2/ Contribution of Extracellular DNA to Venous Thrombosis:
DNA is involved in causing blood clots in veins, specifically in animal experiments. DNA was found in blood clots along with other substances.
Extracellular DNA plays a role in causing blood clots in veins.
3/ Contribution of Extracellular DNA to Arterial Thrombosis
Several studies using animal models show extracellular DNA can cause blood clots in arteries. In mice with atherosclerosis (a condition where arteries get blocked), using a substance called DNase I reduced the amount
4/of blockage in the arteries. Additionally, in a mouse model of cholesterol embolism (blockage caused by cholesterol crystals), extracellular DNA was found to be a crucial component in forming clots when arteries became blocked.
5/ Extracellular DNA in Ischemic Stroke
In stroke patients, there is evidence of extracellular DNA in the brain, which might play a role in causing strokes. Analysis of blood clots taken from stroke patients revealed the presence of many nucleated white blood cells,
6/especially neutrophils, and structures called NETs in these clots.
I mice, in experiments that mimicked stroke conditions, higher levels of DNA and nucleosomes circulating in the blood were found after a stroke. When the brain lacks oxygen ( hypoxia), there is even more
7/extracellular chromatin (the material DNA is made of). Importantly, when researchers used a substance called DNase I to break down this extracellular chromatin, it improved the outcome of the stroke.
8/ 🚨🚨🚨🚨🚨Extracellular DNA to Thrombus Formation in the Microvasculature
Recent studies show extracellular DNA plays a significant role in causing organ dysfunction in conditions like disseminated intravascular coagulation (DIC). This dysfunction is
9/ due to high levels of circulating thrombin, increased platelet clumping, leakage from blood vessels, the release of proinflammatory substances, and the formation of structures known as neutrophil extracellular traps (NETs).
10/ In cases of sepsis-induced DIC, large numbers of NETs tend to accumulate mainly in the tiny blood vessels of the lung and liver. Studies using mice lacking the enzyme DNase, which breaks down DNA, found that NET clots were linked to thrombotic microangiopathy (TMA) and DIC,
11/ characterized by broken red blood cells, anemia, and organ failure due to blood vessel blockages. Similar findings were seen in patients with severe bacterial infections.
Observations using advanced microscopy techniques showed that, in septic tissues, there were aggregated
12/ platelets, fibrin clots, and extracellular DNA together. The process of NETosis, the formation of NETs, is regulated by an enzyme called peptidyl arginine deiminase 4 (PAD4), which modifies histones in a way that loosens DNA structure.
13/ What this means: Microvasculature are the smallest blood vessels in the circulatory system, including arterioles, venules, and capillaries.
Disseminated Intravascular Coagulation (DIC) is a serious medical condition that affects the body's ability to regulate blood clotting
14/ In a healthy person, blood clotting is a necessary and controlled process that helps stop bleeding when there is an injury. However, in DIC, this process becomes chaotic and dysfunctional.
Normally, when you get injured, your body forms blood clots to prevent excessive
15/bleeding. This process involves a series of proteins and cells in your blood working together to create a clot at the site of injury.
In DIC, something triggers an abnormal and excessive activation of this clotting process throughout your bloodstream.
16/🚨🚨🚨In this case the DNA plasmid contamination can cause DIC.
Because the clotting process becomes overactive, small blood clots form within blood vessels throughout the body.
17/ These clots can block blood flow to vital organs and tissues, leading to organ damage and potentially life-threatening complications.
Paradoxically, this excessive clotting can also lead to a depletion of clotting factors and platelets in the blood. As a result, the ability
18/ to form clots when needed is compromised, which can lead to uncontrolled bleeding in some parts of the body.
clots in the microvasculature, can also cause neuropathy. Neuropathy refers to damage or dysfunction of the peripheral nerves, and it can lead to various symptoms,
19/Including pain, tingling, numbness, and weakness in the affected areas.
When clots form in the microvasculature, they can disrupt the blood supply to nerves, depriving them of oxygen and nutrients. This lack of blood flow can lead to nerve damage, which in turn can result in
20/ neuropathic symptoms. Clots can also directly compress or injure nerves, causing neuropathy.
Vasculitis: Inflammatory condition that affect blood vessels can lead to microvascular clots and nerve damage. This can also cause neuropathy.
CpG when in a negative charged LNP
21/ Can bund to the inside of capillaries, (see previous threads), remodel the tight junctions, loosen them, cause the LNP to weaken the micro vasculature, and cause damage in the endothelial cells, and also cause the spike protein that is expressed from RNA which is injected
22/ into the body, to express there causing a multi fold attack by the immune system, causing the body to attach that area, due to both spike presence and CpG motif in the plasmid DNA contamination that is there, along with the presence of both positive and negatively charged
1/ 🚨🧵DNA plasmid contamination in modRNA "vaccines"
DO NOT HAVE TO ENTER THE NUCLEUS
to impact
GENE EXPRESSION, and be implicated in CANCER RISK!
(I said this on April Moss TV MONTHS ago talking about proteomics and gene expression!)
STUDY BELOW in somewhat LAYMAN'S TERMS
2/ Study citation: Gao JJ, Diesl V, Wittmann T, Morrison DC, Ryan JL, Vogel SN, Follettie MT. Bacterial LPS and CpG DNA differentially induce gene expression profiles in mouse macrophages. J Endotoxin Res. 2003;9(4):237-43. doi: 10.1179/096805103225001431. PMID: 12935354.
3/ In the study, the researchers investigated the impact of CpG DNA and LPS on gene expression. They exposed macrophages to CpG DNA and LPS (lipopolysaccharide), which are known immune stimulants. CpG DNA is recognized by Toll-like receptor 9 (TLR9) and can
1/ 🚨 OMG!
Introducing foreign DNA Plasmid into THE DEVELOPING BRAINS
of mice can lead to
SEIZURES, DAMAGE in brain development, such as consequences on microglia behavior, which could cause brain abnormalities, various cognitive disorders, cerebral palsy, neuronal damage!
2/ The study: 2018
Neocortical Microglia Express Toll-Like Receptor 9 and Respond to Plasmid DNA Injected into the Ventricle: Technical Considerations Regarding Microglial Distribution in Electroporated Brain Walls eneuro.org/content/5/6/EN…
3/ These researchers raise concerns about the unintended effects of introducing genetic material into the developing brain, specially PLASMID DNA In humans, it could suggest that when manipulating genes or introducing foreign genetic material during early brain development,
1/ 🚨🚨🚨🚨🚨
The presence of CpG motifs (DNA plasmid contamination) STUDY:
Angiogenesis is the process of forming new blood vessels.
CpG motifs inhibits angiogenesis.
This means the CpG motif in DNA plasmids prevents or slows down the formation of new blood vessels.
2/ Pleiotropic action of CpG-ODN on endothelium and macrophages attenuates angiogenesis through distinct pathways
Jiahui Wu,1 Wenru Su,2,3 Michael B. Powner,4 Jian Liu,1 David A. Copland,1 Marcus Fruttiger,4 Paolo Madeddu,5 Andrew D. Dick,1,4,6 and Lei Liua,1
1/ 🚨🚨 Liver Injury after exposure to CpG motif (The DNA plasmid contamination in RNA injection contains large segments of CpG motifs).
ONE DAY after CpG-ODN application to the liver, there were significant negative effects on the liver's microcirculation and function/injury.
2/ The study:
CD205-TLR9-IL-12 axis contributes to CpG-induced oversensitive liver injury in HBsAg transgenic mice by promoting the interaction of NKT cells with Kupffer cells nature.com/articles/cmi20…
3/ Kupffer cells are liver-resident macrophages located in the liver sinusoid. They represent the largest population of immune cells in the liver and serve as the first line of defense against pathogens entering the liver via the portal vein. They recognize pathogens through
2/ the authors aimed to investigate the role of bacterial DNA in causing brain inflammation. This study looks at the same "motif" that is contained within the recent discovery of the DNA plasmid contamination, what is called a CpG motif. A CpG motif, also known as a CpG X
3/A CpG motif, also known as a CpG dinucleotide, is a sequence of two DNA nucleotides in which a cytosine (C) is followed by a guanine (G). The "p" in CpG stands for the phosphodiester bond that links these two nucleotides in the DNA molecule.
But if that is glazing your eyes
1/ Nuclear uptake of plasmid DNA is one of the many cellular barriers that limit the efficiency of non-viral gene delivery systems. We have determined the number of plasmids that reach the nucleus of a transfected cell using an internally standardized quantitative PCR (qPCR) assay.
@LionAdvocacy @DrSusanOliver1 @P_J_Buckhaults 2/
@LionAdvocacy @DrSusanOliver1 @P_J_Buckhaults 3/
Formation and Intracellular Trafficking of Lipoplexes and Polyplexes cell.com/molecular-ther…