PIWI-interacting RNA (piRNA) signatures in human cardiac progenitor cells

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• 作者：Serena Vella^a ; ^b ; ^{sevella@ismett.edu" class="auth_mail" title="E-mail the corresponding author} ; Alessia Gallo^a ; ^b ; Antonio Lo Nigro^b ; Daniele Galvagno^a ; ^b ; Giuseppe Maria Raffa^c ; Michele Pilato^c ; Pier Giulio Conaldi^a ; ^b
• 关键词：MI ; myocardial infarction ; CPC ; cardiac progenitor cells ; CS ; cardiospheres ; CDC ; cardiosphere-derived cells ; ncRNA ; non-coding RNA ; piRNA ; PIWI-interacting RNA ; CF ; cardiac fibroblasts ; RT ; retrotransposons
• 刊名：International Journal of Biochemistry and Cell Biology
• 出版年：2016
• 出版时间：July 2016
• 年：2016
• 卷：76
• 期：Complete
• 页码：1-11
• 全文大小：2889 K

文摘

Cardiac progenitors, such as cardiospheres and cardiosphere-derived cells, represent an attractive cell source for cardiac regeneration. The PIWI-interacting RNAs, piRNAs, are an intriguing class of small non-coding RNAs, implicated in the regulation of epigenetic state, maintenance of genomic integrity and stem cell functions. Although non-coding RNAs are an exploiting field in cardiovascular research, the piRNA signatures of cardiac progenitors has not been evaluated yet.We profiled, through microarrays, 15,311 piRNAs expressed in cardiospheres, cardiosphere-derived cells and cardiac fibroblasts. Results showed a set of differentially expressed piRNAs (fold change ≥2, p < 0.01): 641 piRNAs were upregulated and 1,301 downregulated in the cardiospheres compared to cardiosphere-derived cells, while 255 and 708 piRNAs resulted up- and down-regulated, respectively, if compared to cardiac fibroblasts. We also identified 181 piRNAs that are overexpressed and 129 are downregulated in cardiosphere-derived cells respect to cardiac fibroblasts.Bioinformatics analysis showed that the deregulated piRNAs were mainly distributed on few chromosomes, suggesting that piRNAs are organized in discrete genomic clusters.Furthermore, the bioinformatics search showed that the most upregulated piRNAs target transposons, especially belonged to LINE-1 class, as validated by qRT-PCR. This reduction is also associated to an activation of AKT signaling, which is beneficial for cardiac regeneration.The present study is the first to show a highly consistent piRNA expression pattern for human cardiac progenitors, likely responsible of their different regenerative power. Moreover, this piRNome analysis may provide new methods for characterize cardiac progenitors and may shed new light on the understanding the complex molecular mechanisms of cardiac regeneration.