|Table of Contents|

Changes of the expression of CD45+,CD68+,CD163+ and CD11b+ immune cells in mouse lung tissue after surgical resection of tumor-bearing lymph node

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2021 02
Page:
181-184
Research Field:
Publishing date:

Info

Title:
Changes of the expression of CD45+,CD68+,CD163+ and CD11b+ immune cells in mouse lung tissue after surgical resection of tumor-bearing lymph node
Author(s):
JIANG Yourong1JIA Limin2HE Zhijin2ZHENG Jinhua2
1.Department of Oral Histopathology,the Affiliated Stomatological Hospital of Harbin Medical University,Heilongjiang Harbin 150001,China;2.Department of Anatomy,Harbin Medical University,Heilongjiang Harbin 150081,China.
Keywords:
surgerytumor-bearing lymph nodelungimmune cellsmicroenvironmentmouse
PACS:
R730.56
DOI:
10.3969/j.issn.1672-4992.2021.02.001
Abstract:
Objective:To investigate the effect of surgical resection of tumor-bearing lymph node on the expression of immune cells in mouse lung tissue.Methods:Mouse B16F10 melanoma cells were inoculated into mouse subiliac lymph node (SiLN).15 days later,tumor-bearing lymph node were surgically removed.All mice were divided into the surgical removal of SiLN group and the non-surgical removal group (control group).We used HE staining and Elastic-Masson staining to observe changes of general morphological structure and collagen fibers in mouse lung tissue,and applied immunohistochemistry to observe changes of CD45+,CD68+,CD163+,CD11b+ immune cells in mouse lung tissue.Results:Compared with the control group,pulmonary inflammatory cells infiltration in the surgical removal of lymph node group was significantly increased.The stromal collagen fibers around the blood vessels in lung tissues were sparse.The expression of CD45+ total inflammatory cells,CD68+ macrophages,CD163+ M2 macrophages and CD11b+ myeloid-derived suppressor cells (MDSCs) in mouse lung tissue were significantly increased(P<0.05).Conclusion:Surgical removal of tumor-bearing lymph node can promote the expression of CD163+ M2 macrophages and CD11b+ MDSC in mouse lung tissue,which is helpful to the formation of distant organ microenvironment that supports tumor cell colonization.

References:

[1]COX TR,GARTLAND A,ERLER JT.The pre-metastatic niche:Is metastasis random[J].Bonekey Rep,2012,1:80.
[2]CHEN Z,ZHANG P,XU Y,et al.Surgical stress and cancer progression:The twisted tango[J].Mol Cancer,2019,18(1):132.
[3]TOHME S,SIMMONS RL,TSUNG A.Surgery for cancer:A trigger for metastases[J].Cancer Res,2017,77(7):1548-1552.
[4]ZHANG Y,ZHANG N,HOFFMAN RM,et al.Surgically-induced multi-organ metastasis in an orthotopic syngeneic imageable model of 4T1 murine breast cancer[J].Anticancer Res,2015,35(9):4641-4646.
[5]ZHENG J,JIA L,MORI S,et al.Evaluation of metastatic niches in distant organs after surgical removal of tumor-bearing lymph nodes[J].BMC Cancer,2018,18(1):608.
[6]PEINADO H,ZHANG H,MATEI IR,et al.Pre-metastatic niches:Organ-specific homes for metastases[J].Nat Rev Cancer,2017,17(5):302-317.
[7]DOGLIONI G,PARIK S,FENDT SM.Interactions in the (pre)metastatic niche support metastasis formation[J].Front Oncol,2019,9:219.
[8]GUO Y,JI X,LIU J,et al.Effects of exosomes on pre-metastatic niche formation in tumors[J].Mol Cancer,2019,18(1):39.
[9]VERED M,SHNAIDERMAN-SHAPIRO A,SCHIBY G,et al.Markers of the pre-metastatic niche "knock on the door" of metastasis-free cervical lymph nodes in patients with oral cancer[J].Acta Histochem,2019,121(8):151447.
[10]MINAMI K,HIWATASHI K,UENO S,et al.Prognostic significance of CD68,CD163 and Folate receptor-beta positive macrophages in hepatocellular carcinoma[J].Exp Ther Med,2018,15(5):4465-4476.
[11]TROIANO G,CAPONIO VCA,ADIPIETRO I,et al.Prognostic significance of CD68(+) and CD163(+) tumor associated macrophages in head and neck squamous cell carcinoma:A systematic review and meta-analysis[J].Oral Oncol,2019,93:66-75.
[12]KERBEL RS.A decade of experience in developing preclinical models of advanced- or early-stage spontaneous metastasis to study antiangiogenic drugs,metronomic chemotherapy,and the tumor microenvironment[J].Cancer J,2015,21(4):274-283.
[13]LEE SY,JEONG EK,JU MK,et al.Induction of metastasis,cancer stem cell phenotype,and oncogenic metabolism in cancer cells by ionizing radiation[J].Mol Cancer,2017,16(1):10.
[14]BEHRENBRUCH C,SHEMBREY C,PAQUET-FIFIELD S,et al.Surgical stress response and promotion of metastasis in colorectal cancer:A complex and heterogeneous process[J].Clin Exp Metastasis,2018,35(4):333-345.
[15]HUANG X,LI Y,FU M,et al.Polarizing macrophages in vitro[J].Methods Mol Biol,2018,1784:119-126.
[16]TIAN J,RUI K,HONG Y,et al.Increased GITRL impairs the function of myeloid-derived suppressor cells and exacerbates primary sjogren syndrome[J].J Immunol,2019,202(6):1693-1703.
[17]TIAN J,RUI K,TANG X,et al.MicroRNA-9 regulates the differentiation and function of myeloid-derived suppressor cells via targeting Runx1[J].J Immunol,2015,195(3):1301-1311.
[18]VETSIKA EK,KOUKOS A,KOTSAKIS A.Myeloid-derived suppressor cells:Major figures that shape the immunosuppressive and angiogenic network in cancer[J].Cells,2019,8(12):1647.
[19]WU SY,CHIANG CS.Distinct role of CD11b(+)Ly6G(-)Ly6C(-) myeloid-derived cells on the progression of the primary tumor and therapy-associated recurrent brain tumor[J].Cells,2019,9(1):51.

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黑龙江省自然科学基金(编号:H2017015)
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