Establishment of an in vitro cytotoxicity assay platform using primary monkey cardiomyocytes. (February 2019)
- Record Type:
- Journal Article
- Title:
- Establishment of an in vitro cytotoxicity assay platform using primary monkey cardiomyocytes. (February 2019)
- Main Title:
- Establishment of an in vitro cytotoxicity assay platform using primary monkey cardiomyocytes
- Authors:
- Iguchi, Takuma
Fujimoto, Kazunori
Nakamura, Shinichiro
Kishino, Hiroyuki
Niino, Noriyo
Mori, Kazuhiko - Abstract:
- Abstract: To establish an in vitro cytotoxicity assay platform using monkey cardiomyocytes, we isolated primary cardiomyocytes from fetal cynomolgus monkeys at different gestation days (from day 39 to 90) using the trypsin and collagenase digestion method, which was identical to the standard procedure for rat cardiomyocytes. Under these conditions, the primary cells obtained from monkeys at gestation day 63 or earlier showed spontaneous beating, with >80% cells being viable from all fetuses. Transcriptome analysis of the monkey cardiomyocytes indicated that the cells have essential components of cardiac functions, such as myosins, α-actin, cardiac troponins, and calcium-related molecules. The susceptibility to doxorubicin-induced cytotoxicity in monkey cardiomyocytes was comparable to that in rat cardiomyocytes, as evaluated based on intracellular ATP levels. Microarray analysis with Ingenuity Pathway Analysis revealed that doxorubicin predominantly increased the expression of several key genes involved in the endoplasmic reticulum stress pathway in monkey cardiomyocytes than in rat cardiomyocytes. In conclusion, we isolated primary monkey cardiomyocytes that showed similar sensitivity to doxorubicin as compared with rat cardiomyocytes. This in vitro monkey cardiomyocyte assay platform would serve as a powerful tool for the investigation of the interspecies differences in drug-induced cardiotoxicity and its underlying mechanism. Highlights: An in vitro cytotoxicity assayAbstract: To establish an in vitro cytotoxicity assay platform using monkey cardiomyocytes, we isolated primary cardiomyocytes from fetal cynomolgus monkeys at different gestation days (from day 39 to 90) using the trypsin and collagenase digestion method, which was identical to the standard procedure for rat cardiomyocytes. Under these conditions, the primary cells obtained from monkeys at gestation day 63 or earlier showed spontaneous beating, with >80% cells being viable from all fetuses. Transcriptome analysis of the monkey cardiomyocytes indicated that the cells have essential components of cardiac functions, such as myosins, α-actin, cardiac troponins, and calcium-related molecules. The susceptibility to doxorubicin-induced cytotoxicity in monkey cardiomyocytes was comparable to that in rat cardiomyocytes, as evaluated based on intracellular ATP levels. Microarray analysis with Ingenuity Pathway Analysis revealed that doxorubicin predominantly increased the expression of several key genes involved in the endoplasmic reticulum stress pathway in monkey cardiomyocytes than in rat cardiomyocytes. In conclusion, we isolated primary monkey cardiomyocytes that showed similar sensitivity to doxorubicin as compared with rat cardiomyocytes. This in vitro monkey cardiomyocyte assay platform would serve as a powerful tool for the investigation of the interspecies differences in drug-induced cardiotoxicity and its underlying mechanism. Highlights: An in vitro cytotoxicity assay using fetal monkey cardiomyocytes was established. The cytotoxicity towards doxorubicin was comparable between monkey and rat. Doxorubicin increased endoplasmic reticulum stress pathway in monkey cardiomyocytes. … (more)
- Is Part Of:
- Toxicology in vitro. Volume 54(2019)
- Journal:
- Toxicology in vitro
- Issue:
- Volume 54(2019)
- Issue Display:
- Volume 54, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 54
- Issue:
- 2019
- Issue Sort Value:
- 2019-0054-2019-0000
- Page Start:
- 130
- Page End:
- 136
- Publication Date:
- 2019-02
- Subjects:
- Cardiomyocyte -- Cynomolgus monkey -- In vitro cytotoxicity -- Microarray -- Doxorubicin -- Endoplasmic reticulum stress
IPA Ingenuity Pathway Analysis -- GO Gene Ontology -- hiPSC-CM human pluripotent stem cell-derived cardiomyocyte -- ER endoplasmic reticulum
Toxicity testing -- In vitro -- Periodicals
Toxicology -- Periodicals
615.9 - Journal URLs:
- http://www.sciencedirect.com/science/journal/08872333 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.tiv.2018.09.012 ↗
- Languages:
- English
- ISSNs:
- 0887-2333
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8873.043400
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8849.xml