GDNF家族受体α样(GFRAL)的表达仅限于尾侧脑干。

IF 7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Cecilia Hes , Lu Ting Gui , Alexandre Bay , Fernando Alvarez , Pierce Katz , Tanushree Paul , Nadejda Bozadjieva-Kramer , Randy J. Seeley , Ciriaco A. Piccirillo , Paul V. Sabatini
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引用次数: 0

摘要

目的:生长分化因子15 (GDF15)作用于GDNF家族受体α样(GFRAL)受体二聚体,并在转染(RET)过程中重排。虽然已知表达Gfral的细胞存在于脑干的后脑区和孤立束核(AP/NTS),但在中枢神经系统和外周组织的其他部位表达Gfral的细胞的存在尚未得到充分解决。我们的目的是彻底研究GFRAL是否在外周组织和不同于脑干的脑部位表达。方法:从Gfral: eGFP小鼠中收集了包括脑在内的12种不同组织的组织,并使用单分子原位杂交技术鉴定这些组织中表达Gfral的细胞。然后,通过分析公开的单细胞RNA测序数据,我们将结果与人类gfral表达进行了对比。结果:在小鼠中,我们在AP/NTS中发现了可读检测到的Gfral mRNA,但在其他脑部位却没有。在外周组织中,我们在绝大多数被检查的组织中未能检测到任何gfral标记的细胞,即使存在,也是极其罕见的。人体组织的单细胞测序证实,在AP/NTS以外的一些部位,以极其稀疏的方式检测到表达gfral的细胞。重要的是,在使用的方法中,smFISH,遗传Gfral报告小鼠和scRNA-Seq,我们未能检测到Gfral标记的细胞。结论:通过高灵敏度和选择性技术,我们发现Gfral的表达绝大多数局限于脑干,并期望基于GDF15和Gfral的癌症恶病质治疗方法将特异性靶向AP/NTS细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GDNF family receptor alpha-like (GFRAL) expression is restricted to the caudal brainstem

Objective

Growth differentiation factor 15 (GDF15) acts on the receptor dimer of GDNF family receptor alpha-like (GFRAL) and Rearranged during transfection (RET). While Gfral-expressing cells are known to be present in the area postrema and nucleus of the solitary tract (AP/NTS) located in the brainstem, the presence of Gfral-expressing cells in other sites within the central nervous system and peripheral tissues is not been fully addressed. Our objective was to thoroughly investigate whether GFRAL is expressed in peripheral tissues and in brain sites different from the brainstem.

Methods

From Gfral:eGFP mice we collected tissue from 12 different tissues, including brain, and used single molecule in-situ hybridizations to identify cells within those tissues expressing Gfral. We then contrasted the results with human Gfral-expression by analyzing publicly available single-cell RNA sequencing data.

Results

In mice we found readably detectable Gfral mRNA within the AP/NTS but not within other brain sites. Within peripheral tissues, we failed to detect any Gfral-labelled cells in the vast majority of examined tissues and when present, were extremely rare. Single cell sequencing of human tissues confirmed GFRAL-expressing cells are detectable in some sites outside the AP/NTS in an extremely sparse manner. Importantly, across the utilized methodologies, smFISH, genetic Gfral reporter mice and scRNA-Seq, we failed to detect Gfral-labelled cells with all three.

Conclusions

Through highly sensitive and selective technologies we show Gfral expression is overwhelmingly restricted to the brainstem and expect that GDF15 and GFRAL-based therapies in development for cancer cachexia will specifically target AP/NTS cells.
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来源期刊
Molecular Metabolism
Molecular Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
14.50
自引率
2.50%
发文量
219
审稿时长
43 days
期刊介绍: Molecular Metabolism is a leading journal dedicated to sharing groundbreaking discoveries in the field of energy homeostasis and the underlying factors of metabolic disorders. These disorders include obesity, diabetes, cardiovascular disease, and cancer. Our journal focuses on publishing research driven by hypotheses and conducted to the highest standards, aiming to provide a mechanistic understanding of energy homeostasis-related behavior, physiology, and dysfunction. We promote interdisciplinary science, covering a broad range of approaches from molecules to humans throughout the lifespan. Our goal is to contribute to transformative research in metabolism, which has the potential to revolutionize the field. By enabling progress in the prognosis, prevention, and ultimately the cure of metabolic disorders and their long-term complications, our journal seeks to better the future of health and well-being.
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