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Published on: October 13, 2023
Novel feedback loop between M2 macrophages/microglia and regulatory B cells in estrogen-protected EAE mice
Gil Benedek1, Jun Zhang1, Ha Nguyen1
1Neuroimmunology Research, VA Portland Health Care System, 3710 SW U.S. Veterans Hospital Rd., Portland, OR 97239, USA; Department of Neurology, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd., Portland, OR 97239, USA.
Estrogen protects against multiple sclerosis relapses by boosting regulatory B cells and M2 macrophages/microglia. This creates a feedback loop enhancing neuroprotection during experimental autoimmune encephalomyelitis.
Area of Science:
- Neuroimmunology
- Endocrinology
- Cellular Biology
Background:
- Sex hormones like estrogen may prevent multiple sclerosis relapses during pregnancy.
- Regulatory B cells are vital for estrogen-mediated protection in experimental autoimmune encephalomyelitis (EAE).
Purpose of the Study:
- To investigate the role of estrogen in inducing regulatory B cells and M2 macrophages/microglia in EAE.
- To elucidate the interaction between M2 macrophages/microglia and regulatory B cells in estrogen-mediated neuroprotection.
Main Methods:
- Treatment of EAE mice with estrogen.
- Analysis of immune cell populations in the spinal cord.
- In vitro co-culture of M2-polarized microglia with B cells.
Main Results:
- Estrogen treatment increased alternatively activated (M2) macrophages/microglia in the spinal cord of EAE mice.
- Estrogen elevated the frequency of regulatory B cells in the spinal cord.
- M2-polarized microglia promoted the induction of regulatory B cells in vitro.
Conclusions:
- Estrogen induces a neuroprotective regulatory feedback loop involving M2 macrophages/microglia and regulatory B cells.
- This interaction is crucial for estrogen-mediated protection against EAE.
- Findings suggest potential therapeutic strategies for multiple sclerosis.
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