Ceder Mikaela M, Lekholm Emilia, Hellsten Sofie V, Perland Emelie, Fredriksson Robert
Molecular Neuropharmacology, Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Front Mol Neurosci. 2017 Oct 31;10:351. doi: 10.3389/fnmol.2017.00351. eCollection 2017.
Many transporters such as the solute carriers belonging to the Major facilitator superfamily Pfam clan are orphans in that their tissue and cellular localization as well as substrate profile and function are still unknown. Here we have characterized the putative solute carrier UNC93A. We aimed to investigate the expression profile on both protein and mRNA level of UNC93A in mouse since it has not been clarified. UNC93A staining was found in cortex, hippocampus and cerebellum. It was found to be expressed in many neurons, but not all, with staining located in close proximity to the plasma membrane. Furthermore, we aimed to extend the starvation data available for in hypothalamic cell cultures from mouse. We investigated the alterations with focus on amino acid deprivation in embryonic cortex cells from mice as well as 24 h starvation in adult male mice and compared it to recently studied putative and known solute carriers. expression was found both in the brain and peripheral organs, in low to moderate levels in the adult mice and was affected by amino acid deprivation in embryonic cortex cultures and starvation in samples. In conclusion, the membrane-bound UNC93A is expressed in both the brain and peripheral tissues and responds to nutrient availability in mice.
许多转运蛋白,如属于主要易化子超家族Pfam家族的溶质载体,都是“孤儿”,因为它们在组织和细胞中的定位以及底物谱和功能仍然未知。在这里,我们对推定的溶质载体UNC93A进行了表征。由于尚未阐明,我们旨在研究UNC93A在小鼠体内蛋白质和mRNA水平上的表达谱。在皮质、海马体和小脑中发现了UNC93A染色。发现它在许多神经元中表达,但不是所有神经元,染色位于靠近质膜的位置。此外,我们旨在扩展小鼠下丘脑细胞培养中可用的饥饿数据。我们研究了小鼠胚胎皮质细胞中氨基酸剥夺以及成年雄性小鼠24小时饥饿后的变化,并将其与最近研究的推定和已知溶质载体进行了比较。在成年小鼠的大脑和外周器官中均发现了表达,水平低至中等,并且在胚胎皮质培养中的氨基酸剥夺和样本饥饿中受到影响。总之,膜结合的UNC93A在大脑和外周组织中均有表达,并对小鼠体内的营养供应作出反应。