Application of pou2f1 gene expression inhibitor in the preparation of medicaments for the treatment of tissue fibrosis
A technology of POU2F1, 1.POU2F1, applied in drug combination, disease diagnosis, respiratory system diseases, etc., can solve problems such as unsatisfactory application
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Embodiment 1
[0026] Example 1. In vitro experiments, using different matrix stiffness to simulate the impact of changes in extracellular matrix stiffness in different pathological conditions on the expression levels of transcription factor POU2F1 and myofibroblast markers fibronectin and αSMA in cardiac fibroblasts.
[0027] Isolation and culture of cardiac fibroblasts: Cardiac fibroblasts were obtained from 8- to 10-week-old male C57BL / 6 mice. The heart tissue from the atrial appendage was cut into pieces and then digested and separated using 0.1% type II collagenase (300U, 17101-015, Gibco, Carlsbad, CA, USA) in a water bath at 37°C. Afterwards, centrifuge at 1000 rpm for 5 minutes at room temperature, discard the supernatant, and wash the cell pellet with DMEM (12800-058, Gibco, Carlsbad, CA) containing 10% fetal bovine serum (15140-122, Gibco, Carlsbad, CA, USA). , USA) resuspended, then transferred to a 10cm petri dish, and cultured at 37°C and 5% carbon dioxide. This is the primary ...
Embodiment 2
[0037] Example 2. Detecting the POU2F1 protein level in the infarct area and remote area at different time points during heart tissue surgery in a mouse model of myocardial infarction.
[0038] 10-week-old male C57BL / 6 mice were used to establish the myocardial infarction model. The mice were randomly divided into myocardial infarction group and random control group. In the myocardial infarction group, left coronary artery stenosis was used to induce myocardial infarction. The control group underwent sham surgery. The operation was performed under gas anesthesia, and mice were gas anesthetized by inhalation of 2% isoflurane. In the experiment, the infarcted area and remote area of the heart tissue of the mice were collected at 1 day, 4 days, and 7 days after the operation.
[0039] We detected the protein level of the endogenous transcription factor POU2F1 in the heart tissue of the infarcted area and remote area of the mouse model of myocardial infarction by Western bl...
Embodiment 3
[0040] Example 3. Using chromatin immunoprecipitation experiments to determine that the transcription factor POU2F1 has the ability to bind to the promoters of its possible downstream genes.
[0041] Chromatin immunoprecipitation experiments: 1% formaldehyde was used to cross-link proteins and their associated DNA in live cardiac fibroblasts. Cell lysates were disrupted by sonication after cell fixation, and the size of DNA fragments was determined to be 500-600 bases by agarose gel electrophoresis. Antibody against POU2F1 (ab178869, abcam, Cambridge, MA, USA) and control rabbit monoclonal antibody IgG (ab172730, abcam, Cambridge, MA, USA) were used for immunobinding, and then A / G beads were added for immunoprecipitation. After the precipitate was centrifuged, it was washed with washing solutions of different salt concentrations, and then eluted and cross-linked, and then real-time quantitative PCR was used to detect the levels of IL1R2, CD69, and TGIF2 promoters.
[0042] Bo...
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