
616.1 - Journal URLs:
- http://ovidsp.tx.ovid.com/sp-3.4.2a/ovidweb.cgi?&S=HFFJFPCLPODDKOLGNCALDCMCIACKAA00&Browse=Toc+Children%7cNO%7cS.sh.1384_1326796138_84.1384_1326796138_96.1384_1326796138_97%7c66%7c50 ↗
http://www.circulationaha.org ↗
http://circ.ahajournals.org/ ↗
http://journals.lww.com ↗ - DOI:
- 10.1161/CIRCULATIONAHA.118.034250 ↗
- Languages:
- English
- ISSNs:
- 0009-7322
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3265.200000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7388.xml