Increased expression of stress inducible protein 1 in glioma-associated microglia/macrophages

被引:63
|
作者
Carvalho da Fonseca, Anna Carolina [1 ]
Wang, Huaqing [2 ]
Fan, Haitao [2 ]
Chen, Xuebo [3 ]
Zhang, Ian [4 ]
Zhang, Leying [4 ]
Lima, Flavia Regina Souza [1 ]
Badie, Behnam [4 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Lab Morfogenese Celular, BR-21941 Rio De Janeiro, Brazil
[2] Shandong Univ, Prov Hosp, Dept Neurosurg, Jinan 250100, Peoples R China
[3] Jilin Univ, Hosp 2, Dept Gen Surg, Changchun 130023, Jilin Province, Peoples R China
[4] City Hope Beckman Res Inst, Dept Canc Immunotherapeut & Tumor Immunol, Div Neurosurg, Duarte, CA 91010 USA
关键词
Glioma; Glioma-associated microglia/macrophages; Stress-inducible protein 1; Glioma progression; Brain tumor microenvironment; PRION PROTEIN; CELLULAR PRION; ASTROCYTE DEVELOPMENT; OWN EXPRESSION; OVARIAN-CANCER; MICROGLIA; GROWTH; BRAIN; MICE; NEUROPROTECTION;
D O I
10.1016/j.jneuroim.2014.06.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Factors released by glioma-associated microglia/macrophages (GAMs) play an important role in the growth and infiltration of tumors. We have previously demonstrated that the co-chaperone stress-inducible protein 1 (STI1) secreted by microglia promotes proliferation and migration of human glioblastoma (GBM) cell lines in vitro. In the present study, in order to investigate the role of STI1 in a physiological context, we used a glioma model to evaluate STI1 expression in vivo. Here, we demonstrate that STI1 expression in both the tumor and in the infiltrating GAMs and lymphocytes significantly increased with tumor progression. Interestingly, high expression of STI1 was observed in macrophages and lymphocytes that infiltrated brain tumors, whereas STI1 expression in the circulating blood monocytes and lymphocytes remained unchanged. Our results correlate, for the first time, the expression of STI1 and glioma progression, and suggest that STI1 expression in GAMs and infiltrating lymphocytes is modulated by the brain tumor microenvironment (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 77
页数:7
相关论文
共 50 条
  • [21] Innate and adaptive immune responses by glioma-associated microglia
    Crane, Courtney
    Kabongo, Tshilumna
    Murray, Joseph
    Parsa, Andrew
    NEURO-ONCOLOGY, 2007, 9 (04) : 506 - 506
  • [22] Ablation Of Neuropilin 1 in Glioma-Associated Macrophages Slows Tumor Progression
    Miyauchi, Jeremy Tetsuo
    Chen, Danling
    Nissen, Jillian
    Shroyer, Kenneth
    Selwood, David
    Tsirka, Stella
    FASEB JOURNAL, 2016, 30
  • [23] CSF1 Overexpression Promotes High-Grade Glioma Formation without Impacting the Polarization Status of Glioma-Associated Microglia and Macrophages
    De, Ishani
    Steffen, Megan D.
    Clark, Paul A.
    Patros, Clayton J.
    Sokn, Emily
    Bishop, Stephanie M.
    Litscher, Suzanne
    Maklakova, Vilena I.
    Kuo, John S.
    Rodriguez, Fausto J.
    Collier, Lara S.
    CANCER RESEARCH, 2016, 76 (09) : 2552 - 2560
  • [24] Regulation of IL-10 expression by upstream stimulating factor (USF-1) in glioma-associated microglia
    Zhang, Leying
    Van Handel, Michelle
    Schartner, Jill M.
    Hagar, Aaron
    Allen, Grant
    Curet, Madorie
    Badie, Behnam
    JOURNAL OF NEUROIMMUNOLOGY, 2007, 184 (1-2) : 188 - 197
  • [25] Origin, activation, and targeted therapy of glioma-associated macrophages
    Xu, Can
    Xiao, Menglin
    Li, Xiang
    Xin, Lei
    Song, Jia
    Zhan, Qi
    Wang, Changsheng
    Zhang, Qisong
    Yuan, Xiaoye
    Tan, Yanli
    Fang, Chuan
    FRONTIERS IN IMMUNOLOGY, 2022, 13
  • [26] Glioma-associated microglia and macrophages/monocytes display distinct electrophysiological properties and do not communicate via gap junctions
    Richter, Nadine
    Wendt, Stefan
    Georgieva, Petya B.
    Hambardzumyan, Dolores
    Nolte, Christiane
    Kettenmann, Helmut
    NEUROSCIENCE LETTERS, 2014, 583 : 130 - 135
  • [27] Glioma-Associated Microglia/Macrophages Display an Expression Profile Different from M1 and M2 Polarization and Highly Express Gpnmb and Spp1
    Szulzewsky, Frank
    Pelz, Andreas
    Feng, Xi
    Synowitz, Michael
    Markovic, Darko
    Langmann, Thomas
    Holtman, Inge R.
    Wang, Xi
    Eggen, Bart J. L.
    Boddeke, Hendrikus W. G. M.
    Hambardzumyan, Dolores
    Wolf, Susanne A.
    Kettenmann, Helmut
    PLOS ONE, 2015, 10 (02):
  • [28] Combination of p38 MAPK inhibitor with PD-L1 antibody effectively prolongs survivals of temozolomide-resistant glioma-bearing mice via reduction of infiltrating glioma-associated macrophages and PD-L1 expression on resident glioma-associated microglia
    Weiqi Dang
    Jingfang Xiao
    Qinghua Ma
    Jingya Miao
    Mianfu Cao
    Lu Chen
    Yu Shi
    Xiaohong Yao
    Shichang Yu
    Xindong Liu
    Youhong Cui
    Xia Zhang
    Xiuwu Bian
    Brain Tumor Pathology, 2021, 38 : 189 - 200
  • [29] Combination of p38 MAPK inhibitor with PD-L1 antibody effectively prolongs survivals of temozolomide-resistant glioma-bearing mice via reduction of infiltrating glioma-associated macrophages and PD-L1 expression on resident glioma-associated microglia
    Dang, Weiqi
    Xiao, Jingfang
    Ma, Qinghua
    Miao, Jingya
    Cao, Mianfu
    Chen, Lu
    Shi, Yu
    Yao, Xiaohong
    Yu, Shichang
    Liu, Xindong
    Cui, Youhong
    Zhang, Xia
    Bian, Xiuwu
    BRAIN TUMOR PATHOLOGY, 2021, 38 (03) : 189 - 200
  • [30] Flow cytometry and in vitro analysis of human glioma-associated macrophages
    Parney, Ian F.
    Waldron, James S.
    Parsa, Andrew T.
    JOURNAL OF NEUROSURGERY, 2009, 110 (03) : 572 - 582