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COVID-19: How Does SARS-CoV-2 Infection Affect Vascular Irrigation of the Brain?

tissu cérébral humain post-mortem

Fluorescent image of post-mortem human brain tissue showing cell nuclei (blue) that reveal a blood vessel in which the vascular endothelial cells express the genetic material of SARS-CoV-2 (red). © Vincent Prévot/Inserm


A large number of researchers are currently mobilized to increase knowledge of SARS-CoV-2 in order to improve the treatment of infected patients and try to predict the future health impacts of infection with the virus. As part of an international collaboration, researchers from Inserm, Université de Lille, Lille University Hospital, and Pasteur Institute Lille within the Lille Neuroscience & Cognition laboratory, along with their colleagues from the CNRS1, have been the first to identify a direct effect of SARS-CoV-2 on the brain’s blood vessels. Certain cells, namely the cerebral vascular endothelial cells – essential components of the blood-brain barrier that protects the brain – are affected by a phenomenon of cell death. These findings, published in the journal Nature Neuroscience, particularly question the long-term impacts of the disease.

The blood vessels are comprised of endothelial cells. These include the vascular endothelial cells in the brain that make up the blood-brain barrier (BBB). The primary function of the BBB is to isolate the central nervous system from the bloodstream, preventing foreign substances or potentially toxic molecules from entering the brain and spinal cord while allowing the transfer of nutrients essential to their activity. As part of this effort, the vascular endothelial cells in the brain therefore play a key role in the proper irrigation of the organ, with their survival being essential for it to function correctly.

Within the framework of an international collaboration funded by the European Research Council3, the authors of the study looked at the vascular endothelial cells of the brain and the consequences of SARS-CoV-2 infection on their functioning.

Using preclinical research models and also by studying the cortex of patients who died as a result of SARS-CoV-2 infection, the researchers have shown that infection leads to the death of endothelial cells in the brain, resulting in the appearance of “ghost vessels” in the brain (empty tubes with no endothelial cells).

As a result, these essential cells can no longer perform their function in the BBB.

How does this endothelial cell death occur? What are the mechanisms involved? Thanks to state-of-the-art techniques2, the team has discovered that SARS-CoV-2 generates the manufacturing, from its own genetic material, of molecular scissors by the endothelial cells it infects. These scissors cleave a protein called NEMO which, being necessary for the endothelial cells to survive, therefore leads to their death.


The impacts of endothelial cell death on brain function

According to the scientists, the death of vascular endothelial cells in the brain can have two major consequences:

  • A temporary rupture of the BBB causing microbleeds in regions where the blood is not meant to have free access.
  • Hypoperfusion of some brain regions (due to the presence of non-functional ghost vessels), which is a decrease in blood flow that in the most serious cases can be fatal.

However, the study shows that the situation is reversible.

Furthermore, the scientists are interested in the long-term impacts of this phase of vulnerability during which brain irrigation is decreased. According to them, even if this hypothesis remains to be verified, this window of time could predispose certain people with the disease to develop cognitive or neurodegenerative disorders, or even dementia.

“This awareness of the severity of SARS-CoV-2 infection and its impacts on proper brain function is vital to enable the best possible management of infected patients in the years to come,” concludes Vincent Prévot, Inserm Research Director.


1 At the Center for Infection and Immunity of Lille (CNRS/Inserm/Institut Pasteur Lille/Université de Lille/Lille University Hospital)

2 Such as transgenesis, single-cell RNA sequencing, mass spectrometry and super-resolution microscopy.

3 Program funded by the European Research Council (ERC Synergy), with the participation of Drs. Prévot (Inserm, France), Nogueiras (University of Santiago de Compostela, Spain), and Schwaninger (University of Lübeck, Germany).

Researcher Contact

Vincent Prévot

Directeur de Recherche Inserm

Responsable de l’équipe « Développement et plasticité du cerveau neuroendocrine »

Unité U1172 – Lille Neuroscience & Cognition – Lille 

E-mail : rf.mresni@toverp.tnecniv

Téléphone sur demande

Press Contact



The SARS-CoV-2 main protease Mpro causes microvascular brain pathology by cleaving NEMO in brain endothelial cells


Jan Wenzel1,2*, Josephine Lampe1,2*, Helge Müller-Fielitz1 *, Raphael Schuster1 , Marietta Zille1,2, Kristin Müller1 , Markus Krohn1,2, Jakob Körbelin3 , Linlin Zhang4,5, Ümit Özorhan1,2, Vanessa Neve1, Julian U. G. Wagner2,6, Denisa Bojkova7 , Mariana Shumliakivska6 , Yun Jiang1 , Anke Fähnrich8,9, Fabian Ott8,9, Valentin Sencio10, Cyril Robil10, Susanne Pfefferle11, Florent Sauve12, Caio Fernando Ferreira Coêlho12, Jonas Franz13,14,15, Frauke Spiecker1 , Beate Lembrich1 , Sonja Binder1 , Nina Feller1,2, Peter König16,17, Hauke Busch8,9, Ludovic Collin18, Roberto Villaseñor18, Olaf Jöhren1, Hermann C. Altmeppen19, Manolis Pasparakis20, Stefanie Dimmeler2,6, Jindrich Cinatl7 , Klaus Püschel21, Matija Zelic22, Dimitry Ofengeim22, Christine Stadelmann13, François Trottein10, Ruben Nogueiras23, Rolf Hilgenfeld4,5, Markus Glatzel19, Vincent Prevot12, Markus Schwaninger1,2

Nature Neuroscience, octobre 2021