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Differential gene expression of 36-kDa microfibril-associated glycoprotein (MAGP-36/MFAP4) in rat organs
Authors:Tetsuhiko Toyoshima  Tetsuya Ishida  Nozomu Nishi  Ryoji Kobayashi  Takehiro Nakamura  Toshifumi Itano
Institution:(1) Department of Structure and Functional Medicine, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kagawa 761-0793, Japan;(2) Department of Histology and Cell Biology, Faculty of Medicine, Kagawa University, Ikenobe, Miki-cho, Kagawa 761-0793, Japan;(3) Department of Endocrinology, Faculty of Medicine, Kagawa University, Ikenobe, Miki-cho, Kagawa 761-0793, Japan;(4) Department of Signal Transduction Sciences, Faculty of Medicine, Kagawa University, Ikenobe, Miki-cho, Kagawa 761-0793, Japan
Abstract:By using quantitative Western blot analysis and the real time polymerase chain reaction technique, we investigated the differential gene expression of microfibril-associated glycoprotein (MAGP-36) in rat organs. The gene was expressed highly in sites rich in elastic fibers, such as aorta, skin, and esophagus. However, MAGP-36 was also expressed highly in some other sites containing no elastic fibers. In lung and trachea, the expression levels of MAGP-36 mRNA were about seven times higher than those in other elastic tissues, although the protein abundances were almost at the same levels as other elastic tissues. MAGP-36 seemed to be secreted outside these organs. In brain, kidney, and spleen, although the expression levels of MAGP-36 mRNA were low, substantial amounts of MAGP-36 protein were detected. An immunohistochemical study revealed that MAGP-36 was present at the brush border of the S3 segment of proximal tubules in kidney. Since MAGP-36 is known to bind to mannan, MAGP-36 might be involved in mannose transport in the S3 segment. Thus, MAGP-36 might be multifunctional and present in a wide variety of sites in various organs.
Keywords:MAGP-36  MFAP4  AAAP-40  Smith-Magenis syndrome  S3  Mannose  Rat (Sprague Dawley)
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