کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6276338 1614887 2011 14 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
All functional aquaporin-4 isoforms are expressed in the rat cochlea and contribute to the formation of orthogonal arrays of particles
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
All functional aquaporin-4 isoforms are expressed in the rat cochlea and contribute to the formation of orthogonal arrays of particles
چکیده انگلیسی

The water channel aquaporin-4 (AQP4) is expressed in the cochlea and is essential for normal hearing. Unlike other AQPs, multiple isoforms of AQP4 have been reported in diverse tissues, three of which, M1, M23, and Mz, function as water channels. In addition, these protein isoforms are found in higher order complexes. Morphologically these higher order complexes correspond to orthogonal arrays of particles (OAPs) that are found in cell membranes by freeze fracture analysis. Using RT-PCR, quantitative PCR and blue-native PAGE immunoblots we identified all functional AQP4 isoforms —M1, M23, and Mz— and the formation of higher-order complexes in the organ of Corti of the rat. Complementary freeze-fracture studies revealed OAPs distributed in the lateral and basal membrane domains of the cochlear duct supporting cells, specifically Hensen's cells and outer sulcus cells. The unique inter- and intracellular heterogeneity in size, density and shape of OAPs suggests exceptional physiological requirements for the maintenance of water homeostasis during auditory sensory transduction in the cochlea.

▶All functional AQP4 isoforms—M1, M23, and Mz—are identified in the cochlea. ▶All AQP4 isoforms contribute to a formation of higher order structures. ▶Freeze facture analysis shows the differential distribution of OAPs in distinct supporting cell types. ▶The organ of Corti shows a unique intra- and intercellular heterogeneity in size, density and shape of orthogonal arrays of particles.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 189, 25 August 2011, Pages 79–92