Compartmentalized ciliation changes of oligodendrocytes in aged mouse optic nerve

Abstract

AbstractPrimary cilia are microtubule‐based sensory organelles that project from the apical surface of most mammalian cells, including oligodendrocytes, which are myelinating cells of the central nervous system (CNS) that support critical axonal function. Dysfunction of CNS glia is associated with aging‐related white matter diseases and neurodegeneration, and ciliopathies are known to affect CNS white matter. To investigate age‐related changes in ciliary profile, we examined ciliary length and frequency in the retinogeniculate pathway, a white matter tract commonly affected by diseases of aging but in which expression of cilia has not been characterized. We found expression of Arl13b, a marker of primary cilia, in a small group of Olig2‐positive oligodendrocytes in the optic nerve, optic chiasm, and optic tract in young and aged C57BL/6 wild‐type mice. While the ciliary length and ciliated oligodendrocyte cells were constant in young mice in the retinogeniculate pathway, there was a significant increase in ciliary length in the anterior optic nerve as compared to the aged animals. Morphometric analysis confirmed a specific increase in the ciliation rate of CC1+/Olig2+ oligodendrocytes in aged mice compared with young mice. Thus, the prevalence of primary cilia in oligodendrocytes in the visual pathway and the age‐related changes in ciliation suggest that they may play important roles in white matter and age‐associated optic neuropathies.