Protective roles for myeloid cells in neuroinflammation.
Trevor OwensAnouk Benmamar-BadelAgnieszka WlodarczykJoanna MarczynskaMarlene T MørchMagdalena DubikDina S ArengothNasrin AsgariGill WebsterReza KhorooshiPublished in: Scandinavian journal of immunology (2020)
Myeloid cells represent the major cellular component of innate immune responses. Myeloid cells include monocytes and macrophages, granulocytes (neutrophils, basophils and eosinophils) and dendritic cells (DC). The role of myeloid cells has been broadly described both in physiological and in pathological conditions. All tissues or organs are equipped with resident myeloid cells, such as parenchymal microglia in the brain, which contribute to maintaining homeostasis. Moreover, in case of infection or tissue damage, other myeloid cells such as monocytes or granulocytes (especially neutrophils) can be recruited from the circulation, at first to promote inflammation and later to participate in repair and regeneration. This review aims to address the regulatory roles of myeloid cells in inflammatory diseases of the central nervous system (CNS), with a particular focus on recent work showing induction of suppressive function via stimulation of innate signalling in multiple sclerosis (MS) and its animal model experimental autoimmune encephalomyelitis (EAE).
Keyphrases
- dendritic cells
- induced apoptosis
- immune response
- cell cycle arrest
- multiple sclerosis
- oxidative stress
- bone marrow
- acute myeloid leukemia
- endoplasmic reticulum stress
- gene expression
- stem cells
- spinal cord injury
- signaling pathway
- transcription factor
- regulatory t cells
- cell proliferation
- ms ms
- spinal cord
- peripheral blood
- blood brain barrier
- neuropathic pain
- wound healing
- cerebral ischemia