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Introduction: One of the most important issues raised by the outbreak of the COVID-19 Pandemic is its impact on political philosophy. The pandemic opened an antagonistic space regarding the existing components of political philosophy and challenge them. In fact, the COVID-19 Pandemic provided a critical platform for questioning the established norms and prompted discussions on the necessity of rethinking and re-evaluating them. The purpose of this article is to answer the fundamental question of how the COVID-19 Pandemic has created an antagonistic space for the elements of modern political philosophy. Methods: The method used in this article is the critical method. Critical theory seeks to develop and expand the understanding and awareness that penetrates beyond surface appearances to the depth of reality in order to increase the power of correct recognition of people, especially the powerless or subjugated classes. The critical aspect of this article allows the author to present the relations emerging from the COVID-19 in human societies as unacceptable and replaceable. This method helps to identify and challenge social and cultural issues in society and is effective in improving and developing human relations during pandemics. The information gathering method is both library-based and internet-based. Results and discussion: Among the most important challenges that COVID-19 has posed to the new political philosophy are the questioning of concepts such as rationalism, humanism and individualism, which have been temporarily challenged by the pandemic. It can be said that this virus embodies the friend/enemy distinction and Schmitt's narrative of the political in the context of the COVID-19 situation presented itself in the form of a confrontation between the coronavirus and humanity. Humanity, once perceived as dominant over nature and the world, has been rendered weak and powerless by the virus. Furthermore, rationalism and scientism of philosophy of modernity which held that humanity, through these principles, could intervene in all matters and solve its problems independently of the external world, have also been brought into conflict by the pandemic. COVID-19 has highlighted the weaknesses and limitations of human reason. Categories such as artificial intelligence have easily been able to fit themselves in the clothes of the enemy of human reason, and as Farid Zakaria points out, during the pandemic, we have come to worship artificial intelligence like a God. Therefore, despite the abundant services of science and rationality to mankind, COVID-19 has reminded us that they still have undeniable limitations and cannot be the sole solutions to human problems. Conclusion: The danger of COVID-19 highlights the risks of technological manipulation of human and natural resources, using calculative and computational reasoning as a tool for the economic benefit and overall utility of dominant powers. Environmental destruction is an act of violence against nature, leading to humanity's self-destruction through the creation of pandemics that challenge human life. Therefore, attempts to prevent or resolve the riddle of pandemics require something more than the calculative and computational knowledge of modernity. [ABSTRACT FROM AUTHOR]

Background: Iranian Lizard Leishmania (I.L.L) is a nonpathogenic Leishmania strain. Due to its advantages, several recombinant proteins have been produced in this host. However, I.L.L shows a lower yield of recombinant protein expression compared to other commercial hosts. Considering the role of protease enzymes in protein digestion, we selected cysteine protease B (CPB) to investigate its impact on recombinant protein yield in I.L.L. Methods: we generated gene knockouts by utilizing homologous recombination (HR) and CRISPR methods. To assess the efficacy of the designed construct, we compared the yield of recombinant human factor VII (rhFVII) production between cells transfected with the pLEXSY-hyg2-FVII vector and the CMVpromoter-based construct (pF7cmvneo). Results: The knockout of a single CPB gene allele through the HR method or the complete knockout of all alleles through the CRISPR method led to cell death. This outcome suggests that even the deletion of a single CPB gene allele diminishes the protein to a level insufficient for the survival of I.L.L, indicating a critical dependency on the presence of this protein for the organism's viability. rhFVII exhibited a greater expression yield with the pLEXSY construct compared to the pF7cmvneo construct in I.L.L. The lower expression rate of pF7cmvneo may be influenced by epigenetic factors related to the CPC gene or the RNA polymerase used for the expression of that promoter. Conclusion: Therefore, considering alternative integration targets for CMVpromoter-based constructs and incorporating UTR sequences of I.L.L highexpression proteins in the vector may enhance recombinant protein expression rates. [ABSTRACT FROM AUTHOR]

The treatment of type 1 diabetes through islet cell transplantation is a complex process, facing challenges such as allograft rejections and a limited supply of donors. One potential solution is to utilize the liver as an alternative for natural insulin production, as hepatocytes can secrete proteins and respond to glucose levels. Recent research has shown promising results in using mesenchymal stem cells as a potential cure for diabetes. The study utilized a diabetic rat model, confirmed through blood sugar measurement. A plasmid vector was designed with specific genetic components, synthesized by biotech company, and then Inserted vector into a plasmid with resistance genes and bacterial origin. Bone marrow‐derived mesenchymal stem cells (BM‐MSCs) were cultured and transfected with the plasmid using Lipofectamine 3000. Polymerase chain reaction was employed to confirm successful transfection using specific primers. For the animal study, 30 male Wistar rats were divided into six groups, each comprising five rats. The control group did not receive any treatment, while the second group received MSCs via Portal Vein Injection. The third group received MSCs transfected with a specific construct via Portal Vein Injection. The fourth group was induced to develop diabetes through streptozotocin (STZ) injection, the fifth group developed diabetes and received untransfected MSCs via Portal Vein Injection, and the sixth group received MSCs transfected with the specific construct via Portal Vein Injection. To manage Pain, appropriate pain control was administered to the rats for 3 days after the surgery. Fixed liver tissues obtained from the euthanized rats were utilized for immunohistochemistry. In this study, immunohistochemical techniques were used to examine insulin expression in different groups of rats. The control groups showed high levels of insulin expression, while the diabetic groups exhibited lower expression. However, there was a significant difference between the diabetic groups treated with MSC and transgenic MSC cells. All groups had similar baseline glucose levels, but the diabetic groups showed a significant increase after STZ injection, whereas the control and MSC groups did not. Postintervention, both the control and MSC groups had similar glucose levels to the post‐STZ levels. However, diabetes‐induced groups experienced a significant decrease in glucose levels, with the transfected MSCs showing a greater decrease than the untransfected MSCs. The study suggested that treatment with MSCs, especially transfected ones, can effectively reduce glucose levels in rats with diabetes. In this research, rat BM‐MSCs were utilized to create insulin‐producing mesenchymal cells with glucose‐sensitive insulin expression. The cells were transferred to the liver of diabetic rats via portal vein injection, leading to an increase in insulin expression. This study proposes a novel approach for cell therapy and delivery in the treatment of type 1 diabetes. Significance Statement: Type 1 diabetes arises from autoimmune destruction of pancreatic β cells, leading to insulin deficiency. Cell therapy, presents a promising avenue. cells can be genetically engineered to produce insulin in response to glucose fluctuations. Mesenchymal stem cells are potential candidates for generating insulin‐producing cells. This study employed a novel approach, genetically engineered using a plasmid vector with glucose‐responsive elements in bone marrow‐derived mesenchymal stem cells and cell transfer to rat liver through portal vein injection. Differing from conventional methodologies, this research utilized undifferentiated rat BM‐MSCs. The hypothesis revolved around the potential of rat BM‐MSCs to migrate into the rat liver via the Portal Vein Injection method, offering a distinctive perspective on diabetes treatment. [ABSTRACT FROM AUTHOR]