Alzheimer's disease
Aug 7, 2024 1:07:45 GMT
Post by Admin on Aug 7, 2024 1:07:45 GMT
So we're talking about Alzheimer's disease now;
pubmed.ncbi.nlm.nih.gov/35259518/
"Nuclear and cellular, micro and nano calcification in Alzheimer's disease patients and correlation to phosphorylated Tau"
Tau is a microtubule associated protein and it's deposition in the brain is a marker for AD. Microtubules are cellular support filaments that have been shown to be deconstructed by Bartonella and the components relocated to the plasma membrane.
journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008548
"Bartonella effector protein C mediates actin stress fiber formation via recruitment of GEF-H1 to the plasma membrane"
"Our data support a model in which BepC activates the RhoA/ROCK pathway by re-localization of GEF-H1 from microtubules to the plasma membrane."
This is also the material tat bartonella uses to create vacuoles inside cells and those vacuoles protect it from antibiotics, it uses the cytoskeleton proteins.
www.nature.com/articles/ncb773
"Nucleotide exchange factor GEF-H1 mediates cross-talk between microtubules and the actin cytoskeleton"
These effector proteins introduce genetic changes to the cell and Bep C clearly is involved in the deconstruction of microtubules and other cytoskeleton proteins of which Tau proteins are fundamental components.
The calcification aspect is already well described and Bartonella is a calcifying bacteria and that was first described by Olavi Kajander and Neva Çiftçioglu and they included Bartonella in their definition of Nanobacteria;
www.pnas.org/doi/10.1073/pnas.95.14.8274
“Nanobacteria: An alternative mechanism for pathogenic intra- and extracellular calcification and stone formation”
“nanobacteria fall within the α-2 subgroup of Proteobacteria, which also includes Brucella and Bartonella species”
Calcification;
bartonella.freeforums.net/thread/124/calcification
~d
pubmed.ncbi.nlm.nih.gov/35259518/
"Nuclear and cellular, micro and nano calcification in Alzheimer's disease patients and correlation to phosphorylated Tau"
Tau is a microtubule associated protein and it's deposition in the brain is a marker for AD. Microtubules are cellular support filaments that have been shown to be deconstructed by Bartonella and the components relocated to the plasma membrane.
journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008548
"Bartonella effector protein C mediates actin stress fiber formation via recruitment of GEF-H1 to the plasma membrane"
"Our data support a model in which BepC activates the RhoA/ROCK pathway by re-localization of GEF-H1 from microtubules to the plasma membrane."
This is also the material tat bartonella uses to create vacuoles inside cells and those vacuoles protect it from antibiotics, it uses the cytoskeleton proteins.
www.nature.com/articles/ncb773
"Nucleotide exchange factor GEF-H1 mediates cross-talk between microtubules and the actin cytoskeleton"
These effector proteins introduce genetic changes to the cell and Bep C clearly is involved in the deconstruction of microtubules and other cytoskeleton proteins of which Tau proteins are fundamental components.
The calcification aspect is already well described and Bartonella is a calcifying bacteria and that was first described by Olavi Kajander and Neva Çiftçioglu and they included Bartonella in their definition of Nanobacteria;
www.pnas.org/doi/10.1073/pnas.95.14.8274
“Nanobacteria: An alternative mechanism for pathogenic intra- and extracellular calcification and stone formation”
“nanobacteria fall within the α-2 subgroup of Proteobacteria, which also includes Brucella and Bartonella species”
Calcification;
bartonella.freeforums.net/thread/124/calcification
~d