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Gd-metallofullerenol nanoparticles cause intracellular accumulation of pdgfr-alpha and morphology alteration of fibroblasts
Tang, Jinglong1,2,5; Guo, Mengyu1,2,6; Wang, Peng3,4; Liu, Jing1,2; Xiao, Yating1,2,6; Cheng, Wenting5; Gao, Jinling5; Hu, Wenquan3,4; Miao, Qing Robert1,2,3,4
刊名Nanoscale
2019-03-21
卷号11期号:11页码:4743-4750
ISSN号2040-3364
DOI10.1039/c8nr08667b
通讯作者Miao, qing robert(miaoq@nanoctr.cn)
英文摘要Gadolinium-metallofullerenols (gd@c-82(oh)(22)) are a promising agent for cancer therapy and have shown beneficial effects in regulating the tumor microenvironment with low toxicity. however, the underlying mechanism by which gd@c-82(oh)(22) interacts with fibroblasts remains unclear. in order to explore the critical role that activated fibroblasts play in tumorigenesis and fibrosis, we investigated the regulatory effect of gd@c-82(oh)(22) in fibroblast activation and oncogenic transformation, and found that the pdgfr-alpha is an essential molecule in modulating the morphology and functional changes in fibroblasts after gd@c-82(oh)(22) treatment. apart from increasing the pdgfr-alpha protein level, gd@c-82(oh)(22) nanoparticles also significantly increased the protein level of rab5, which is required for regulating pdgfr-alpha endosomal recycling. the rab5-mediated recycling of pdgfr-alpha maybe attributed to the gd@c-82(oh)(22) regulated inhibition of fibroblast activation. overall, our work demonstrated that gd@c-82(oh)(22)( )nanoparticles can attenuate the pdgf-stimulated phosphorylation of pdgfr-alpha in fibroblasts and suppress the fibroblast activation by interrupting endosomal recycling. these findings may be contributed to the collagen accumulation for encaging cancer.
资助项目National Natural Science Foundation of China[31571027] ; National Natural Science Foundation of China[81872651] ; Ministry of Science and Technology of China (National Basic Research Program)[2016YFA0201600] ; Division of Pediatric Surgery, Medical College of Wisconsin (MCW) ; Division of Pediatric Pathology, Medical College of Wisconsin (MCW) ; Advancing a Healthier Wisconsin endowment ; Children's Hospital of Wisconsin Research Institute Pilot Innovative Research Grant
WOS关键词PANCREATIC-CANCER METASTASIS ; GROWTH-FACTOR PDGF ; RECEPTOR-ALPHA ; STEM-CELLS ; BETA ; INHIBIT
WOS研究方向Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics
WOS类目Chemistry, Multidisciplinary ; Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary ; Physics, Applied
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000462669600049
资助机构National Natural Science Foundation of China ; Ministry of Science and Technology of China (National Basic Research Program) ; Division of Pediatric Surgery, Medical College of Wisconsin (MCW) ; Division of Pediatric Pathology, Medical College of Wisconsin (MCW) ; Advancing a Healthier Wisconsin endowment ; Children's Hospital of Wisconsin Research Institute Pilot Innovative Research Grant
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/2160633
专题高能物理研究所
通讯作者Miao, Qing Robert
作者单位1.Natl Ctr Nanosci & Technol China, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
2.Natl Ctr Nanosci & Technol China, CAS Ctr Excellence Nanosci, Beijing 100190, Peoples R China
3.Med Coll Wisconsin, Dept Surg, Childrens Res Inst, 8700 W Wisconsin Ave, Milwaukee, WI 53226 USA
4.Med Coll Wisconsin, Dept Pathol, Childrens Res Inst, Milwaukee, WI 53226 USA
5.Qingdao Univ, Sch Publ Hlth, Qingdao 226021, Shandong, Peoples R China
6.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Tang, Jinglong,Guo, Mengyu,Wang, Peng,et al. Gd-metallofullerenol nanoparticles cause intracellular accumulation of pdgfr-alpha and morphology alteration of fibroblasts[J]. Nanoscale,2019,11(11):4743-4750.
APA Tang, Jinglong.,Guo, Mengyu.,Wang, Peng.,Liu, Jing.,Xiao, Yating.,...&Miao, Qing Robert.(2019).Gd-metallofullerenol nanoparticles cause intracellular accumulation of pdgfr-alpha and morphology alteration of fibroblasts.Nanoscale,11(11),4743-4750.
MLA Tang, Jinglong,et al."Gd-metallofullerenol nanoparticles cause intracellular accumulation of pdgfr-alpha and morphology alteration of fibroblasts".Nanoscale 11.11(2019):4743-4750.
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