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神经元3',3,5-三碘甲状腺原氨酸(T3)摄取以及Mct8基因缺陷小鼠的行为表型,Mct8是在艾伦-赫ndon-达德利综合征中发生突变的神经元T3转运体。

Neuronal 3',3,5-triiodothyronine (T3) uptake and behavioral phenotype of mice deficient in Mct8, the neuronal T3 transporter mutated in Allan-Herndon-Dudley syndrome.

作者信息

Wirth Eva K, Roth Stephan, Blechschmidt Cristiane, Hölter Sabine M, Becker Lore, Racz Ildiko, Zimmer Andreas, Klopstock Thomas, Gailus-Durner Valerie, Fuchs Helmut, Wurst Wolfgang, Naumann Thomas, Bräuer Anja, de Angelis Martin Hrabé, Köhrle Josef, Grüters Annette, Schweizer Ulrich

机构信息

Neuroscience Research Center, Charité Universitätsmedizin Berlin, Berlin, Germany.

出版信息

J Neurosci. 2009 Jul 29;29(30):9439-49. doi: 10.1523/JNEUROSCI.6055-08.2009.

Abstract

Thyroid hormone transport into cells requires plasma membrane transport proteins. Mutations in one of these, monocarboxylate transporter 8 (MCT8), have been identified as underlying cause for the Allan-Herndon-Dudley syndrome, an X-linked mental retardation in which the patients also present with abnormally high 3',3,5-triiodothyronine (T(3)) plasma levels. Mice deficient in Mct8 replicate the thyroid hormone abnormalities observed in the human condition. However, no neurological deficits have been described in mice lacking Mct8. Therefore, we subjected Mct8-deficient mice to a comprehensive immunohistochemical, neurological, and behavioral screen. Several behavioral abnormalities were found in the mutants. Interestingly, some of these behavioral changes are compatible with hypothyroidism, whereas others rather indicate hyperthyroidism. We thus hypothesized that neurons exclusively dependent on Mct8 are in a hypothyroid state, whereas neurons expressing other T(3) transporters become hyperthyroid, if they are exposed directly to the high plasma T(3). The majority of T(3) uptake in primary cortical neurons is mediated by Mct8, but pharmacological inhibition suggested functional expression of additional T(3) transporter classes. mRNAs encoding six T(3) transporters, including L-type amino acid transporters (LATs), were coexpressed with Mct8 in isolated neurons. We then demonstrated Lat2 expression in cultured neurons and throughout murine brain development. In contrast, LAT2 is expressed in microglia in the developing human brain during gestation, but not in neurons. We suggest that lack of functional complementation by alternative thyroid hormone transporters in developing human neurons precipitates the devastating neurodevelopmental phenotype in MCT8-deficient patients, whereas Mct8-deficient mouse neurons are functionally complemented by other transporters, for possibly Lat2.

摘要

甲状腺激素进入细胞需要质膜转运蛋白。其中一种单羧酸转运蛋白8(MCT8)的突变已被确定为艾伦 - 赫恩登 - 达德利综合征的根本原因,这是一种X连锁智力障碍,患者还表现出异常高的3',3,5 - 三碘甲状腺原氨酸(T(3))血浆水平。缺乏Mct8的小鼠重现了人类疾病中观察到的甲状腺激素异常。然而,尚未在缺乏Mct8的小鼠中描述神经功能缺损。因此,我们对缺乏Mct8的小鼠进行了全面的免疫组织化学、神经学和行为学筛查。在突变体中发现了几种行为异常。有趣的是,其中一些行为变化与甲状腺功能减退相符,而其他变化则更表明甲状腺功能亢进。因此,我们推测完全依赖Mct8的神经元处于甲状腺功能减退状态,而表达其他T(3)转运蛋白的神经元如果直接暴露于高血浆T(3)中则会变为甲状腺功能亢进。原代皮质神经元中大部分T(3)摄取由Mct8介导,但药理学抑制表明还存在其他功能表达的T(3)转运蛋白类别。编码六种T(3)转运蛋白的mRNA,包括L型氨基酸转运蛋白(LATs),在分离的神经元中与Mct8共表达。然后我们证明了Lat2在培养的神经元以及整个小鼠脑发育过程中的表达。相比之下,LAT2在妊娠期间发育中的人类大脑的小胶质细胞中表达,但在神经元中不表达。我们认为,发育中的人类神经元中缺乏替代甲状腺激素转运蛋白的功能互补导致了MCT8缺陷患者中毁灭性的神经发育表型,而缺乏Mct8的小鼠神经元在功能上由其他转运蛋白(可能是Lat2)互补。

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