Hes Cecilia, Gui Lu Ting, Bay Alexandre, Alvarez Fernando, Katz Pierce, Paul Tanushree, Bozadjieva-Kramer Nadejda, Seeley Randy J, Piccirillo Ciriaco A, Sabatini Paul V
Research Institute of the McGill University Health Centre, McGill University Health Centre, 1001 boulevard de Decarie, Montreal, QC, H4A 3J1, Canada; Division of Experimental Medicine, Department of Medicine, McGill University, 1001 boulevard de Decarie, Montreal, QC, H4A 3J1, Canada.
Research Institute of the McGill University Health Centre, McGill University Health Centre, 1001 boulevard de Decarie, Montreal, QC, H4A 3J1, Canada; Integrated Program in Neuroscience, Department of Medicine, McGill University, Room 302 Irving Ludmer Building, 1033 Pine Ave. W. Montreal, QC, H3A 1A1, Canada.
Mol Metab. 2025 Jan;91:102070. doi: 10.1016/j.molmet.2024.102070. Epub 2024 Nov 26.
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.
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.
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.
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.
生长分化因子15(GDF15)作用于胶质细胞源性神经营养因子家族受体α样(GFRAL)和转染时重排(RET)的受体二聚体。虽然已知在脑干的最后区和孤束核(AP/NTS)中存在表达Gfral的细胞,但中枢神经系统和外周组织其他部位中表达Gfral的细胞的存在情况尚未得到充分研究。我们的目的是全面研究GFRAL是否在外周组织以及与脑干不同的脑区中表达。
我们从Gfral:eGFP小鼠收集了包括脑在内的12种不同组织的样本,并使用单分子原位杂交来识别这些组织中表达Gfral的细胞。然后,我们通过分析公开可用的单细胞RNA测序数据,将结果与人类Gfral表达情况进行对比。
在小鼠中,我们在AP/NTS内可检测到明显的Gfral mRNA,但在其他脑区未检测到。在外周组织中,我们在绝大多数检查的组织中未检测到任何Gfral标记的细胞,即使存在,也极为罕见。人类组织的单细胞测序证实,在AP/NTS以外的某些部位可以极其稀疏地检测到表达GFRAL的细胞。重要的是,通过所使用的三种方法,即单分子荧光原位杂交(smFISH)、基因Gfral报告基因小鼠和单细胞RNA测序(scRNA-Seq),我们均未检测到Gfral标记的细胞。
通过高灵敏度和高选择性的技术,我们发现Gfral的表达绝大多数局限于脑干,并预期正在开发的用于癌症恶病质的基于GDF15和GFRAL的疗法将特异性靶向AP/NTS细胞。