Bioasis

Headquarters for T cell production: Thymus organ controls T cell production by creating Thymus peptides. T cells become exhausted when their mitochondrial battery fails.

Healthy T Cells kill infected cells. Those dying cells are absorbed and degraded into basic building blocks by M2 Macrophages. Autophagy redistributes those building blocks to healthy cells.

Senescent cells can release 150x more inflammation than normal cells called SASP. NK Cells are attracted by SASP to kill the senescent cell.

Those dying senescent cells are absorbed and degraded into basic building blocks by M2 Macrophages during efferocytosis.

Microplastics, fatty plaques, trans fats, and more are increasing the burden of scavenging lipid cores by phagocytotic macrophages.

By leveraging M2 macrophages and their surface receptors, we can accelerate efferocytosis and target foreign particles like microplastics or plaques to reduce overall plaque volume at a faster rate than statins.

Vitamin K2 is known for its ability to target calcification in arteries. K2 actually achieves this through a protein called MGP.

Matrix Gla-Protein (MGP) can be fragmented into peptides that can reduce the development of calcification.

Valvular dysfunction and ventricle hypertrophy are common forms of cardiac degeneration that happen during aging.

By removing fibrotic scars while regenerating healthy collagens, we may be able to restabilize the elasticity of valves and ventricles while minimizing hypertrophy and valvular prolapse.

Many diseases from MS to ALS and Alzheimer's are caused by neurodegeneration in different areas of the brain.

Removing plaques, glial scars, and calcification while restoring stem cell supply with neurogenic growth factors may pave a path to restoring brain functionality.