Skip to main content

Host Defense against Intracellular pathogens by Nitric Oxide

 

New paradigm of host defense against intracellular pathogens by nitric oxide]



Free article

Abstract

Nitric oxide (NO) produced by inducible NO synthase (iNOS) during infection plays a crucial role in host defense mechanisms, via its antimicrobial and cytoprotective activities. Infection of Salmonella typhimurium in mice induces excessive production of NO, as a host defense response. We found much greater bacterial growth and apoptotic changes in iNOS-deficient (iNOS-/-) mice than in wild-type mice. However, the mechanism of NO-mediated cytoprotection during Salmonella infection remained unclear. An important signaling mechanism induced by NO is heme oxygenase (HO)-1, a significant cytoprotective molecule produced by oxidative stress. Thus, we sought to clarify NO-dependent cytoprotective and antimicrobial host defense, with a particular focus on the signaling mechanism of HO-1 induction. We recently discovered a nitrated cyclic nucleotide, 8-nitroguanosine 3',5'-cyclic monophosphate (8-nitro-cGMP), which is formed via NO possibly with reactive oxygen species. We observed strong immunoreactivity for 8-nitro-cGMP in Salmonella-infected wild-type mouse liver and peritoneal macrophages in culture but not in iNOS-/- mouse liver and macrophages. Moreover, a higher apoptosis was observed in iNOS-/- macrophages compared with wild-type macrophages after Salmonella infection, but the difference was nullified when iNOS-/- cells were treated with 8-nitro-cGMP. Finally, authentic 8-nitro-cGMP induced HO-1 in cultured macrophages infected with Salmonella. The signaling function of 8-nitro-cGMP appears to be mediated by its unique reaction with the sulfhydryl group of cysteine, thus forming a proteinS-cGMP adduct, which is an important mechanism of post-translational modification of proteins called protein S-guanylation. More importantly, we found 8-nitro-cGMP-dependent S-guanylation of Keap1, a regulatory protein of transcription factor Nrf2, which regulates the transcription of HO-1. In this review, we focus on a unique mechanism of NO-mediated host defense via formation of a novel signaling molecule, 8-nitro-cGMP in microbial infections.

Comments

Popular posts from this blog

Patrick Gut Environment

\ Keywords to use in further research, GALT, tight junction proteins, Mucin layer, microbiome in MECFS or Long Covid, Goblet cells.   It was great chatting with you the other day. I’ve put together this general overview, but as I mentioned, you’ll definitely want to do your own deeper research. This is a very complex, interactive environment, and you’ll naturally come across many different opinions about what’s happening. Most opinions tend to focus on single layers, but as I’ve discovered, these layers are highly interconnected and influence one another. I don’t want to oversimplify things, nor do I want to overcomplicate them. It takes time to truly understand the gut environment in its proper context. I’m also cautious about saying “do X and you’ll get Y,” because results are rarely that straightforward. When I introduce layered therapies, I look for subtle changes across a list of markers I track. That’s why I believe this should be approached with care and patience—though I’m ...

Gut environment

 OK let's go back over the scenario Somebody gets a gut bug that could be viral or bacterial and we're going to put in the context of either long COVID or MECFS Let's discuss what exactly happens of how the body begins to adapt to this insult p — let’s build this cleanly, structurally, and without drama. This is the core terrain‑mechanics model of what happens when someone gets a gut bug (viral or bacterial) and then develops a long‑tail condition like long COVID or ME/CFS . This is the architecture that explains why the system never fully resets . I’ll walk you through it in chronological order , layer by layer, so you can see exactly how the body adapts — and why those adaptations become the trap. ⭐ 1. The Initial Insult Terrain layer: immune activation, epithelial irritation, redox stress A viral or bacterial gut infection does three things immediately: damages epithelial cells strips mucin spikes inflammatory cytokines This creates: redox collapse increased permeabil...

Paneth Cells - guardians of the intestinal tract

  Click for the AI slideshow: https://sl.bing.net/hBioK3sTdDw From Google Gemini: Paneth Cells: The Guardians of the Gut Paneth cells are specialized epithelial cells found at the base of the intestinal crypts (small invaginations in the intestinal lining). They play a crucial role in maintaining the gut's health by acting as a first line of defense against harmful microorganisms. Key Functions: Antimicrobial Defense: Paneth cells produce and secrete a variety of antimicrobial peptides and proteins, such as lysozyme, defensins, and phospholipase A2. These substances help to kill bacteria, fungi, and other pathogens that may invade the intestinal tract. Regeneration of Intestinal Epithelium: Paneth cells contribute to the maintenance and regeneration of the intestinal lining by supporting the stem cells located nearby. Immune Regulation: These cells participate in regulating the immune response within the gut, helping to balance the body's reaction to both beneficial and ha...