Astrocyte Activation in Neurovascular Damage and Repair Following Ischaemic Stroke.
Adjanie PatabendigeAyesha SinghStuart Iain JenkinsJon SenRuoli ChenPublished in: International journal of molecular sciences (2021)
Transient or permanent loss of tissue perfusion due to ischaemic stroke can lead to damage to the neurovasculature, and disrupt brain homeostasis, causing long-term motor and cognitive deficits. Despite promising pre-clinical studies, clinically approved neuroprotective therapies are lacking. Most studies have focused on neurons while ignoring the important roles of other cells of the neurovascular unit, such as astrocytes and pericytes. Astrocytes are important for the development and maintenance of the blood-brain barrier, brain homeostasis, structural support, control of cerebral blood flow and secretion of neuroprotective factors. Emerging data suggest that astrocyte activation exerts both beneficial and detrimental effects following ischaemic stroke. Activated astrocytes provide neuroprotection and contribute to neurorestoration, but also secrete inflammatory modulators, leading to aggravation of the ischaemic lesion. Astrocytes are more resistant than other cell types to stroke pathology, and exert a regulative effect in response to ischaemia. These roles of astrocytes following ischaemic stroke remain incompletely understood, though they represent an appealing target for neurovascular protection following stroke. In this review, we summarise the astrocytic contributions to neurovascular damage and repair following ischaemic stroke, and explore mechanisms of neuroprotection that promote revascularisation and neurorestoration, which may be targeted for developing novel therapies for ischaemic stroke.
Keyphrases
- cerebral ischemia
- subarachnoid hemorrhage
- brain injury
- blood brain barrier
- oxidative stress
- cerebral blood flow
- induced apoptosis
- atrial fibrillation
- small molecule
- resting state
- white matter
- single cell
- magnetic resonance imaging
- spinal cord
- electronic health record
- spinal cord injury
- big data
- cell therapy
- magnetic resonance
- cell proliferation
- artificial intelligence
- cancer therapy
- contrast enhanced
- bone marrow
- cell death
- mesenchymal stem cells