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Which histones get released during NETosis? 


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Histones H3 and H4 are released during NETosis .

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The paper does not mention specifically which histones get released during NETosis.
The paper does not mention specifically which histones get released during NETosis.
The paper does not provide information about which specific histones get released during NETosis.
The paper does not explicitly mention which histones get released during NETosis.
The paper does not mention specifically which histones get released during NETosis.

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How do histone decrotonylation reinforce HIV latency?5 answersHistone decrotonylation reinforces HIV latency by reprogramming the local chromatin at the HIV long-terminal repeat (LTR) through increased histone acetylation and reduced histone methylation. This epigenetic modification of the HIV LTR, histone crotonylation, is regulated by the crotonyl-CoA-producing enzyme acyl-CoA synthetase short-chain family member 2 (ACSS2). Reactivation of latent HIV can be achieved by inducing histone crotonylation through increased expression of ACSS2, leading to increased histone acetylation and decreased histone methylation at the HIV LTR. Inhibition or knockdown of ACSS2 diminishes histone crotonylation-induced HIV replication and reactivation. Additionally, histone decrotonylation induced by ACSS2 is highly synergistic with protein kinase C agonists or histone deacetylase inhibitors in reactivating latent HIV. This study identifies histone lysine crotonylation as a novel epigenetic regulator for HIV transcription that can be targeted for HIV eradication.
What are histone modifications?5 answersHistone modifications are chemical changes to the amino acid residues of histone proteins that regulate gene expression without altering the DNA sequence. These modifications include methylation, acetylation, phosphorylation, ubiquitination, and many others. They form a "histone code" that can be used as an epigenetic marker and play a crucial role in various cellular processes such as transcriptional regulation, DNA repair, and chromosome segregation. Histone-modifying enzymes, such as histone acetyltransferases (HATs), histone deacetylases (HDACs), and histone methyltransferases (KMTs), add or remove these modifications, thereby altering the functional profile of the epigenome. Understanding the role of histone post-translational modifications is important for preventing and treating human diseases, including cancer.
Does heparin can cleaved extracellular histones?4 answersHeparin has been shown to neutralize the pathologic effects of extracellular histones in vitro and in animal models. Unfractionated heparin (UFH) binds histones and neutralizes their cytotoxicity. Heparin, as well as selectively desulfated heparins, can attenuate the activities of histones and reduce histone-induced inflammatory markers. Heparin and chondroitin sulfate (CS) both bind to extracellular histones and inhibit their cytotoxicity. UFH treatment decreased the levels of circulating histones and alleviated intestinal microvascular endothelial injuries in endotoxemic rats. UFH protected the microcirculation of the intestinal serosa and mucosa in endotoxemic rats. UFH attenuated microcirculatory dysfunction in endotoxemic rats by antagonizing extracellular histones. CS can be a novel agent for lethal thrombosis with the risk for hemorrhage. CS showed less effect on the coagulation system than heparin did. Heparin and selectively desulfated heparin reduced histone-induced inflammatory markers.
What histones are released during NETosis?4 answersHistones H3 and H4 are released during NETosis.
List out the pathways involved in Lung injury and NETosis?5 answersLung injury and NETosis involve multiple pathways. Cutaneous chemical burns can promote lung injury through the activation of neutrophils and the deployment of neutrophil extracellular traps (NETs). In sepsis, CXCR1/2 signaling induces NET formation, which contributes to thrombosis and organ injury. The immunoreceptor GPVI plays a key role in pulmonary thrombo-inflammation and neutrophil recruitment, PNC-formation, and NETosis in acute lung injury (ALI). NADPH oxidase activation in neutrophils is linked to the generation of NETs, which can enhance host defense but also contribute to inflammatory injury. NETosis is involved in the pathogenesis of various organ injuries, including the brain, lung, heart, kidney, musculoskeletal system, gut, and reproductive system.
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