Immunocytochemical distribution of WARP (von Willebrand A domain-related protein) in the inner ear
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- 作者：Trac Duong ; Ivan A. Lopez ; Akira Ishiyama ; Gail Ishiyama
- 关键词：VWA-1 ; Basement membrane ; Blood vessels ; Cochlea ; Extracellular matrix ; Inner ear microvasculature
- 刊名：Brain Research
- 出版年：2011
- 出版时间：7 January 2011
- 年：2011
- 卷：1367
- 期：Complete
- 页码：50-61
- 全文大小：2574 K
文摘
The basic components of the epithelial, perineural, and perivascular basement membranes in the inner ear have been well-documented in several animal models and in the human inner ear. The von Willebrand A domain-related protein (WARP) is an extracellular matrix molecule with restricted expression in cartilage, and a subset of basement membranes in peripheral nerves, muscle, and central nervous system vasculature. It has been suggested that WARP has an important role in maintaining the blood–brain barrier. To date no studies on WARP distribution have been performed in the inner ear, which is equipped with an intricate vasculature network. In the present study, we determined the distribution of WARP by immunocytochemistry in the human inner ear using auditory and vestibular endorgans microdissected from human temporal bones obtained at autopsy. All subjects (n = 5, aged 55–87 years old) had documented normal auditory and vestibular function. We also determined the WARP immunolocalization in the mouse inner ear. WARP immunoreactivity localized to the vasculature throughout the stroma of the cristae ampullaris, the maculae utricle, and saccule in the human and mouse. In the human and mouse inner ear, WARP immunoreactivity delineated blood vessels located in the stria vascularis, spiral ligament, sub-basilar region, stromal tissue, and the spiral and vestibular ganglia. The distinct localization of WARP in the inner ear vasculature suggests an important role in maintaining its integrity. In addition, WARP allows delineation of microvessels in the inner ear allowing the study of vascular pathology in the development of otological diseases.