• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

GFRAL 在小鼠的大脑和外周组织中广泛分布。

GFRAL Is Widely Distributed in the Brain and Peripheral Tissues of Mice.

机构信息

Rudolf Boehm Institute of Pharmacology and Toxicology, Faculty of Medicine, University of Leipzig, D-04103 Leipzig, Germany.

School of Acupuncture and Tuina, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China.

出版信息

Nutrients. 2024 Mar 4;16(5):734. doi: 10.3390/nu16050734.

DOI:10.3390/nu16050734
PMID:38474863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10933958/
Abstract

In 2017, four independent publications described the glial cell-derived neurotrophic factor (GDNF) receptor alpha-like (GFRAL) as receptor for the growth differentiation factor 15 (GDF15, also MIC-1, NAG-1) with an expression exclusively in the mice brainstem area postrema (AP) and nucleus tractus solitarii (NTS) where it mediates effects of GDF15 on reduction of food intake and body weight. GDF15 is a cell stress cytokine with a widespread expression and pleiotropic effects, which both seem to be in contrast to the reported highly specialized localization of its receptor. This discrepancy prompts us to re-evaluate the expression pattern of GFRAL in the brain and peripheral tissues of mice. In this detailed immunohistochemical study, we provide evidence for a more widespread distribution of this receptor. Apart from the AP/NTS region, GFRAL-immunoreactivity was found in the prefrontal cortex, hippocampus, nucleus arcuatus and peripheral tissues including liver, small intestine, fat, kidney and muscle tissues. This widespread receptor expression, not taken into consideration so far, may explain the multiple effects of GDF-15 that are not yet assigned to GFRAL. Furthermore, our results could be relevant for the development of novel pharmacological therapies for physical and mental disorders related to body image and food intake, such as eating disorders, cachexia and obesity.

摘要

2017 年,有四项独立的出版物将胶质细胞衍生的神经营养因子 (GDNF) 受体α样 (GFRAL) 描述为生长分化因子 15 (GDF15,也称为 MIC-1、NAG-1) 的受体,其在表达上仅存在于小鼠的脑干后区 (AP) 和孤束核 (NTS) 中,在那里它介导 GDF15 对减少食物摄入和体重的作用。GDF15 是一种细胞应激细胞因子,具有广泛的表达和多效性效应,这似乎与报道的其受体高度特化的定位相矛盾。这种差异促使我们重新评估 GFRAL 在小鼠大脑和外周组织中的表达模式。在这项详细的免疫组织化学研究中,我们提供了证据表明该受体的分布更为广泛。除了 AP/NTS 区域,GFRAL 免疫反应性还存在于前额叶皮层、海马体、弓状核和外周组织,包括肝脏、小肠、脂肪、肾脏和肌肉组织。到目前为止,这种广泛的受体表达可能解释了 GDF-15 的多种作用,这些作用尚未被分配给 GFRAL。此外,我们的研究结果可能与与身体形象和食物摄入相关的身心障碍的新型药理学治疗的发展有关,例如饮食失调、恶病质和肥胖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/c140c83ba5fa/nutrients-16-00734-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/4de6c4f92e47/nutrients-16-00734-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/5c5e7ca50d4d/nutrients-16-00734-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/02381daa4f32/nutrients-16-00734-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/c140c83ba5fa/nutrients-16-00734-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/4de6c4f92e47/nutrients-16-00734-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/5c5e7ca50d4d/nutrients-16-00734-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/02381daa4f32/nutrients-16-00734-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1871/10933958/c140c83ba5fa/nutrients-16-00734-g004.jpg

相似文献

1
GFRAL Is Widely Distributed in the Brain and Peripheral Tissues of Mice.GFRAL 在小鼠的大脑和外周组织中广泛分布。
Nutrients. 2024 Mar 4;16(5):734. doi: 10.3390/nu16050734.
2
GDF15 mediates adiposity resistance through actions on GFRAL neurons in the hindbrain AP/NTS.GDF15 通过作用于后脑 AP/NTS 中的 GFRAL 神经元来介导肥胖抵抗。
Int J Obes (Lond). 2019 Dec;43(12):2370-2380. doi: 10.1038/s41366-019-0365-5. Epub 2019 May 31.
3
GDF15 acts synergistically with liraglutide but is not necessary for the weight loss induced by bariatric surgery in mice.GDF15 与利拉鲁肽协同作用,但不是减肥手术诱导小鼠体重减轻所必需的。
Mol Metab. 2019 Mar;21:13-21. doi: 10.1016/j.molmet.2019.01.003. Epub 2019 Jan 14.
4
The metabolic effects of GDF15 are mediated by the orphan receptor GFRAL.GDF15 的代谢作用是由孤儿受体 GFRAL 介导的。
Nat Med. 2017 Oct;23(10):1215-1219. doi: 10.1038/nm.4393. Epub 2017 Aug 28.
5
The MIC-1/GDF15-GFRAL Pathway in Energy Homeostasis: Implications for Obesity, Cachexia, and Other Associated Diseases.MIC-1/GDF15-GFRAL 通路与能量稳态:肥胖症、恶病质及其他相关疾病的影响。
Cell Metab. 2018 Sep 4;28(3):353-368. doi: 10.1016/j.cmet.2018.07.018.
6
Targeting Obesity and Cachexia: Identification of the GFRAL Receptor-MIC-1/GDF15 Pathway.靶向肥胖与恶病质:GFRAL 受体-MIC-1/GDF15 通路的鉴定。
Trends Mol Med. 2017 Dec;23(12):1065-1067. doi: 10.1016/j.molmed.2017.10.005. Epub 2017 Nov 9.
7
GFRAL is the receptor for GDF15 and the ligand promotes weight loss in mice and nonhuman primates.GFRAL 是 GDF15 的受体,该配体可促进小鼠和非人灵长类动物的体重减轻。
Nat Med. 2017 Oct;23(10):1150-1157. doi: 10.1038/nm.4392. Epub 2017 Aug 28.
8
Non-homeostatic body weight regulation through a brainstem-restricted receptor for GDF15.通过脑干限制性 GDF15 受体实现非稳态体重调节。
Nature. 2017 Oct 12;550(7675):255-259. doi: 10.1038/nature24042. Epub 2017 Sep 27.
9
GFRAL is the receptor for GDF15 and is required for the anti-obesity effects of the ligand.GFRAL 是 GDF15 的受体,是配体发挥抗肥胖作用所必需的。
Nat Med. 2017 Oct;23(10):1158-1166. doi: 10.1038/nm.4394. Epub 2017 Aug 28.
10
GDNF family receptor alpha-like antagonist antibody alleviates chemotherapy-induced cachexia in melanoma-bearing mice.GDNF 家族受体 α 样拮抗剂抗体可减轻荷黑色素瘤小鼠的化疗性恶病质。
J Cachexia Sarcopenia Muscle. 2023 Jun;14(3):1441-1453. doi: 10.1002/jcsm.13219. Epub 2023 Apr 5.

引用本文的文献

1
GDF15 promotes osteogenic differentiation of human dental pulp stem cells by activating the TGF-β/SMAD signaling pathway.生长分化因子15通过激活转化生长因子-β/信号转导和转录激活因子信号通路促进人牙髓干细胞的成骨分化。
J Tissue Eng. 2025 Jul 28;16:20417314251357752. doi: 10.1177/20417314251357752. eCollection 2025 Jan-Dec.
2
Growth Differentiation Factor 15 Induces Gastric Fundus Contraction Involving Cholinergic Excitation: Morphofunctional Evidence in Rodent Models.生长分化因子15通过胆碱能兴奋诱导胃底收缩:啮齿动物模型中的形态功能证据
J Cell Mol Med. 2025 Jun;29(11):e70629. doi: 10.1111/jcmm.70629.
3
Repression of oxidative phosphorylation by NR2F2, MTERF3 and GDF15 in human skin under high-glucose stress.

本文引用的文献

1
Genetic variants identified in novel candidate genes for anorexia nervosa and analysis of molecular pathways for diagnostic applications.新型神经性厌食症候选基因中的遗传变异及其在诊断应用中的分子途径分析。
Eur Rev Med Pharmacol Sci. 2023 Dec;27(6 Suppl):77-88. doi: 10.26355/eurrev_202312_34692.
2
GDF15 promotes weight loss by enhancing energy expenditure in muscle.GDF15 通过增强肌肉能量消耗促进体重减轻。
Nature. 2023 Jul;619(7968):143-150. doi: 10.1038/s41586-023-06249-4. Epub 2023 Jun 28.
3
Growth differentiation factor 15 (GDF-15) in endocrinology.
在高糖应激下,NR2F2、MTERF3和GDF15对人皮肤中氧化磷酸化的抑制作用。
Redox Biol. 2025 May;82:103613. doi: 10.1016/j.redox.2025.103613. Epub 2025 Mar 27.
4
Growth Differentiation Factor-15 Knockout Mice Are Protected from Neonatal Hypoxic-Ischemic Injury in a Sex-Dependent Manner.生长分化因子-15基因敲除小鼠以性别依赖的方式免受新生儿缺氧缺血性损伤。
Dev Neurosci. 2025 Feb 10:1-10. doi: 10.1159/000544063.
5
GDF15 Analogues Acting as GFRAL Ligands.作为GFRAL配体的GDF15类似物。
ChemMedChem. 2025 May 5;20(9):e202400961. doi: 10.1002/cmdc.202400961. Epub 2025 Feb 17.
6
Diversity of Microglia-Derived Molecules with Neurotrophic Properties That Support Neurons in the Central Nervous System and Other Tissues.具有神经营养特性的小胶质细胞衍生分子的多样性,这些分子在中枢神经系统和其他组织中支持神经元。
Molecules. 2024 Nov 22;29(23):5525. doi: 10.3390/molecules29235525.
7
GDF15/MIC-1: a stress-induced immunosuppressive factor which promotes the aging process.生长分化因子15/巨噬细胞抑制性细胞因子1:一种应激诱导的免疫抑制因子,可促进衰老进程。
Biogerontology. 2024 Dec 6;26(1):19. doi: 10.1007/s10522-024-10164-0.
8
GDNF family receptor alpha-like (GFRAL) expression is restricted to the caudal brainstem.胶质细胞源性神经营养因子家族受体α样蛋白(GFRAL)的表达局限于脑干尾部。
Mol Metab. 2025 Jan;91:102070. doi: 10.1016/j.molmet.2024.102070. Epub 2024 Nov 26.
9
GDF15 associates with, but is not responsible for, exercise-induced increases in corticosterone and indices of lipid utilization in mice.GDF15 与运动引起的皮质酮增加和小鼠脂质利用指标相关,但不负责这些变化。
J Appl Physiol (1985). 2024 Dec 1;137(6):1512-1523. doi: 10.1152/japplphysiol.00519.2024. Epub 2024 Oct 31.
10
Hepatocyte-specific GDF15 overexpression improves high-fat diet-induced obesity and hepatic steatosis in mice via hepatic FGF21 induction.肝细胞特异性 GDF15 过表达通过诱导肝 FGF21 改善高脂肪饮食诱导的肥胖和肝脂肪变性。
Sci Rep. 2024 Oct 14;14(1):23993. doi: 10.1038/s41598-024-75107-8.
生长分化因子 15(GDF-15)在内分泌学中的作用。
Endocrine. 2023 Sep;81(3):419-431. doi: 10.1007/s12020-023-03377-9. Epub 2023 May 2.
4
The expression pattern of GDF15 in human brain changes during aging and in Alzheimer's disease.GDF15在人脑中的表达模式在衰老过程和阿尔茨海默病中会发生变化。
Front Aging Neurosci. 2023 Jan 9;14:1058665. doi: 10.3389/fnagi.2022.1058665. eCollection 2022.
5
GDF15 is an exercise-induced hepatokine regulated by glucagon and insulin in humans.GDF15 是一种运动诱导的肝激素,在人类中受胰高血糖素和胰岛素调节。
Front Endocrinol (Lausanne). 2022 Dec 5;13:1037948. doi: 10.3389/fendo.2022.1037948. eCollection 2022.
6
Adipokines, Hepatokines and Myokines: Focus on Their Role and Molecular Mechanisms in Adipose Tissue Inflammation.脂联素、肝激素和肌激素:聚焦它们在脂肪组织炎症中的作用和分子机制。
Front Endocrinol (Lausanne). 2022 Jul 14;13:873699. doi: 10.3389/fendo.2022.873699. eCollection 2022.
7
The Role of GDF15 as a Myomitokine.生长分化因子 15 作为肌因子的作用。
Cells. 2021 Nov 3;10(11):2990. doi: 10.3390/cells10112990.
8
GDF15: emerging biology and therapeutic applications for obesity and cardiometabolic disease.生长分化因子15:肥胖和心血管代谢疾病的新兴生物学及治疗应用
Nat Rev Endocrinol. 2021 Oct;17(10):592-607. doi: 10.1038/s41574-021-00529-7. Epub 2021 Aug 11.
9
Arcuate nucleus, median eminence, and hypophysial pars tuberalis.弓状核、正中隆起和垂体结节部。
Handb Clin Neurol. 2021;180:227-251. doi: 10.1016/B978-0-12-820107-7.00015-X.
10
Expression of the Body-Weight Signaling Players: GDF15, GFRAL and RET and their clinical relevance in Gastric Cancer.体重信号相关因子:生长分化因子15(GDF15)、生长分化因子15受体(GFRAL)和受体酪氨酸激酶(RET)的表达及其在胃癌中的临床相关性
J Cancer. 2021 Jun 4;12(15):4698-4709. doi: 10.7150/jca.55511. eCollection 2021.