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January 1, 1997AJP Heart and Circulatory Physiology304 citations

Assessment of cardiomyocyte DNA synthesis in normal and injured adult mouse hearts

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MSMark H. SoonpaaIndiana University School of MedicineLFLoren J. FieldUniversity of North Carolina at Chapel Hill

Key Result

Focal cauterization injury in adult mouse hearts resulted in extremely rare cardiomyocyte DNA synthesis, with only 3 synthetic nuclei per 36,000 cells compared to a 0.0005% index in normal hearts.

Key Points

  • This research aims to assess cardiomyocyte DNA synthesis in both normal and injured adult mouse hearts.
  • Cardiomyocyte DNA synthesis was monitored using [3H]thymidine incorporation and autoradiographic analysis.
  • A high throughput assay developed utilized transgenic mice expressing a nuclear-localized beta-galactosidase reporter gene.
  • Examinations involved 20,000 normal ventricular cardiomyocytes and 36,000 nuclei in the perinecrotic zone of injured hearts.
  • In normal hearts, a maximum labeling index of 0.0005% was observed with a single synthetic nucleus identified among 180,000 examined.
  • Only three synthetic nuclei were found in 36,000 nuclei from the injured heart's perinecrotic zone, and none in 180,000 nuclei from distal regions.

Structured PICO

P
Population
Normal and injured adult mouse hearts, including transgenic mice expressing a nuclear-localized beta-galactosidase (beta-Gal) reporter gene exclusively in cardiac myocytes.
I
Intervention
Myocardial injury induced by focal cauterization of the left ventricular free wall
C
Comparator
Normal adult mouse hearts (uninjured)
O
Outcome
Cardiomyocyte DNA synthesis (labeling index) measured by [3H]thymidine incorporation and autoradiographic analysissurrogate

Cardiomyocyte DNA synthesis in both normal and injured adult mouse hearts is extremely rare, establishing a baseline for evaluating regenerative capacity in genetically modified models.

Main Result

Absolute Event Rate: 0.0083% vs 0.0005%

Abstract

Cardiomyocyte DNA synthesis was examined in normal and injured adult mouse hearts. In preliminary studied DNA synthesis was monitored by 3Hthymidine incorporation, followed by autoradiographic analysis of dispersed cell preparations. No synthetic cells were identified when 20,000 ventricular cardiomyocytes from normal adult hearts were examined. A high throughput assay was developed to establish the actual labeling index for the adult mouse heart. The assay utilized 3Hthymidine incorporation in transgenic mice which expressed a nuclear-localized beta-galactosidase (beta-Gal) reporter gene exclusively in cardiac myocytes. Cardiomyocyte DNA synthesis was evidenced by colocalization of beta-Gal activity and silver grains in autoradiograms of histological sections. Examination of 180,000 ventricular cardiomyocyte nuclei from normal adult transgenic mice identified a single synthetic nucleus, suggesting a maximum labeling index of 0.0005%. Cardiomyocyte DNA synthesis was next examined in hearts injured by focal cauterization of the left ventricular free wall. Only three synthetic nuclei were identified when 36,000 cardiomyocyte nuclei in the perinecrotic zone of the injured heart were examined. No additional synthetic nuclei were identified when 180,000 nuclei in regions distal to the necrotic zone were examined. These data confirm that cardiomyocyte DNA synthesis in the adult mouse heart is extremely rare and provide baseline data for analyses in genetically modified animals.

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Cite This Study

Soonpaa et al. (1997) studied Myocardial injury (mouse model). Focal cauterization of the left ventricular free wall vs. Normal adult mouse hearts was evaluated on Cardiomyocyte DNA synthesis (labeling index). Focal cauterization injury in adult mouse hearts resulted in extremely rare cardiomyocyte DNA synthesis, with only 3 synthetic nuclei per 36,000 cells compared to a 0.0005% index in normal hearts.

synapsesocial.com/papers/6a0ba9b34f6759c6fca2561fhttps://doi.org/10.1152/ajpheart.1997.272.1.h220
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