Inflammation that occurs in the absence of microorganisms is called sterile inflammation. There are several classes of receptors that are responsible for detecting and triggering inflammatory responses. These are pattern recognition receptors (PRRs). The most famous of these are Toll-like receptors (TLRs), which are transmembrane proteins on the cell surface or in endosomes. One of them is TLR4. In the case of sterile inflammation 15-lipoxygenase (ALOX 15) has a role in the activation of TLR4. Extracellular vesicles (EV) are released from the cell in case of stress. EV have a membrane from lipids that can be substrate for peroxidation. ALOX 15 is the enzyme that is doing the peroxidation of phospholipid. The oxydised lipids can go and bind to the TLR4-MD-2 complex which leads to the activation of TLR4. Since it is not clear how the various mechanisms work, we wanted to make a cell line in which ALOX 15 would not express itself, which was the goal of this master's thesis. We decided to use the CRISPR/Cas9 system. We have designed and prepared the constructs according to the target sequence in the genome, introduced it into cells and we have made selection with puromycin. Genomic modification was verified by the T7E1 assay, five clones were selected for further work. We made a Western blot and immunodetection with antibodies to verify the reduced expression of ALOX 15. We have successfully made a cell line with a lower expression of ALOX 15, which allows further exploring the mechanism of activation along this pathway.
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