TY - JOUR
T1 - Imaging a concussion and the ensuing immune response at the blood–brain barrier
AU - Nguyen, Rita H.
AU - Newton, Michelle
AU - Kratofil, Rachel M.
AU - Scott, Brittney N.V.
AU - Castanheira, Fernanda
AU - Jung-Seok, Kim
AU - Ginhoux, Florent
AU - Jung, Steffen
AU - Kubes, Paul
N1 - Publisher Copyright:
Copyright © 2025 the Author(s). Published by PNAS.
PY - 2025/5/27
Y1 - 2025/5/27
N2 - Concussions can cause debilitating symptoms despite no evidence of structural changes on diagnostic imaging. The cellular events occurring in the brain parenchyma following concussion, especially repetitive concussion, are not well elucidated. We developed a concussion model to induce a confined area of injury without causing frank hemorrhage. Using intravital microscopy, we observe activation of the vasculature that supported neutrophil rolling and platelet adhesion but no overt cellular recruitment from blood into brain parenchyma. Activated resident, not monocyte-derived, macrophages relocated to the injury site via Cx3cr1 and phagocytosed dysfunctional/ detached astrocytes via scavenger receptors and TLR4, particularly after repetitive concussion. Additionally, microglia sealed areas of blood–brain barrier (BBB) disruption via purinergic pathways. Using a splitCre approach to dissect microglia and perivascular macrophages, we show that microglial invasion into the injury site is key to reducing BBB disruption. Our data suggest that microglia repair the BBB following concussion, but in doing so significantly alter the cellular ultrastructure of the brain milieu.
AB - Concussions can cause debilitating symptoms despite no evidence of structural changes on diagnostic imaging. The cellular events occurring in the brain parenchyma following concussion, especially repetitive concussion, are not well elucidated. We developed a concussion model to induce a confined area of injury without causing frank hemorrhage. Using intravital microscopy, we observe activation of the vasculature that supported neutrophil rolling and platelet adhesion but no overt cellular recruitment from blood into brain parenchyma. Activated resident, not monocyte-derived, macrophages relocated to the injury site via Cx3cr1 and phagocytosed dysfunctional/ detached astrocytes via scavenger receptors and TLR4, particularly after repetitive concussion. Additionally, microglia sealed areas of blood–brain barrier (BBB) disruption via purinergic pathways. Using a splitCre approach to dissect microglia and perivascular macrophages, we show that microglial invasion into the injury site is key to reducing BBB disruption. Our data suggest that microglia repair the BBB following concussion, but in doing so significantly alter the cellular ultrastructure of the brain milieu.
KW - astrocytes
KW - blood–brain barrier
KW - concussion
KW - microglia
KW - traumatic brain injury
UR - http://www.scopus.com/inward/record.url?scp=105005897801&partnerID=8YFLogxK
U2 - 10.1073/pnas.2414316122
DO - 10.1073/pnas.2414316122
M3 - Article
C2 - 40388609
AN - SCOPUS:105005897801
SN - 0027-8424
VL - 122
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 21
M1 - e2414316122
ER -