Centre of Marine Sciences (CCMAR), University of Algarve, Campus de Gambelas, 8005-139, Faro, Portugal.
Centre for Ocean Research, Sathyabama Institute of Science and Technology, Jeppiaar Nagar, Rajiv Gandhi Salai, Chennai, Tamil Nadu, 600 119, India.
Mar Biotechnol (NY). 2020 Jun;22(3):333-347. doi: 10.1007/s10126-019-09937-3. Epub 2020 Feb 20.
Teleosts have the ability to regenerate their caudal fin upon amputation. A highly proliferative mass of undifferentiated cells called blastema forms beneath wound epidermis and differentiates to regenerate all missing parts of the fin. To date, the origin and fate of the blastema is not completely understood. However, current hypotheses suggest that the blastema is comprised of lineage-restricted dedifferentiated cells. To investigate the differentiation capacity of regenerating fin-derived cells, primary cultures were initiated from the explants of 2-days post-amputation (dpa) regenerates of juvenile gilthead seabream (Sparus aurata). These cells were subcultured for over 30 passages and were named as BSa2. After 10 passages they were characterized for their ability to differentiate towards different bone cell lineages and mineralize their extracellular matrix, through immunocytochemistry, histology, and RT-PCR. Exogenous DNA was efficiently delivered into these cells by nucleofection. Assessment of lineage-specific markers revealed that BSa2 cells were capable of osteo/chondroblastic differentiation. BSa2 cells were also found to be capable of osteoclastic differentiation, as demonstrated through TRAP-specific staining and pit resorption assay. Here, we describe the development of the first successful cell line viz., BSa2, from S. aurata 2-dpa regenerating caudal fins, which has the ability of multilineage differentiation and is capable of in vitro mineralization. The availability of such in vitro cell systems has the potential to stimulate research on the mechanisms of cell differentiation during fin regeneration and provide new insights into the mechanisms of bone formation.
硬骨鱼类具有在尾部受伤后再生的能力。在伤口表皮下会形成一个叫做芽基的高度增殖的未分化细胞团,这些细胞会分化以再生尾部所有缺失的部分。迄今为止,芽基的起源和命运还不完全清楚。然而,目前的假说表明,芽基由谱系受限的去分化细胞组成。为了研究再生鳍衍生细胞的分化能力,从幼年金头鲷(Sparus aurata) 2 天断尾再生体的外植体中启动了原代培养。这些细胞被传代培养超过 30 代,并被命名为 BSa2。在传代 10 次后,通过免疫细胞化学、组织学和 RT-PCR 对它们向不同骨细胞谱系分化和矿化细胞外基质的能力进行了表征。通过核转染将外源性 DNA 有效地递送到这些细胞中。谱系特异性标志物的评估表明,BSa2 细胞能够向成骨/软骨细胞分化。通过 TRAP 特异性染色和陷窝吸收测定还发现 BSa2 细胞具有破骨细胞分化的能力。在这里,我们描述了第一个成功的细胞系 BSa2 的开发,该细胞系来自 S. aurata 2 天断尾再生的尾部,具有多谱系分化的能力,并能够在体外矿化。这种体外细胞系统的可用性有可能刺激对鳍再生过程中细胞分化机制的研究,并为骨形成的机制提供新的见解。