Bagnoli Sara, Drago Davide Lorenzo, Astoricchio Emanuele, Chiavacci Elena, Fronte Baldassarre, Cellerino Alessandro, Terzibasi Tozzini Eva
Biology Laboratory (BIO@SNS), Scuola Normale Superiore, 56126 Pisa, Italy.
Biology and Evolution of Marine Organisms Department (BEOM), Stazione Zoologica Anton Dohrn, 80121 Napoli, Italy.
Int J Mol Sci. 2025 Apr 10;26(8):3563. doi: 10.3390/ijms26083563.
Adult neurogenesis in cartilaginous fish remains a relatively unexplored area, particularly in terms of comparative analysis. This process, defined as the ability of specialized stem cells to generate new functional neurons, has gained prominence due to its relevance in neurodegenerative disease research and regenerative medicine. However, there is an ongoing discussion about when and where it first appeared. Evidence of adult neurogenesis in both teleosts and mammals highlights significant differences, such as the number of newly formed cells and the brain regions involved. Investigating additional cartilaginous fish species, which occupy a basal position in vertebrate phylogeny, could provide valuable insights into the ancient origins of this trait and potentially new general knowledge about the adult neurogenesis process. In this study, we combined immunohistochemistry and in situ hybridization to examine neurogenic activity in three brain regions-the telencephalon, mesencephalon, and cerebellum-of two batoid species: and . Immunohistochemical methods were used to identify neurogenic cells by employing markers for cell proliferation (PCNA), mitosis (pH3), glial cells (S100B), and stem cells (Msi1). Additionally, in situ hybridization was performed to detect neural stem cell mRNA for , , and in the telencephalon and mesencephalon of .
软骨鱼类的成体神经发生仍然是一个相对未被探索的领域,尤其是在比较分析方面。这个过程被定义为特化干细胞产生新的功能性神经元的能力,由于其在神经退行性疾病研究和再生医学中的相关性而受到关注。然而,关于它首次出现的时间和地点仍在进行讨论。硬骨鱼和哺乳动物中成年神经发生的证据突出了显著差异,例如新形成细胞的数量和涉及的脑区。研究在脊椎动物系统发育中处于基础地位的其他软骨鱼类物种,可能会为这一特征的古老起源提供有价值的见解,并有可能获得关于成年神经发生过程的新的一般知识。在这项研究中,我们结合免疫组织化学和原位杂交技术,检测了两种魟类物种(和)三个脑区(端脑、中脑和小脑)的神经发生活性。免疫组织化学方法通过使用细胞增殖标记物(PCNA)、有丝分裂标记物(pH3)、神经胶质细胞标记物(S100B)和干细胞标记物(Msi1)来识别神经发生细胞。此外,我们还进行了原位杂交,以检测魟类端脑和中脑中、和的神经干细胞mRNA。