Abstract
AbstractSound information is transmitted from the cochlea to the brain mainly by type I spiral ganglion neurons (SGNs), which consist of different subtypes with distinct physiological properties and selective expression of molecular markers. It remains unclear how these SGN subtypes distribute along the tonotopic axis, and how the distribution pattern changes during aging that might underlie age-related hearing loss (ARHL). We investigated these questions using immunohistochemistry in three age groups of CBA/CaJ mice of either sex, including 2-5 months (young), 17-19 months (middle-age), and 28-32 months (old). Mouse cochleae were cryo-sectioned and triple-stained using antibodies against Tuj1, calretinin (CR) and calbindin (CB), which are reportedly expressed in all type I, subtype Ia, and subtype IbSGNs, respectively. Labeled SGNs were classified into four groups based on the expression pattern of stained markers, including CR+(subtype Ia), CB+(subtype Ib), CR+CB+(dual-labeled Ia/Ib), and CR-CB-(subtype Ic) neurons. The distribution of these SGN groups was analyzed in the apex, middle, and base regions of the cochleae. It showed that the prevalence of subtype Ia, Iband dual-labeled Ia/IbSGNs are high in the apex and low in the base. In contrast, the distribution pattern is reversed in IcSGNs. Such frequency-dependent distribution is largely maintained during aging except for a preferential reduction of IcSGNs, especially in the base. These findings suggest that sound processing of different frequencies involves distinct combinations of SGN subtypes, and the age-dependent loss of IcSGNs in the base may especially impact high-frequency hearing during ARHL.
Publisher
Cold Spring Harbor Laboratory