Expression and age-related changes of centromere A in rat heart

FENG Ying YIN Guo-tian LI Ai-rong GUO Zhi-kun

Acta Anatomica Sinica ›› 2018, Vol. 49 ›› Issue (4) : 512-517.

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Acta Anatomica Sinica ›› 2018, Vol. 49 ›› Issue (4) : 512-517. DOI: 10.16098/j.issn.0529-1356.2018.04.016
Histology,Embryology and Developmental Biology

Expression and age-related changes of centromere A in rat heart

  • FENG Ying YIN Guo-tian LI Ai-rong* GUO Zhi-kun*
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Abstract

Objective  To study the expression and age-related changes of centromere protein A(CENP-A) in the rat heart. Methods  Ten rats in each group were collected from postnatal 1 day, 1 week old, 2 weeks old, 3 weeks old, 4 weeks old, 3 months old, 6 months old. The expression and age-related changes of CENP-A in the rat heart were observed by the immunohistochemistry, immunofluorescence, Western blotting, and Real-time PCR techniques. The CENP-A proteins of seven groups were quantitated by SPSS 20.0 statistical software. Results  CENP-A was mainly expressed in the vascular wall, epicardium and epicardial tissue and in a very few cardiomyocytes. The CENP-A in vascular wall was of stable expression with age. But the expression of CENP-A in the epicardium and subepicardial tissues was gradually reduced, which showed that postnatal 1 day was the most and 6 months old are the least. CENP-A in the vascular wall was mainly expressed in the smooth muscle cells, and was basically unchanged with ages.A small number of cardiac myocytes near the subepicardium also express CENP-A, and decreased with age. Conclusion  The expression of CENP-A in the rat heart gradually decreased with aging, but in the vascular wall remained stable expression.

Key words

Centromere protein-A / Myocardial tissue / Epicardium / Heart / Immunohistochemistry / Immunofluorescence / Rat

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FENG Ying YIN Guo-tian LI Ai-rong GUO Zhi-kun. Expression and age-related changes of centromere A in rat heart[J]. Acta Anatomica Sinica. 2018, 49(4): 512-517 https://doi.org/10.16098/j.issn.0529-1356.2018.04.016

References

[1] Liang QJ. Centromeric and kinetochore [J]. Bulletin of Biology,2012,47(4):1-4.(in Chinese)
 梁前进.着丝粒和动粒[J].生物学通报,2012,47(4):1-4.
[2] Li YM,Zhu MH.Advances in biological functions of centromere protein A [J]. Chinese Journal of Pathology,2006,35(12):750-751.  (in Chinese)
 李咏梅,朱明华.着丝粒蛋白A的生物学功能研究进展[J].中华病理学杂志,2006,35(12):750-751.
[3] Athwal RK, Walkiewicz MP, Baek S, et al. CENP-A nucleosomes localize to transcription factor hotspots and subtelomeric sites in human cancer cells[J].Epigenetics Chromatin, 2015, 8(1):2.
[4] Zhang W, Mao JH, Zhu W, et al. Centromere and kinetochore gene misexpression predicts cancer patient survival and response to radiotherapy and chemotherapy[J].Nat Commun, 2016,7:12619.
[5] Li YM,Liu XH, Cao XZh,et al. Expression of centromere protein A in primary hepatocellular carcinoma [J]. Chinese Journal of Pathology,2007,36(3):175-178.  (in Chinese)
李咏梅,刘晓红,曹晓哲,等.着丝粒蛋白A在原发性肝癌中的表达[J].中华病理学杂志,2007,36(3):175-178.
[6] Li Y, Zhu Z, Zhang S, et al. ShRNA-targeted centromere protein A inhibits hepatocellular carcinoma growth[J]. PLoS One, 2011,6(3):e17794.
[7] Maehara K, Takahashi K. CENP-A reduction induces a p53-dependent cellular senescence response to protect cells from executing defective mitoses[J]. Mol Cell Biol, 2010, 3(9):2090-2104.
[8] McGregor M, Hariharan N, Joyo AY, et al. CENP-A is essential for cardiac progenitor cell proliferation[J]. Cell Cycle, 2014, 13(5):739-748.
[9] Howman EV, Fowler KJ, Newson AJ, et al. Early disruption of centromeric chromatin organization in centromere protein A (Cenpa) null mice[J]. Proc Natl Acad Sci USA, 2000,97(3):1148-1153.
[10] Park KC, Lee M, Jeon Y, et al. Skin-specific deletion of mis18α impedes proliferation and stratification of epidermal keratinocytes[J]. Invest Dermator, 2017,137(2):414-421.
[11] Chen JJ, Zhao Q. Myocardial regeneration——from parenchyma to interstitial [J]. International Journal of Cardiovascular Disease, 2013,40(5):285-287. (in Chinese)
陈俊佶, 赵强. 心肌再生——从实质到间质[J]. 国际心血管病杂志, 2013,40(5):285-287.
[12] Bergmann O, Bhardwaj RD, Bernard S. Evidence for cardiomyocyte renewal in humans[J]. Science, 2009,324(5923):98-102.
[13] Han C, Nie Y, Lian H, et al. Acute inflammation stimulates a regenerative response in the neonatal mouse heart[J]. Cell Res, 2015,25(10):1137-1151.
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