Primary hepatocyte-derived liver precursor-like cell model, preparation method and application for hepatitis B virus infection
A technology of primary hepatocytes and cell models, applied in the field of cell transformation, HBV infection cell models in life sciences and medicine, can solve the problem of the single genetic background of human liver cancer cells, the inability to simulate the heterogeneity of HBV infected cells, and the The introduction of the source gene and the high cost of time and other problems have achieved the effect of broad clinical application prospects, avoiding tumorigenic risks, and chromosomal stability.
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Embodiment 1
[0056] Example 1. Obtainment of Hepatic Precursor-Like Cells HepLPCs and Identification of Related Characteristics
[0057] 1. Cell culture plate pre-coated
[0058] Use Matrigel matrix for coating, place the cryopreserved Matrigel matrix at 4°C overnight to make it liquid, dilute it with pre-cooled serum-free medium (such as DMEM) at 1:30, and add it to the culture well to cover the bottom surface. It can be used after placing it at 37°C for one hour.
[0059] 2. Obtaining HepLPCs from liver precursor-like cells
[0060] Take 2×10 4 cells / cm 2 Primary hepatocytes (PHCs) were inoculated in Matrigel-coated cell culture 6-well plates (purchased from Corning Company), and after adhering to the wall with WE medium containing 10% serum, the experimental group was replaced with improved hepatocytes The transformation and expansion medium (Transition and Expansion Medium, TEM) was cultured, and the control group was replaced with a commercially available hepatocyte growth medium ...
Embodiment 2
[0073] Example 2 Three-dimensional culture and liver maturation of HepLPCs
[0074] 1. Three-dimensional sphere culture of HepLPCs
[0075] Will 2×10 6 A proliferating HepLPCs was digested into single cells in Trypsin TrypLE Express, and then resuspended in a mixed medium, which was prepared by mixing equal volumes of TEM medium and HMM medium, and then inoculated in a low-adhesion medium Cells were cultured in 6-well plates (purchased from Corning); after the cells formed spheres, the medium was changed to Hepatic Maturation Medium (HMM), and differentiation was continued in HMM medium for 8-10 days After further maturation, they become three-dimensionally differentiated functional hepatocytes (3D-Hep LPCs-Hep). During the cultivation process, photographs were taken and recorded with an optical microscope at different time points.
[0076] Hepatocyte differentiation medium HMM includes two parts: basic support and small molecule supplement. The basic support is DMEM / F12 me...
Embodiment 3
[0084] Example 3 3D-HepLPCs-Hep Infection with HBV and Application Research
[0085] 1. Preparation of HBV-infected cell model
[0086] 3D-HepLPCs-Hep was co-cultured with hepatitis B patient serum or HepG2.2.15 cell culture supernatant concentrate in the liver supplemented with 1% DMSO and 4% polyethylene glycol 8000. In the cell transformation and proliferation medium; after 24 hours of infection, use the medium to wash three to four times, then change the medium every 24 hours, collect the supernatant and store it in a -80°C environment for later use.
[0087] 2. Detection of HBV-related indicators
[0088] Take the supernatants collected above on the 2nd day, the 4th day, the 6th day, the 8th day, and the 10th day respectively, and use ABI 7500 (purchased from Life Technologies Corporation) real-time fluorescent PCR method to detect the HBV-DNA virus in the supernatant For titer, Architect i2000SR was used to detect HBeAg and HBsAg secreted in the supernatant through arc...
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