TY - JOUR
T1 - Age-dependent immune and lymphatic responses after spinal cord injury
AU - Salvador, Andrea Francesca M.
AU - Dykstra, Taitea
AU - Rustenhoven, Justin
AU - Gao, Wenqing
AU - Blackburn, Susan M.
AU - Bhasiin, Kesshni
AU - Dong, Michael Q.
AU - Guimarães, Rafaela Mano
AU - Gonuguntla, Sriharsha
AU - Smirnov, Igor
AU - Kipnis, Jonathan
AU - Herz, Jasmin
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/7/19
Y1 - 2023/7/19
N2 - Spinal cord injury (SCI) causes lifelong debilitating conditions. Previous works demonstrated the essential role of the immune system in recovery after SCI. Here, we explored the temporal changes of the response after SCI in young and aged mice in order to characterize multiple immune populations within the mammalian spinal cord. We revealed substantial infiltration of myeloid cells to the spinal cord in young animals, accompanied by changes in the activation state of microglia. In contrast, both processes were blunted in aged mice. Interestingly, we discovered the formation of meningeal lymphatic structures above the lesion site, and their role has not been examined after contusive injury. Our transcriptomic data predicted lymphangiogenic signaling between myeloid cells in the spinal cord and lymphatic endothelial cells (LECs) in the meninges after SCI. Together, our findings delineate how aging affects the immune response following SCI and highlight the participation of the spinal cord meninges in supporting vascular repair.
AB - Spinal cord injury (SCI) causes lifelong debilitating conditions. Previous works demonstrated the essential role of the immune system in recovery after SCI. Here, we explored the temporal changes of the response after SCI in young and aged mice in order to characterize multiple immune populations within the mammalian spinal cord. We revealed substantial infiltration of myeloid cells to the spinal cord in young animals, accompanied by changes in the activation state of microglia. In contrast, both processes were blunted in aged mice. Interestingly, we discovered the formation of meningeal lymphatic structures above the lesion site, and their role has not been examined after contusive injury. Our transcriptomic data predicted lymphangiogenic signaling between myeloid cells in the spinal cord and lymphatic endothelial cells (LECs) in the meninges after SCI. Together, our findings delineate how aging affects the immune response following SCI and highlight the participation of the spinal cord meninges in supporting vascular repair.
KW - immune response to injury
KW - lymphatics
KW - macrophages
KW - meninges
KW - microglia
KW - neuroimmunology
KW - spinal cord injury
UR - http://www.scopus.com/inward/record.url?scp=85163143376&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2023.04.011
DO - 10.1016/j.neuron.2023.04.011
M3 - Article
C2 - 37148871
AN - SCOPUS:85163143376
SN - 0896-6273
VL - 111
SP - 2155-2169.e9
JO - Neuron
JF - Neuron
IS - 14
ER -