Written in the Stars: Astrocyte Biology From Evolution to Disease
Carmen Falcone, Lutgarde Arckens, Monica Baiula, Andrea Bedini, Riccardo Bocchi, Matthew J. Broadhead, Marco Caprini, Fabio Cavaliere, Fabrizia Cesca, Helena H. Chowdhury, Katarzyna Ciuba, Laura Civiero, Carole Escartin, Stefano Ferroni, Francesco Formaggio, Angelisa Frasca, Rossella Gratton, Matthew Holt, Nunzio Iraci, Marko Kreft, Loredana Leggio, Annamaria Lia, Anna R. Malik, Rogier Min, Franziska E. Müller, Cahuê Murat, Maria João Pereira, Aleksandra Pekowska, Francesco Petrelli, Paula Ramos‐Gonzalez, Maria V. Sanchez‐Mico, Zala Smole, Dimitra Sokolova, Maite Solas, Alessia Soldano, Lukasz Mateusz Szewczyk, Carola Torazza, Francesco Paolo Ulloa Severino, Nerea Urrestizala‐Arenaza, Andre Zeug, Jiafeng Zhou, Micaela Zonta, Robert Zorec, Alexei Verkhratsky, Nilhan GunhanlarABSTRACT
In the 21st century, neuroglial research has entered a period of Renaissance, extending the views of prominent neuroanatomists and neurologists of the 19th and early 20th centuries, who assigned to glial cells numerous physiological functions and highlighted their fundamental role in the pathophysiology of nervous system diseases. Astrocytes are highly diversified in structure and function; they control brain homeostasis, support synaptic connectivity, and enable information processing in neural networks. Evolutionary diversification of astrocytes, initially emerging as supportive cells of primitive sensory organs, drove a continuous expansion of astroglial complexity and functional versatility, ultimately making them indispensable neuroprotectors and homeostatic regulators. The large, morphologically elaborate astrocytes of the human brain arguably reflect an evolutionary response to increased neuronal homeostatic demands. Astrocytes are indispensable for synaptic function, serving as the principal regulators of neurotransmitter turnover and neuronal excitability. Astrocytes also govern brain energy metabolism, mitochondrial dynamics, and calcium signaling, thereby actively shaping cortical plasticity and circuits. Astrocytes are fundamental elements of the pathophysiology of neurological, neuropsychiatric, and neurodegenerative diseases, including Alzheimer's and Parkinson's disease, amyotrophic lateral sclerosis, Rett syndrome, genetic astrocytopathies, and neurotrauma, where they demonstrate complex reactive changes directed at tissue preservation and regeneration, but which can also contribute to disease progression. Advances in single‐cell transcriptomics, calcium imaging, chemogenetics, and iPSC‐based models have transformed our understanding of astrocyte diversity and disease‐specific dysfunction, opening new avenues of investigation. Given that no CNS disorder is known to occur without astrocyte involvement, multiple astrocyte‐specific molecules represent compelling targets for cell‐directed therapeutic strategies.