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Wharton's jelly or bone marrow mesenchymal stromal cells improve cardiac function following myocardial infarction for more than 32 weeks in a rat model: a preliminary report.在大鼠模型中,Wharton 胶或骨髓间充质基质细胞在心肌梗死后 32 周以上可改善心功能:初步报告。
Curr Stem Cell Res Ther. 2013 Jan;8(1):46-59. doi: 10.2174/1574888x11308010007.
2
E2F4 is required for cardiomyocyte proliferation.E2F4 对于心肌细胞增殖是必需的。
Cardiovasc Res. 2010 Apr 1;86(1):92-102. doi: 10.1093/cvr/cvp383. Epub 2009 Dec 2.
3
TWEAK is a positive regulator of cardiomyocyte proliferation.TWEAK 是心肌细胞增殖的正向调节因子。
Cardiovasc Res. 2010 Mar 1;85(4):681-90. doi: 10.1093/cvr/cvp360. Epub 2009 Nov 2.
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Evidence for cardiomyocyte renewal in humans.人类心肌细胞更新的证据。
Science. 2009 Apr 3;324(5923):98-102. doi: 10.1126/science.1164680.
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Advances in specific immunotherapy for prostate cancer.前列腺癌特异性免疫疗法的进展。
Eur Urol. 2008 Apr;53(4):694-708. doi: 10.1016/j.eururo.2007.11.043. Epub 2007 Nov 26.
6
Evidence from a genetic fate-mapping study that stem cells refresh adult mammalian cardiomyocytes after injury.一项基因命运图谱研究的证据表明,干细胞在损伤后可更新成年哺乳动物的心肌细胞。
Nat Med. 2007 Aug;13(8):970-4. doi: 10.1038/nm1618. Epub 2007 Jul 29.
7
Periostin induces proliferation of differentiated cardiomyocytes and promotes cardiac repair.骨膜蛋白可诱导分化的心肌细胞增殖并促进心脏修复。
Nat Med. 2007 Aug;13(8):962-9. doi: 10.1038/nm1619. Epub 2007 Jul 15.
8
Therapeutic delivery of cyclin A2 induces myocardial regeneration and enhances cardiac function in ischemic heart failure.细胞周期蛋白A2的治疗性递送可诱导心肌再生并增强缺血性心力衰竭中的心脏功能。
Circulation. 2006 Jul 4;114(1 Suppl):I206-13. doi: 10.1161/CIRCULATIONAHA.105.000455.
9
Adenoviral gene transfer of FGF-5 to hibernating myocardium improves function and stimulates myocytes to hypertrophy and reenter the cell cycle.将FGF-5通过腺病毒基因转移至冬眠心肌可改善其功能,并刺激心肌细胞肥大并重新进入细胞周期。
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10
Postnatal isl1+ cardioblasts enter fully differentiated cardiomyocyte lineages.出生后的Isl1+成心细胞进入完全分化的心肌细胞谱系。
Nature. 2005 Feb 10;433(7026):647-53. doi: 10.1038/nature03215.

急性心肌梗死诱导功能性心肌细胞重新进入细胞周期。

Acute myocardial infarction induced functional cardiomyocytes to re-enter the cell cycle.

机构信息

Department of Cardiology, Zhongda Hospital, Medical School of Southeast University Nanjing, China.

出版信息

Am J Transl Res. 2013 Apr 19;5(3):327-35. Print 2013.

PMID:23634243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3633975/
Abstract

BACKGROUND

Loss of cardiomyocytes after myocardial infarction (MI) causes heart failure. In this study, we investigate whether the in situ cardiomyocytes can re-enter the cell cycle and to what extent cell division of cardiomyocytes occurs after acute MI (AMI) in rats.

METHODS

Sprague Dawley (SD) rats were used in this study; the left anterior descending coronary artery was ligated. At time points (3 days, 1 week, 2 weeks, 3 weeks, and 4 weeks) after the operation, five rats were euthanized, respectively. An additional five sham-operated rats serves as a control group and were euthanized at 3 days post-operation. The expressions of cyclin A2, Ki-67, phospho-histone H3 (H3P), and Aurora B in myocardial tissues were detected by Western blot and immunofluorescence.

RESULTS

The expression levels of cyclin A2 were significantly higher in all groups with AMI except the 4-week group than those found in the sham-operated group (P < 0.01). The percentage of Ki-67-positive nuclei in the border zones was significantly higher than the percentage in the distant normal myocardium (P < 0.01).

CONCLUSIONS

our results demonstrate that cardiomyocytes re-enter the cell cycle after AMI and that cyclin A2 is a reliable marker for the detection of cell cycle activity in cardiomyocytes.

摘要

背景

心肌梗死后心肌细胞的丢失会导致心力衰竭。在这项研究中,我们研究了在大鼠急性心肌梗死(AMI)后,原位心肌细胞是否可以重新进入细胞周期,以及心肌细胞分裂的程度。

方法

本研究使用 Sprague Dawley(SD)大鼠;结扎左前降支冠状动脉。手术后的时间点(3 天、1 周、2 周、3 周和 4 周),分别处死 5 只大鼠。另外 5 只假手术大鼠作为对照组,在手术后 3 天处死。通过 Western blot 和免疫荧光检测心肌组织中细胞周期蛋白 A2、Ki-67、磷酸化组蛋白 H3(H3P)和 Aurora B 的表达。

结果

除 4 周组外,所有 AMI 组的 cyclin A2 表达水平均明显高于假手术组(P < 0.01)。边缘区 Ki-67 阳性核的百分比明显高于远侧正常心肌的百分比(P < 0.01)。

结论

我们的结果表明,AMI 后心肌细胞重新进入细胞周期,细胞周期蛋白 A2 是检测心肌细胞周期活性的可靠标志物。