Gene expression and cellular changes in injured myocardium of Ciona intestinalis

被引:0
作者
Stokes, Serenity [1 ]
Palmer, Pooja Pardhanani [2 ]
Barth, Jeremy L. [3 ]
Price, Robert L. [4 ]
Parker, Bella G. [5 ]
Anderson, Heather J. Evans [6 ]
机构
[1] Cent Piedmont Community Coll, Nat Sci Div, Charlotte, NC USA
[2] Atrium Hlth, Div Community & Social Impact, Charlotte, NC USA
[3] Med Univ South Carolina, Dept Regenerat Med & Cell Biol, MUSC Proteogen Facil, Charleston, SC 29425 USA
[4] Univ South Carolina, Sch Med, Dept Cell Biol & Anat, Columbia, SC 29208 USA
[5] Stetson Univ, Dept Biol, Deland, FL 32724 USA
[6] Advent Hlth Univ, Dept Hlth & Biomed Sci, Orlando, FL 32803 USA
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2024年 / 12卷
关键词
Ciona intestinalis; myocardium; gene expression; cardiac myocyte; microarray; CHORDATE; HEART; EXPLORATION; SIGNALS; GENOME; MODEL; AKT;
D O I
10.3389/fcell.2024.1304755
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ciona intestinalis is an invertebrate animal model system that is well characterized and has many advantages for the study of cardiovascular biology. The regulatory mechanisms of cardiac myocyte proliferation in Ciona are intriguing since regeneration of functional tissue has been demonstrated in other organs of Ciona in response to injury. To identify genes that are differentially expressed in response to Ciona cardiac injury, microarray analysis was conducted on RNA from adult Ciona hearts with normal or damaged myocardium. After a 24- or 48-h recovery period, total RNA was isolated from damaged and control hearts. Initial results indicate significant changes in gene expression in hearts damaged by ligation in comparison to control hearts. Ligation injury shows differential expression of 223 genes as compared to control with limited false discovery (5.8%). Among these 223 genes, 117 have known human orthologs of which 68 were upregulated and 49 were downregulated. Notably, Fgf9/16/20, insulin-like growth factor binding protein and Ras-related protein Rab11b were significantly upregulated in injured hearts, whereas expression of a junctophilin ortholog was decreased. Histological analyses of injured myocardium were conducted in parallel to the microarray study which revealed thickened myocardium in injured hearts. Taken together, these studies will connect differences in gene expression to cellular changes in the myocardium of Ciona, which will help to promote further investigations into the regulatory mechanisms of cardiac myocyte proliferation across chordates.
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