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NG2‐glia crosstalk with microglia in health and disease
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AbstractNeurodegenerative diseases are increasingly becoming a global problem. However, the pathological mechanisms underlying neurodegenerative diseases are not fully understood. NG2‐glia abnormalities and microglia activation are involved in the development and/or progression of neurodegenerative disorders, such as multiple sclerosis, Alzheimer's disease, Parkinson's disease, and cerebrovascular diseases. In this review, we summarize the present understanding of the interaction between NG2‐glia and microglia in physiological and pathological states and discuss unsolved questions concerning their fate and potential fate. First, we introduce the NG2‐glia and microglia in health and disease. Second, we formulate the interaction between NG2‐glia and microglia. NG2‐glia proliferation, migration, differentiation, and apoptosis are influenced by factors released from the microglia. On the other hand, NG2‐glia also regulate microglia actions. We conclude that NG2‐glia and microglia are important immunomodulatory cells in the brain. Understanding the interaction between NG2‐glia and microglia will help provide a novel method to modulate myelination and treat neurodegenerative disorders.
Title: NG2‐glia crosstalk with microglia in health and disease
Description:
AbstractNeurodegenerative diseases are increasingly becoming a global problem.
However, the pathological mechanisms underlying neurodegenerative diseases are not fully understood.
NG2‐glia abnormalities and microglia activation are involved in the development and/or progression of neurodegenerative disorders, such as multiple sclerosis, Alzheimer's disease, Parkinson's disease, and cerebrovascular diseases.
In this review, we summarize the present understanding of the interaction between NG2‐glia and microglia in physiological and pathological states and discuss unsolved questions concerning their fate and potential fate.
First, we introduce the NG2‐glia and microglia in health and disease.
Second, we formulate the interaction between NG2‐glia and microglia.
NG2‐glia proliferation, migration, differentiation, and apoptosis are influenced by factors released from the microglia.
On the other hand, NG2‐glia also regulate microglia actions.
We conclude that NG2‐glia and microglia are important immunomodulatory cells in the brain.
Understanding the interaction between NG2‐glia and microglia will help provide a novel method to modulate myelination and treat neurodegenerative disorders.
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