Differential expression of cytoskeletal genes in the cochlear nucleus

• Published in: The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology Vol. 288A; no. 4; pp. 447 - 465
• Main Authors: Friedland, David R., Popper, Paul, Eernisse, Rebecca, Ringger, Benjamin, Cioffi, Joseph A.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-04-2006
• Subjects: Animals; cochlear nucleus; Cochlear Nucleus - metabolism; Cochlear Nucleus - physiology; Cytoskeletal Proteins - metabolism; cytoskeleton; Cytoskeleton - physiology; Female; gene expression; Gene Expression Profiling; In Situ Hybridization; microarray; neurofilament; Rats; serial analysis of gene expression
• ISSN: 1552-4884; 1552-4892
• DOI: 10.1002/ar.a.20303

The relationship between structure and function is clearly illustrated by emerging evidence demonstrating the role of the neuronal cytoskeleton in physiological processes. For example, alterations in axonal caliber, a feature of the cytoskeleton, have been shown to affect reflex arc latencies and are prominent features of several neuropathological disorders. Even in the nonpathologic situation, however, axonal diameter may be a crucial element for the normal function of specialized auditory neurons. To investigate this relationship, we used serial analysis of gene expression and microarray analyses to characterize the expression of cytoskeletal genes in the central auditory system. These data, confirmed by real‐time RT‐PCR, identified differential expression of intermediate neurofilament transcripts (i.e., Nefh, Nef3, and Nfl) among the subdivisions of the cochlear nucleus. In situ hybridization was used to identify specific classes of neurons within the cochlear nucleus expressing these neurofilament genes. Robust neurofilament expression was seen in bushy cells and cochlear nerve root neurons, suggesting an association between cytoskeletal structure and rapid conduction velocities. Gene expression data were also identified for other classes of cytoskeletal and structural genes important in neuronal function. These results may help to explain some causes of hearing loss in hereditary neuropathies and provide an anatomic basis for understanding normal neuronal function in the central auditory system. Anat Rec Part A, 2006. © 2006 Wiley‐Liss, Inc.