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转录因子间充质同源盒蛋白 2(MEOX2)调节伤害感受器功能。

Transcription factor mesenchyme homeobox protein 2 (MEOX2) modulates nociceptor function.

机构信息

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.

CeMM-Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.

出版信息

FEBS J. 2022 Jun;289(12):3457-3476. doi: 10.1111/febs.16347. Epub 2022 Feb 16.

Abstract

Mesenchyme homeobox protein 2 (MEOX2) is a transcription factor involved in mesoderm differentiation, including development of bones, muscles, vasculature and dermatomes. We have previously identified dysregulation of MEOX2 in fibroblasts from Congenital Insensitivity to Pain patients, and confirmed that btn, the Drosophila homologue of MEOX2, plays a role in nocifensive responses to noxious heat stimuli. To determine the importance of MEOX2 in the mammalian peripheral nervous system, we used a Meox2 heterozygous (Meox2 ) mouse model to characterise its function in the sensory nervous system, and more specifically, in nociception. MEOX2 is expressed in the mouse dorsal root ganglia (DRG) and spinal cord, and localises in the nuclei of a subset of sensory neurons. Functional studies of the mouse model, including behavioural, cellular and electrophysiological analyses, showed altered nociception encompassing impaired action potential initiation upon depolarisation. Mechanistically, we noted decreased expression of Scn9a and Scn11a genes encoding Na 1.7 and Na 1.9 voltage-gated sodium channels respectively, that are crucial in subthreshold amplification and action potential initiation in nociceptors. Further transcriptomic analyses of Meox2 DRG revealed downregulation of a specific subset of genes including those previously associated with pain perception, such as PENK and NPY. Based on these observations, we propose a novel role of MEOX2 in primary afferent nociceptor neurons for the maintenance of a transcriptional programme required for proper perception of acute and inflammatory noxious stimuli.

摘要

间质同源盒蛋白 2(MEOX2)是一种参与中胚层分化的转录因子,包括骨骼、肌肉、脉管系统和皮节的发育。我们之前已经在先天性疼痛不敏感患者的成纤维细胞中发现了 MEOX2 的失调,并证实了 Drosophila 同源物 btn 在伤害性热刺激的伤害性反应中发挥作用。为了确定 MEOX2 在哺乳动物周围神经系统中的重要性,我们使用 Meox2 杂合(Meox2 )小鼠模型来表征其在感觉神经系统中的功能,特别是在伤害感受中的功能。MEOX2 在小鼠背根神经节(DRG)和脊髓中表达,并定位于感觉神经元亚群的细胞核中。对小鼠模型的功能研究,包括行为、细胞和电生理分析,显示出伤害感受的改变,包括在去极化时动作电位起始受损。从机制上讲,我们注意到编码 Na 1.7 和 Na 1.9 电压门控钠离子通道的 Scn9a 和 Scn11a 基因的表达减少,这些基因在伤害感受器的亚阈值放大和动作电位起始中至关重要。对 Meox2 DRG 的进一步转录组分析显示,包括先前与疼痛感知相关的基因在内的特定基因子集下调,如 PENK 和 NPY。基于这些观察结果,我们提出了 MEOX2 在初级传入伤害感受器神经元中的新作用,用于维持适当感知急性和炎症性伤害性刺激所需的转录程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c81/9306780/430522fccdb8/FEBS-289-3457-g005.jpg

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