Immunohistochemistry Staining for Tumor-associated Macrophage Polarization in Murine Subcutaneous Colon Tumor Allografts

BIO-PROTOCOL ◽  
2018 ◽  
Vol 8 (23) ◽  
Author(s):  
Gage Greening ◽  
Shelby Bess ◽  
Timothy Muldoon
Autophagy ◽  
2020 ◽  
Vol 16 (11) ◽  
pp. 2069-2083 ◽  
Author(s):  
Enyong Dai ◽  
Leng Han ◽  
Jiao Liu ◽  
Yangchun Xie ◽  
Guido Kroemer ◽  
...  

Aging ◽  
2020 ◽  
Author(s):  
Xin Yuan ◽  
Ya Li ◽  
An Zhi Zhang ◽  
Chen Hao Jiang ◽  
Fan Ping Li ◽  
...  

Author(s):  
Jinying Yang ◽  
Yumian Lai ◽  
Juanhua Chen ◽  
Baohua Lin ◽  
Bei Zhou ◽  
...  

Abstract To test the hypothesis that changes in alpha-7 nicotinic acetylcholine receptor (α7nAChR) expression on macrophages and macrophage polarization participate in cervical remodeling during normal pregnancy, pregnant rats from gestational days (GDs) 14, 16, 18, 20, and 22 were used in the present study. The expression of α7nAChR on macrophages and the numbers of M1 and M2 macrophages were detected by double immunofluorescence staining. The levels of α7nAChR and collagens were detected by western blotting. M1 markers (inducible nitric oxide synthase and inflammatory cytokines) and M2 markers (arginase 1, anti-inflammatory cytokines) were detected to evaluate the macrophage polarization state by immunohistochemistry staining, western blotting, and the enzyme-linked immunosorbent assay. Matrix metalloproteinase 9 (MMP-9) expression was determined by immunohistochemistry staining and western blotting. We found that the α7nAChR expression on macrophages significantly decreased on GD22 compared to GDs 14, 16, 18, and 20. There was an increased number of M1 macrophages and decreased number of M2 macrophages in late pregnancy. The expression of M1 macrophage biomarkers was much higher on GDs 20 and 22 than on GDs 14, 16, and 18, but expression of M2 biomarkers decreased on GDs 20 and 22 compared to GDs 14, 16, and 18. MMP-9 expression was higher on GD22 than on GDs 14, 16, 18, and 20, and collagen expression significantly decreased on GDs 18, 20, and 22 compared to GD14. Our results indicated that the decreased expression of α7nAChR and increased number of M1 macrophages are associated with cervical remodeling.


Cells ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 174 ◽  
Author(s):  
Giulia Gionfriddo ◽  
Pierluigi Plastina ◽  
Giuseppina Augimeri ◽  
Stefania Catalano ◽  
Cinzia Giordano ◽  
...  

Activation of peroxisome proliferator-activated receptor gamma (PPARγ) elicits anti-proliferative effects on different tumor cells, including those derived from breast cancer. PPARγ is also expressed in several cells of the breast tumor microenvironment, among which tumor associated macrophages (TAMs) play a pivotal role in tumor progression and metastasis. We explored the ability of synthetic and natural PPARγ ligands to modulate TAM polarization. The ligands included rosiglitazone (BRL-49653), and two docosahexaenoic acid (DHA) conjugates, N-docosahexaenoyl ethanolamine (DHEA) and N-docosahexaenoyl serotonin (DHA-5-HT). Human THP-1 monocytic cells were differentiated into M0, M1 and M2 macrophages that were characterized by qRT-PCR, ELISA and western blotting. A TAM-like phenotypic state was generated by adding two different breast cancer cell conditioned media (BCC-CM) to the cultures. Macrophages exposed to BCC-CM concomitantly exhibited M1 and M2 phenotypes. Interestingly, rosiglitazone, DHEA and DHA-5-HT attenuated cytokine secretion by TAMs, and this effect was reversed by the PPARγ antagonist GW9662. Given the key role played by PPARγ in the crosstalk between cancer cells and TAMs in tumor progression, its activation via endogenous or synthetic ligands may lead to novel strategies that target both epithelial neoplastic cells and the tumor microenvironment.


Aging ◽  
2020 ◽  
Author(s):  
Lijia Zhong ◽  
Yuanyuan Zhang ◽  
Mengyao Li ◽  
Yinjing Song ◽  
Danhui Liu ◽  
...  

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