Immune Surveillance by Myeloid-Derived Suppressor Cells in Liver Diseases

被引:2
作者
Sehgal, Rashi [1 ,2 ]
Kaur, Navkiran [2 ]
Ramakrishna, Gayatri [1 ]
Trehanpati, Nirupma [1 ]
机构
[1] Inst Liver & Biliary Sci, Dept Mol & Cellular Med, New Delhi, India
[2] Amity Univ, Amity Inst Biotechnol AIB, Noida, India
关键词
Myeloid-derived suppressor cells; Immunosuppression; Granulocytic myeloid-derived suppressor cells; Monocytic myeloid-derived suppressor cells; Sepsis; HEPATIC STELLATE CELLS; HEPATOCELLULAR-CARCINOMA; T-CELLS; SELF-RENEWAL; STEM-CELLS; EXPRESSION; CANCER; DIFFERENTIATION; ACCUMULATION; EXPANSION;
D O I
10.1159/000517459
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Myeloid-derived suppressor cells (MDSCs) are immunosuppressive in nature, originate in the bone marrow, and are mainly found in the blood, spleen, and liver. In fact, liver acts as an important organ for induction and accumulation of MDSCs, especially during infection, inflammation, and cancer. In humans and rodents, models of liver diseases revealed that MDSCs promote regeneration and drive the inflammatory processes, leading to hepatitis, fibrogenesis, and cirrhosis, ultimately resulting in hepatocellular carcinoma. Summary: This brief review is focused on the in-depth understanding of the key molecules involved in the expansion and regulation of MDSCs and their underlying immunosuppressive mechanisms in liver diseases. Key Message: Modulated MDSCs can be used for therapeutic purposes in inflammation, cancer, and sepsis.
引用
收藏
页码:301 / 312
页数:12
相关论文
共 113 条
[1]   Alcohol-induced miR-155 and HDAC11 inhibit negative regulators of the TLR4 pathway and lead to increased LPS responsiveness of Kupffer cells in alcoholic liver disease [J].
Bala, Shashi ;
Csak, Timea ;
Kodys, Karen ;
Catalano, Donna ;
Ambade, Aditya ;
Furi, Istvan ;
Lowe, Patrick ;
Cho, Yeonhee ;
Iracheta-Vellve, Arvin ;
Szabo, Gyongyi .
JOURNAL OF LEUKOCYTE BIOLOGY, 2017, 102 (02) :487-498
[2]   Histone deacetylase 4 promotes cholestatic liver injury in the absence of prohibitin-1 [J].
Barbier-Torres, Lucia ;
Beraza, Naiara ;
Fernandez-Tussy, Pablo ;
Lopitz-Otsoa, Fernando ;
Fernandez-Ramos, David ;
Zubiete-Franco, Imanol ;
Varela-Rey, Marta ;
Delgado, Teresa C. ;
Gutierrez, Virginia ;
Anguita, Juan ;
Pares, Albert ;
Banales, Jesus M. ;
Villa, Erica ;
Caballeria, Juan ;
Alvarez, Luis ;
Lu, Shelly C. ;
Mato, Jose M. ;
Martinez-Chantar, Maria Luz .
HEPATOLOGY, 2015, 62 (04) :1237-1248
[3]   Histone Deacetylase-1 (HDAC1) Is a Molecular Switch between Neuronal Survival and Death [J].
Bardai, Farah H. ;
Price, Valerie ;
Zaayman, Marcus ;
Wang, Lulu ;
D'Mello, Santosh R. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (42) :35444-35453
[4]   HDAC7 Is a Repressor of Myeloid Genes Whose Downregulation Is Required for Transdifferentiation of Pre-B Cells into Macrophages [J].
Barneda-Zahonero, Bruna ;
Roman-Gonzalez, Lidia ;
Collazo, Olga ;
Rafati, Haleh ;
Islam, Abul B. M. M. K. ;
Bussmann, Lars H. ;
di Tullio, Alessandro ;
De Andres, Luisa ;
Graf, Thomas ;
Lopez-Bigas, Nuria ;
Mahmoudi, Tokameh ;
Parra, Maribel .
PLOS GENETICS, 2013, 9 (05)
[5]   Histone deacetylase 11 as a key regulator of metabolism and obesity [J].
Bhaskara, Srividya .
EBIOMEDICINE, 2018, 35 :27-28
[6]   miR-146a is a significant brake on autoimmunity, myeloproliferation, and cancer in mice [J].
Boldin, Mark P. ;
Taganov, Konstantin D. ;
Rao, Dinesh S. ;
Yang, Lili ;
Zhao, Jimmy L. ;
Kalwani, Manorama ;
Garcia-Flores, Yvette ;
Luong, Mui ;
Devrekanli, Asli ;
Xu, Jessica ;
Sun, Guizhen ;
Tay, Jia ;
Linsley, Peter S. ;
Baltimore, David .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (06) :1189-1201
[7]   Mir-223 regulates the number and function of myeloid-derived suppressor cells in multiple sclerosis and experimental autoimmune encephalomyelitis [J].
Cantoni, Claudia ;
Cignarella, Francesca ;
Ghezzi, Laura ;
Mikesell, Bob ;
Bollman, Bryan ;
Berrien-Elliott, Melissa M. ;
Ireland, Aaron R. ;
Fehniger, Todd A. ;
Wu, Gregory F. ;
Piccio, Laura .
ACTA NEUROPATHOLOGICA, 2017, 133 (01) :61-77
[8]   Superantigen-induced CD4 T cell tolerance mediated by myeloid cells and IFN-γ [J].
Cauley, LS ;
Miller, EE ;
Yen, M ;
Swain, SL .
JOURNAL OF IMMUNOLOGY, 2000, 165 (11) :6056-6066
[9]   Role of histone deacetylase 9 in regulating adipogenic differentiation and high fat diet-induced metabolic disease [J].
Chatterjee, Tapan K. ;
Basford, Joshua E. ;
Yiew, Kan Hui ;
Stepp, David W. ;
Hui, David Y. ;
Weintraub, Neal L. .
ADIPOCYTE, 2014, 3 (04) :333-338
[10]   Role of HDAC9-FoxO1 Axis in the Transcriptional Program Associated with Hepatic Gluconeogenesis [J].
Chen, Jizheng ;
Zhang, Zhilei ;
Wang, Ning ;
Guo, Min ;
Chi, Xiumei ;
Pan, Yu ;
Jiang, Jing ;
Niu, Junqi ;
Ksimu, Sulaiman ;
Li, John Zhong ;
Chen, Xinwen ;
Wang, Qian .
SCIENTIFIC REPORTS, 2017, 7