The red blood cells contain a full complement of sodium transporters and cotransporters and

since the RBC plasma membranes were utilized initially in the early studies of sodium transport, I am thinking that sodium transport may be involved once the SARS-CoV-2 binds to the red blood cells via CD147 once it has established the viremic stage of end-organ or distant organ infection i.e. heart kidney vessel and brain and skeletal muscle with marked muscular pain reported by individuals with early COVID-19.

The red blood cell(s) (RBC) are unique in that they are anuclear and do not contain a nucleus that is required for SARS-CoV-2 virus to replicate and therefore RBCs may act as a carrier vehicle to spread the disease to other organs in addition to the WBCs.

Viremia or Virion sepsis is a multi-step process that can be supported with both light and electron microscopy.

RBCs have numeruous receptors and channels on them and I am interested in the eNOS enzyme

and if it has the capibility to secrete No from the eNOS enzyme to assist in normal endothelial cell function...??? Also since SARS-CoV-2 can cause hemoglobin to split into toxic heme and iron and result in hypercoagulopathy state that we need to learn more about RBC physiology especially as it pertains to the COVID-19 pandemic.

This discussion and or question is now open for any and all comments and suggestions as to how to proceed with this fascinating concept.

Melvin R Hayden

University of MIssouri School of Medicine

Columbia, Missouri

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