Gaikwad Naina, Sarwade Rucha, Halder Sourav, Agarwal Gaurav, Seshadri Vasudevan
National Centre for Cell Science, Ganeshkhind, Pune, India.
Savitribai Phule Pune University, Ganeshkhind, Pune, India.
PLoS One. 2024 Dec 16;19(12):e0315535. doi: 10.1371/journal.pone.0315535. eCollection 2024.
HuD plays a critical role in neurite outgrowth, neuronal plasticity, and survival. However, HuD autoantibodies from patients with paraneoplastic gut dysmotility can trigger the apoptotic cascade in human neuroblastoma cell line and myenteric neurons. The mechanism by which HuD regulates the apoptotic pathway is unclear. Apoptosis is one of the underlying causes of neurodegenerative diseases like Alzheimer's disease. In the current study, we found that HuD interacts with Msi2 transcript and positively regulates it in the mouse neuroblastoma (N2a) cells. MSI2 being an RNA binding protein has diverse mRNA targets and regulates the mitochondrial apoptotic pathway by interacting with and repressing APAF1 transcript. Conversely, the reduced levels of HuD leads to decreased Msi2 expression and increased APAF1 levels, which results in apoptosis in N2a cells. Overall, our research indicates that HuD and Msi2 possess an anti-apoptotic role in N2A cells.
HuD在神经突生长、神经元可塑性和存活中发挥关键作用。然而,来自副肿瘤性肠道运动障碍患者的HuD自身抗体会触发人神经母细胞瘤细胞系和肌间神经元中的凋亡级联反应。HuD调节凋亡途径的机制尚不清楚。凋亡是阿尔茨海默病等神经退行性疾病的潜在病因之一。在本研究中,我们发现HuD与Msi2转录本相互作用,并在小鼠神经母细胞瘤(N2a)细胞中正向调节它。MSI2作为一种RNA结合蛋白,具有多种mRNA靶点,并通过与APAF1转录本相互作用并抑制它来调节线粒体凋亡途径。相反,HuD水平降低会导致Msi2表达下降和APAF1水平升高,从而导致N2a细胞凋亡。总体而言,我们的研究表明HuD和Msi2在N2A细胞中具有抗凋亡作用。