کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6263378 1613882 2014 14 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research ReportPAT4 is abundantly expressed in excitatory and inhibitory neurons as well as epithelial cells
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Research ReportPAT4 is abundantly expressed in excitatory and inhibitory neurons as well as epithelial cells
چکیده انگلیسی


- PAT4 has abundant expression in neurons but not in astrocytes or glia cells in the mouse brain.
- PAT4 expression is mainly intracellular.
- PAT4 expression is also found in the plasma membrane of epithelial cells in choroid plexus.
- We show that the PAT family os evolutionary old and that PAT4 is the oldest member.

PAT4, the fourth member of the SLC36/proton dependent amino acid transporter (PAT) family, is a high-affinity, low capacity electroneutral transporter of neutral amino acids like proline and tryptophan. It has also been associated with the function of mTORC1, a complex in the mammalian target of rapamycin (mTOR) pathway. We performed in situ hybridization and immunohistological analysis to determine the expression profile of PAT4, as well as an RT-PCR study on tissue from mice exposed to leucine. We performed a phylogenetic analysis to determine the evolutionary origin of PAT4. The in situ hybridization and the immunohistochemistry on mouse brain sections and hypothalamic cells showed abundant PAT4 expression in the mouse brain intracellularly in both inhibitory and excitatory neurons, partially co-localizing with lysosomal markers and epithelial cells lining the ventricles. Its location in epithelial cells around the ventricles indicates a transport of substrates across the blood brain barrier. Phylogenetic analysis showed that PAT4 belongs to an evolutionary old family most likely predating animals, and PAT4 is the oldest member of that family.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1557, 4 April 2014, Pages 12-25
نویسندگان
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