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本文引用的文献

1
Longitudinal analysis of calorie restriction on rat taste bud morphology and expression of sweet taste modulators.热量限制对大鼠味蕾形态和甜味调制器表达的纵向分析。
J Gerontol A Biol Sci Med Sci. 2014 May;69(5):532-44. doi: 10.1093/gerona/glt129. Epub 2013 Sep 28.
2
Lgr5 Identifies Progenitor Cells Capable of Taste Bud Regeneration after Injury.Lgr5可识别损伤后能够进行味蕾再生的祖细胞。
PLoS One. 2013 Jun 18;8(6):e66314. doi: 10.1371/journal.pone.0066314. Print 2013.
3
Heterotrimeric G protein subunit Gγ13 is critical to olfaction.三聚体 G 蛋白亚基 Gγ13 对嗅觉至关重要。
J Neurosci. 2013 May 1;33(18):7975-84. doi: 10.1523/JNEUROSCI.5563-12.2013.
4
Pre-treatment with amifostine protects against cyclophosphamide-induced disruption of taste in mice.在用环磷酰胺预处理可以防止其引起的小鼠味觉障碍。
PLoS One. 2013 Apr 23;8(4):e61607. doi: 10.1371/journal.pone.0061607. Print 2013.
5
Neurosensory transmission without a synapse: new perspectives on taste signaling.无突触的神经感觉传递:味觉信号传导的新视角
BMC Biol. 2013 Apr 15;11:42. doi: 10.1186/1741-7007-11-42.
6
CALHM1 ion channel mediates purinergic neurotransmission of sweet, bitter and umami tastes.CALHM1 离子通道介导甜味、苦味和鲜味的嘌呤能神经递质传递。
Nature. 2013 Mar 14;495(7440):223-6. doi: 10.1038/nature11906. Epub 2013 Mar 6.
7
High salt recruits aversive taste pathways.高盐会招募厌恶味觉通路。
Nature. 2013 Feb 28;494(7438):472-5. doi: 10.1038/nature11905. Epub 2013 Feb 13.
8
Lgr5-EGFP marks taste bud stem/progenitor cells in posterior tongue.Lgr5-EGFP 标记舌后段的味蕾干细胞/祖细胞。
Stem Cells. 2013 May;31(5):992-1000. doi: 10.1002/stem.1338.
9
Functional cell types in taste buds have distinct longevities.味蕾中的功能性细胞类型具有不同的寿命。
PLoS One. 2013;8(1):e53399. doi: 10.1371/journal.pone.0053399. Epub 2013 Jan 8.
10
Expression and secretion of TNF-α in mouse taste buds: a novel function of a specific subset of type II taste cells.在小鼠味蕾中 TNF-α 的表达和分泌:特定类型 II 味觉细胞亚群的新功能。
PLoS One. 2012;7(8):e43140. doi: 10.1371/journal.pone.0043140. Epub 2012 Aug 14.

味蕾稳态:在健康、疾病和衰老中的作用。

Taste bud homeostasis in health, disease, and aging.

机构信息

Monell Chemical Senses Center, 3500 Market Street, Philadelphia, PA 19104, USA.

出版信息

Chem Senses. 2014 Jan;39(1):3-16. doi: 10.1093/chemse/bjt059. Epub 2013 Nov 28.

DOI:10.1093/chemse/bjt059
PMID:24287552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3864165/
Abstract

The mammalian taste bud is an onion-shaped epithelial structure with 50-100 tightly packed cells, including taste receptor cells, supporting cells, and basal cells. Taste receptor cells detect nutrients and toxins in the oral cavity and transmit the sensory information to gustatory nerve endings in the buds. Supporting cells may play a role in the clearance of excess neurotransmitters after their release from taste receptor cells. Basal cells are precursor cells that differentiate into mature taste cells. Similar to other epithelial cells, taste cells turn over continuously, with an average life span of about 8-12 days. To maintain structural homeostasis in taste buds, new cells are generated to replace dying cells. Several recent studies using genetic lineage tracing methods have identified populations of progenitor/stem cells for taste buds, although contributions of these progenitor/stem cell populations to taste bud homeostasis have yet to be fully determined. Some regulatory factors of taste cell differentiation and degeneration have been identified, but our understanding of these aspects of taste bud homoeostasis remains limited. Many patients with various diseases develop taste disorders, including taste loss and taste distortion. Decline in taste function also occurs during aging. Recent studies suggest that disruption or alteration of taste bud homeostasis may contribute to taste dysfunction associated with disease and aging.

摘要

哺乳动物的味蕾是一种洋葱状的上皮结构,由 50-100 个紧密排列的细胞组成,包括味觉受体细胞、支持细胞和基底细胞。味觉受体细胞检测口腔中的营养物质和毒素,并将感觉信息传递到味蕾中的味觉神经末梢。支持细胞在味觉受体细胞释放过多神经递质后可能发挥清除作用。基底细胞是一种前体细胞,可分化为成熟的味觉细胞。与其他上皮细胞一样,味觉细胞不断更新,平均寿命约为 8-12 天。为了维持味蕾的结构稳态,新的细胞会产生以取代死亡的细胞。最近使用遗传谱系追踪方法的几项研究已经确定了味觉细胞的祖细胞/干细胞群体,尽管这些祖细胞/干细胞群体对味觉细胞稳态的贡献尚未完全确定。已经鉴定出一些调节味觉细胞分化和退化的因子,但我们对味觉细胞稳态这些方面的理解仍然有限。许多患有各种疾病的患者会出现味觉障碍,包括味觉丧失和味觉失真。味觉功能的衰退也会随着年龄的增长而发生。最近的研究表明,味觉细胞稳态的破坏或改变可能与疾病和衰老相关的味觉功能障碍有关。