Affiliations: [a] Department of Otolaryngology, University of Texas Medical Branch, Galveston, Texas | [b] Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston, Texas | [c] Department of Anatomy and Neuroscience, University of Texas Medical Branch, Galveston, Texas
Correspondence:
[*]
Correspondence should be sent to Anthony J. Ricci, Ph.D., University of Wisconsin, Department of Neurophysiology, 273 Medical Science Center, 1300 University Ave., Madison, WI 53706; Tel.: (608) 262-9320.
Note: [**] Reprint address: Manning J. Correia, PhD., Department of Otolaryngology, University of Texas Medical Branch, 7.102 Medical Research Building, Galveston, TX 77555-1063.
Abstract: Classically, type I and type II vestibular hair cells have been defined by their afferent innervation patterns. Little quantitative information exists on the intrinsic morphometric differences between hair cell types. Data presented here define a quantitative method for distinguishing hair cell types based on the morphometric properties of the hair cell’s neck region. The method is based initially on fixed histological sections, where hair cell types were identified by innervation pattern, type I cells having an afferent calyx. Cells were viewed using light microscopy, images were digitized, and measurements were made of the cell body width, the cuticular plate width, and the neck width. A plot of the ratio of the neck width to cuticular plate width (NPR) versus the ratio of the neck width to the body width (NBR) established four quadrants based on the best separation of type I and type II hair cells. The combination of the two variables made the accuracy of predicting either type I or type II hair cells greater than 90%. Statistical cluster analysis confirmed the quadrant separation. Similar analysis was performed on dissociated hair cells from semicircular canal, utricle, and lagena, giving results statistically similar to those of the fixed tissue. Additional comparisons were made between fixed tissue and isolated hair cells as well as across species (pigeon and gerbil) and between end organs (semicircular canal, utricle, and lagena). In each case, the same morphometric boundaries could be used to establish four quadrants, where quadrant 1 was predominantly type I cells and quadrant 3 was almost exclusively type II hair cells. The quadrant separations were confirmed statistically by cluster analysis. These data demonstrate that there are intrinsic morphometric differences between type I and type II hair cells and that these differences can be maintained when the hair cells are dissociated from their respective epithelia.
