CSF1R 抑制剂 PLX3397 可消耗蒙古沙鼠的小胶质细胞,但不会消耗叙利亚仓鼠的小胶质细胞

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of pharmacological sciences Pub Date : 2024-03-23 DOI:10.1016/j.jphs.2024.03.003
Ren Y. Sato, Yumin Zhang , Koki T. Kotake , Hiraku Onishi, Shiho Ito, Hiroaki Norimoto, Zhiwen Zhou
{"title":"CSF1R 抑制剂 PLX3397 可消耗蒙古沙鼠的小胶质细胞,但不会消耗叙利亚仓鼠的小胶质细胞","authors":"Ren Y. Sato,&nbsp;Yumin Zhang ,&nbsp;Koki T. Kotake ,&nbsp;Hiraku Onishi,&nbsp;Shiho Ito,&nbsp;Hiroaki Norimoto,&nbsp;Zhiwen Zhou","doi":"10.1016/j.jphs.2024.03.003","DOIUrl":null,"url":null,"abstract":"<div><p>Microglia are the residential immune cells in the central nervous system. Their roles as innate immune cells and regulators of synaptic remodeling are critical to the development and the maintenance of the brain. Numerous studies have depleted microglia to elucidate their involvement in healthy and pathological conditions. PLX3397, a blocker of colony stimulating factor 1 receptor (CSF1R), is widely used to deplete mouse microglia due to its non-invasiveness and convenience. Recently, other small rodents, including Syrian hamsters (<em>Mesocricetus auratus</em>) and Mongolian gerbils (<em>Meriones unguiculatus</em>), have been recognized as valuable animal models for studying brain functions and diseases. However, whether microglia depletion via PLX3397 is feasible in these species remains unclear. Here, we administered PLX3397 orally via food pellets to hamsters and gerbils. PLX3397 successfully depleted gerbil microglia but had no effect on microglial density in hamsters. Comparative analysis of the CSF1R amino acid sequence in different species hints that amino acid substitutions in the juxtamembrane domain may potentially contribute to the inefficacy of PLX3397 in hamsters.</p></div>","PeriodicalId":16786,"journal":{"name":"Journal of pharmacological sciences","volume":"155 2","pages":"Pages 29-34"},"PeriodicalIF":3.0000,"publicationDate":"2024-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S134786132400029X/pdfft?md5=adbf8b5c2390572036d58aeb3338ba59&pid=1-s2.0-S134786132400029X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"CSF1R inhibitor PLX3397 depletes microglia in Mongolian gerbil Meriones unguiculatus, but not in syrian hamster Mesocricetus auratus\",\"authors\":\"Ren Y. Sato,&nbsp;Yumin Zhang ,&nbsp;Koki T. Kotake ,&nbsp;Hiraku Onishi,&nbsp;Shiho Ito,&nbsp;Hiroaki Norimoto,&nbsp;Zhiwen Zhou\",\"doi\":\"10.1016/j.jphs.2024.03.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Microglia are the residential immune cells in the central nervous system. Their roles as innate immune cells and regulators of synaptic remodeling are critical to the development and the maintenance of the brain. Numerous studies have depleted microglia to elucidate their involvement in healthy and pathological conditions. PLX3397, a blocker of colony stimulating factor 1 receptor (CSF1R), is widely used to deplete mouse microglia due to its non-invasiveness and convenience. Recently, other small rodents, including Syrian hamsters (<em>Mesocricetus auratus</em>) and Mongolian gerbils (<em>Meriones unguiculatus</em>), have been recognized as valuable animal models for studying brain functions and diseases. However, whether microglia depletion via PLX3397 is feasible in these species remains unclear. Here, we administered PLX3397 orally via food pellets to hamsters and gerbils. PLX3397 successfully depleted gerbil microglia but had no effect on microglial density in hamsters. Comparative analysis of the CSF1R amino acid sequence in different species hints that amino acid substitutions in the juxtamembrane domain may potentially contribute to the inefficacy of PLX3397 in hamsters.</p></div>\",\"PeriodicalId\":16786,\"journal\":{\"name\":\"Journal of pharmacological sciences\",\"volume\":\"155 2\",\"pages\":\"Pages 29-34\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-03-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S134786132400029X/pdfft?md5=adbf8b5c2390572036d58aeb3338ba59&pid=1-s2.0-S134786132400029X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pharmacological sciences\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S134786132400029X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmacological sciences","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S134786132400029X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

小胶质细胞是中枢神经系统中的居民免疫细胞。它们作为先天性免疫细胞和突触重塑的调节者,对大脑的发育和维护至关重要。大量研究已经耗尽了小胶质细胞,以阐明它们在健康和病理情况下的参与。PLX3397是集落刺激因子1受体(CSF1R)的阻断剂,因其非侵入性和方便性而被广泛用于消耗小鼠小胶质细胞。最近,包括叙利亚仓鼠(Mesocricetus auratus)和蒙古沙鼠(Meriones unguiculatus)在内的其他小型啮齿动物也被认为是研究大脑功能和疾病的重要动物模型。然而,通过 PLX3397 在这些物种中消耗小胶质细胞是否可行仍不清楚。在这里,我们通过食物颗粒给仓鼠和沙鼠口服 PLX3397。PLX3397 成功地消耗了沙鼠的小胶质细胞,但对仓鼠的小胶质细胞密度没有影响。对不同物种中CSF1R氨基酸序列的比较分析表明,并膜结构域的氨基酸替代可能是导致PLX3397对仓鼠无效的潜在原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
CSF1R inhibitor PLX3397 depletes microglia in Mongolian gerbil Meriones unguiculatus, but not in syrian hamster Mesocricetus auratus

Microglia are the residential immune cells in the central nervous system. Their roles as innate immune cells and regulators of synaptic remodeling are critical to the development and the maintenance of the brain. Numerous studies have depleted microglia to elucidate their involvement in healthy and pathological conditions. PLX3397, a blocker of colony stimulating factor 1 receptor (CSF1R), is widely used to deplete mouse microglia due to its non-invasiveness and convenience. Recently, other small rodents, including Syrian hamsters (Mesocricetus auratus) and Mongolian gerbils (Meriones unguiculatus), have been recognized as valuable animal models for studying brain functions and diseases. However, whether microglia depletion via PLX3397 is feasible in these species remains unclear. Here, we administered PLX3397 orally via food pellets to hamsters and gerbils. PLX3397 successfully depleted gerbil microglia but had no effect on microglial density in hamsters. Comparative analysis of the CSF1R amino acid sequence in different species hints that amino acid substitutions in the juxtamembrane domain may potentially contribute to the inefficacy of PLX3397 in hamsters.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.20
自引率
2.90%
发文量
104
审稿时长
31 days
期刊介绍: Journal of Pharmacological Sciences (JPS) is an international open access journal intended for the advancement of pharmacological sciences in the world. The Journal welcomes submissions in all fields of experimental and clinical pharmacology, including neuroscience, and biochemical, cellular, and molecular pharmacology for publication as Reviews, Full Papers or Short Communications. Short Communications are short research article intended to provide novel and exciting pharmacological findings. Manuscripts concerning descriptive case reports, pharmacokinetic and pharmacodynamic studies without pharmacological mechanism and dose-response determinations are not acceptable and will be rejected without peer review. The ethnopharmacological studies are also out of the scope of this journal. Furthermore, JPS does not publish work on the actions of biological extracts unknown chemical composition.
期刊最新文献
Rehmannioside A promotes the osteoblastic differentiation of MC3T3-E1 cells via the PI3K/AKT signaling pathway and inhibits glucocorticoid-induced bone loss in vivo Targeting TMEM16A ion channels suppresses airway hyperreactivity, inflammation, and remodeling in an experimental Guinea pig asthma model Glucosylceramide synthase inhibitor ameliorates chronic inflammatory pain TND1128, a 5-deazaflavin derivative with auto-redox ability, facilitates polarization of mitochondrial membrane potential (ΔΨm) and on-demand ATP synthesis in mice brain slices Analgesic effect of Keishinieppiittokajutsubu on low barometric pressure-induced pain response in arthritic model rats
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1