학술논문

CCR5 Is a Therapeutic Target for Recovery after Stroke and Traumatic Brain Injury.
Document Type
article
Source
Cell. 176(5)
Subject
Motor Cortex
Neurons
Dendritic Spines
Animals
Mice
Inbred C57BL
Humans
Disease Models
Animal
Receptors
CCR5
Neuronal Plasticity
Aged
Aged
80 and over
Middle Aged
Female
Male
Cyclic AMP Response Element-Binding Protein
Stroke
Stroke Rehabilitation
Brain Injuries
Traumatic
MOCA
NIHSS
astrocyte
axon
axonal sprouting
dendritic spine
microglia
motor
premotor
Traumatic Head and Spine Injury
Aging
Behavioral and Social Science
Acquired Cognitive Impairment
Rehabilitation
Traumatic Brain Injury (TBI)
Brain Disorders
Physical Injury - Accidents and Adverse Effects
Stem Cell Research
Dementia
Stem Cell Research - Nonembryonic - Human
Neurosciences
Neurological
Mental health
Biological Sciences
Medical and Health Sciences
Developmental Biology
Language
Abstract
We tested a newly described molecular memory system, CCR5 signaling, for its role in recovery after stroke and traumatic brain injury (TBI). CCR5 is uniquely expressed in cortical neurons after stroke. Post-stroke neuronal knockdown of CCR5 in pre-motor cortex leads to early recovery of motor control. Recovery is associated with preservation of dendritic spines, new patterns of cortical projections to contralateral pre-motor cortex, and upregulation of CREB and DLK signaling. Administration of a clinically utilized FDA-approved CCR5 antagonist, devised for HIV treatment, produces similar effects on motor recovery post stroke and cognitive decline post TBI. Finally, in a large clinical cohort of stroke patients, carriers for a naturally occurring loss-of-function mutation in CCR5 (CCR5-Δ32) exhibited greater recovery of neurological impairments and cognitive function. In summary, CCR5 is a translational target for neural repair in stroke and TBI and the first reported gene associated with enhanced recovery in human stroke.