Furtado João, Bento Margaret, Correia Elizabeth, Inácio José Manuel, Belo José António
Regenerative Medicine Program, Departamento de Ciências Biomédicas e Medicina, Universidade do Algarve, Faro, Portugal; IBB-Institute for Biotechnology and Bioengineering, Centro de Biomedicina Molecular. e Estrutural, Universidade do Algarve, Campus de Gambelas, 8005-135 Faro, Portugal.
Regenerative Medicine Program, Departamento de Ciências Biomédicas e Medicina, Universidade do Algarve, Faro, Portugal; IBB-Institute for Biotechnology and Bioengineering, Centro de Biomedicina Molecular. e Estrutural, Universidade do Algarve, Campus de Gambelas, 8005-135 Faro, Portugal; CEDOC, NOVA Medical School/Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Campo Mártires da Pátria 130, 1169-056 Lisboa, Portugal.
PLoS One. 2014 Dec 29;9(12):e115481. doi: 10.1371/journal.pone.0115481. eCollection 2014.
During the course of a differential screen to identify transcripts specific for chick heart/hemangioblast precursor cells, we have identified Ccbe1 (Collagen and calcium-binding EGF-like domain 1). While the importance of Ccbe1 for the development of the lymphatic system is now well demonstrated, its role in cardiac formation remained unknown. Here we show by whole-mount in situ hybridization analysis that cCcbe1 mRNA is initially detected in early cardiac progenitors of the two bilateral cardiogenic fields (HH4), and at later stages on the second heart field (HH9-18). Furthermore, cCcbe1 is expressed in multipotent and highly proliferative cardiac progenitors. We characterized the role of cCcbe1 during early cardiogenesis by performing functional studies. Upon morpholino-induced cCcbe1 knockdown, the chick embryos displayed heart malformations, which include aberrant fusion of the heart fields, leading to incomplete terminal differentiation of the cardiomyocytes. cCcbe1 overexpression also resulted in severe heart defects, including cardia bifida. Altogether, our data demonstrate that although cardiac progenitors cells are specified in cCcbe1 morphants, the migration and proliferation of cardiac precursors cells are impaired, suggesting that cCcbe1 is a key gene during early heart development.
在一次差异筛选以鉴定鸡心脏/血管母细胞前体细胞特异性转录本的过程中,我们鉴定出了Ccbe1(胶原蛋白和钙结合表皮生长因子样结构域1)。虽然Ccbe1对淋巴系统发育的重要性现已得到充分证明,但其在心脏形成中的作用仍不清楚。在此我们通过整体原位杂交分析表明,cCcbe1 mRNA最初在两个双侧生心区的早期心脏祖细胞(HH4)中被检测到,在后期阶段则在第二心脏区(HH9 - 18)中被检测到。此外,cCcbe1在多能且高度增殖的心脏祖细胞中表达。我们通过进行功能研究来表征cCcbe1在早期心脏发生过程中的作用。在用吗啉代诱导cCcbe1敲低后,鸡胚胎出现心脏畸形,包括心脏区异常融合,导致心肌细胞不完全终末分化。cCcbe1过表达也导致严重的心脏缺陷,包括心脏裂。总之,我们的数据表明,虽然在cCcbe1 morphants中心脏祖细胞已被指定,但心脏前体细胞的迁移和增殖受到损害,这表明cCcbe1是早期心脏发育过程中的一个关键基因。