Singh Sneha, Kumar Ujendra
Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, BC, Canada.
Mol Neurobiol. 2025 Jul 2. doi: 10.1007/s12035-025-05179-8.
G-protein-coupled receptors (GPCRs) regulate multiple cellular functions, including neurite formation and maturation, processes often disrupted in neurodegenerative diseases. Like GPCRs, microtubule-associated proteins (MAPs, including MAP2 and Tuj1) and the synaptic vesicle protein synaptophysin are essential for neurite formation, maturation, and organization, which underpin brain development and cognitive function. Despite their importance, the functional crosstalk between GPCRs and MAPs, particularly in neurogenesis and pathological conditions such as Alzheimer's disease (AD), remains poorly understood. We show that somatostatin and dopamine receptors (SSTR and DR) are the structural anchors in developing neurites, enabling MAP recruitment and synaptic protein localization. Our findings reveal a cAMP-dependent interplay involving PTEN and ERK1/2, modulating neurite formation and MAPs organization. Notably, we show that β-amyloid (Aβ) disrupts the constitutive association of MAP2 and Tuj1, inducing an increase in intracellular cAMP levels, loss of neurite integrity, and impaired neuronal viability. The activation of SSTR and DR signaling restores neurite architecture and synaptic integrity via p-AKT activation and PTEN inhibition, highlighting a neuroprotective mechanism. Together, our results reveal a novel role of GPCRs in orchestrating interactions with MAPs to regulate neuronal maturation, neurite formation, and synaptic integrity. This study provides a new mechanistic rationale for therapeutic strategies aimed at preserving cognitive function in neurological disorders such as AD.
G蛋白偶联受体(GPCRs)调节多种细胞功能,包括神经突的形成和成熟,而这些过程在神经退行性疾病中常常受到破坏。与GPCRs一样,微管相关蛋白(MAPs,包括MAP2和Tuj1)以及突触小泡蛋白突触素对于神经突的形成、成熟和组织至关重要,这些过程是大脑发育和认知功能的基础。尽管它们很重要,但GPCRs与MAPs之间的功能相互作用,尤其是在神经发生和诸如阿尔茨海默病(AD)等病理状况下的相互作用,仍知之甚少。我们发现生长抑素和多巴胺受体(SSTR和DR)是发育中神经突的结构锚定物,能够招募MAPs并使突触蛋白定位。我们的研究结果揭示了一种涉及PTEN和ERK1/2的cAMP依赖性相互作用,调节神经突形成和MAPs组织。值得注意的是,我们发现β-淀粉样蛋白(Aβ)破坏了MAP2和Tuj1的组成性结合,导致细胞内cAMP水平升高、神经突完整性丧失以及神经元活力受损。SSTR和DR信号的激活通过p-AKT激活和PTEN抑制恢复神经突结构和突触完整性,突出了一种神经保护机制。总之,我们的结果揭示了GPCRs在协调与MAPs的相互作用以调节神经元成熟、神经突形成和突触完整性方面的新作用。这项研究为旨在保留诸如AD等神经疾病中认知功能的治疗策略提供了新的机制依据。