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Genetic Labeling of Tas1 r 1 and Tas2r131 Taste Receptor Cells in Mice

机译:Tas1 r 1和Tas2r131味觉小鼠细胞的遗传标记。

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摘要

Characterization of the peripheral taste system relies on the identification and visualization of the different taste bud cell types. So far, genetic strategies to label taste receptor cells are limited to sweet, sour, and salty detecting cells. To visualize Tas1 r 1 umami and Tas2r131 bitter sensing cells, we generated animals in which the Tas1 r 1 and Tas2r131 open reading frames are replaced by expression cassettes containing the fluorescent proteins mCherry or hrGFP, respectively. These animals enabled us to visualize and quantify the entire oral Tas1 r 1 and Tas2r131 cell populations. Tas1 r 1-mCherry cells were predominantly detected in fungiform papillae, whereas Tas2r131-hrGFP cells, which are ~4-fold more abundant, were mainly present in foliate and vallate papillae. In the palate, both cell types were similarly distributed. Mice carrying both recombinant alleles demonstrated completely segregated Tas1 r 1 and Tas2r131 cell populations. Only ~50% of the entire bitter cell population expressed hrGFP, indicating that bitter taste receptor cells express a subset of the bitter receptor repertoire. In extragustatory tissues, mCherry fluorescence was observed in testis and hrGFP fluorescence in testis, thymus, vomeronasal organ, and respiratory epithelium, suggesting that only few extraoral sites express Tas2r131 and Tas1 r 1 receptors at levels comparable to taste tissue.
机译:外围味觉系统的表征依赖于不同味蕾细胞类型的识别和可视化。到目前为止,标记味觉受体细胞的遗传策略仅限于甜,酸和咸的检测细胞。为了可视化Tas1 r 1鲜味和Tas2r131苦味感测细胞,我们生成了动物,其中Tas1 r 1和Tas2r131开放阅读框分别被包含荧光蛋白mCherry或hrGFP的表达盒取代。这些动物使我们能够可视化和量化整个口腔Tas1 r 1和Tas2r131细胞群体。 Tas1 r 1-mCherry细胞主要在真菌状乳头中检测到,而Tas2r131-hrGFP细胞则是约4倍的丰富,主要存在于叶状和valate状乳突中。在上颚中,两种细胞类型均相似地分布。携带两个重组等位基因的小鼠表现出完全分离的Tas1 r 1和Tas2r131细胞群体。整个苦味细胞群体中只有约50%表达了hrGFP,这表明苦味受体细胞表达了苦味受体库的一个子集。在味蕾外组织中,在睾丸中观察到mCherry荧光,在睾丸,胸腺,犁鼻器和呼吸道上皮中观察到hrGFP荧光,这表明只有很少的口腔外部位以与味觉组织相当的水平表达Tas2r131和Tas1r 1受体。

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