Effect of Jianpi Xiaoai Prescription on Activation of HFL1 into CAFs Induced by Exosomes in Colon Cancer
10.13422/j.cnki.syfjx.20201985
- VernacularTitle:健脾消癌方对结肠癌外泌体诱导HFL1活化成CAFs的影响
- Author:
Jia-qin LIU
1
;
Ji LUO
2
;
Yong-min LI
2
;
Xiao YANG
3
;
Xiao-ning TAN
2
;
Yan LUO
2
;
Yuan LYU
2
;
Yi-lan JIANG
2
Author Information
1. Graduate School， Hunan University of Chinese Medicine， Changsha 410208， China
2. Hunan Key Laboratory of Chinese Medicine Oncology， Innovative Platform of Antitumor Chinese Drugs， Hunan Academy of Traditional Chinese Medicine Affiliated Hospital， Changsha 410006， China
3. The First Hospital of Hunan University of Chinese Medicine， Changsha 410007， China
- Publication Type:Research Article
- Keywords:
colorectal cancer;
exosomes;
normal embryonic lung fibroblasts;
cancer associated fibroblasts;
α-smooth muscle actin （α-SMA）;
Jianpi Xiaoai prescription
- From:
Chinese Journal of Experimental Traditional Medical Formulae
2020;26(22):40-46
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To observe the effect of Jianpi Xiaoai prescription on the activation of normal human embryonic lung fibroblasts （HFL1） into tumor-associated fibroblasts （CAFs） induced by human colon cancer cells （HCT116） derived exosomes. Method:SD rats were gavaged with 13.1 g·kg-1 of Jianpi Xiaoai prescription to prepare drug-containing serum， and HCT116 cell exosomes-containing 10% exosomes-free serum and 20% Jianpi Xiaoai prescription drug serum were isolated by ultra-high speed centrifugation. The particle size distribution of exosomes were detected by Nanoparticle tracking analyzer （Zetaview）， and the exosomes' marker proteins apoptotic transfer gene 2 interaction protein X （Alix）， heat shock protein 70 （HSP70）， and tumor-susceptibility gene 101 （TSG101） were identified by Western blot， and the uptake of exosomes labeled with cell membrane staining kit （PKH67） by HFL1 was observed by fluorescence microscope. HFL1 cells were divided into six groups： the blank group， the transforming growth factor-β1 （TGF-β1） group， the TGF-β1 combined with HCT116 exosomes of 2 mg·L-1 group， the TGF-β1 combined with HCT116 exosomes of 4 mg·L-1 group， the TGF-β1 combined with Jianpi Xiaoai prescription exosomes of 2 mg·L-1 group， and the TGF-β1 combined with Jianpi Xiaoai prescription exosomes of 4 mg·L-1 group， and all groups were cultivated for 48 h. Western blot and Real-time fluorescence quantitative polymerase chain reaction （Real-time PCR） were used to determine the protein and mRNA expressions of α-smooth muscle actin （α-SMA）. Result:The particle size distribution detected by Zetaview was mainly between 50-100 nm， and the exosomes were verified based on the expressions of marker proteins Alix， HSP70 and TSG101. After co-incubation of HFL1 cells with exosomes， a large number of exosomes were absorbed by HFL1 cells under fluorescence microscope. Compared with the blank control group， the protein and mRNA expressions of α-SMA in the TGF-β1 group and TGF-β1 combined with HCT116 exosome groups were increased （P<0.01）. Compared with the TGF-β1 combined with HCT116 exosome groups， the protein and mRNA expressions of α-SMA were decreased in the TGF-β1 combined with Jianpi Xiaoai prescription exosome groups （P<0.01）. Conclusion:Human colon cancer cell exosomes combined with TGF-β1 can induce the activation of HFL1 into CAFs， and Jianpi Xiaoai prescription can reduce the activation of HFL1 by affecting the expressions of α-SMA， thus antagonizing the lung metastasis of colon cancer.
