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Targeting pericytes for therapeutic approaches to neurological disorders

期刊

ACTA NEUROPATHOLOGICA
卷 136, 期 4, 页码 507-523

出版社

SPRINGER
DOI: 10.1007/s00401-018-1893-0

关键词

Pericyte; Capillary; Blood-brain barrier; Ischaemia; Alzheimer's; Spinal cord injury; Diabetes

资金

  1. European Research Council (BrainEnergy)
  2. Wellcome Trust [099222/Z/12/Z]
  3. BBSRC
  4. Leonard Wolfson Experimental Neurology Centre
  5. Rosetrees Trust
  6. National Natural Science Foundation of China [81622041]
  7. National Key R&D Program of China [2017YFC1307500, 2017YFC1307504]
  8. Wellcome Trust [099222/Z/12/Z] Funding Source: Wellcome Trust
  9. Wellcome Trust [099222/Z/12/Z] Funding Source: researchfish

向作者/读者索取更多资源

Manycentral nervous system diseases currently lack effective treatment and are often associated with defects in microvascular function, including a failure to match the energy supplied by the blood to the energy used on neuronal computation, or a breakdown of the blood-brain barrier. Pericytes, an under-studied cell type located on capillaries, are of crucial importance in regulating diverse microvascular functions, such as angiogenesis, the blood-brain barrier, capillary blood flow and the movement of immune cells into the brain. They also form part of the glial scar isolating damaged parts of the CNS, and may have stem cell-like properties. Recent studies have suggested that pericytes play a crucial role in neurological diseases, and are thus a therapeutic target in disorders as diverse as stroke, traumatic brain injury, migraine, epilepsy, spinal cord injury, diabetes, Huntington's disease, Alzheimer's disease, diabetes, multiple sclerosis, glioma, radiation necrosis and amyotrophic lateral sclerosis. Here we report recent advances in our understanding of pericyte biology and discuss how pericytes could be targeted to develop novel therapeutic approaches to neurological disorders, by increasing blood flow, preserving blood-brain barrier function, regulating immune cell entry to the CNS, and modulating formation of blood vessels in, and the glial scar around, damaged regions.

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