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Published on: March 30, 2018
Platelet-Derived Growth Factor-D Activates Complement System to Propagate Macrophage Polarization and
Zhen Xiong1, Qianqian Wang1, Wanhong Li1
1State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
Platelet-derived growth factor-D (PDGF-D) activates complement pathways, enhancing immune responses and macrophage polarization. Targeting PDGF-D and complement may treat neovascular diseases.
Area of Science:
- Immunology
- Complement System Biology
- Ophthalmology
Background:
- Platelet-derived growth factor-D (PDGF-D) is prevalent in immune cells, but its immune function is largely unknown.
- Understanding PDGF-D's role is crucial for immune system research.
Purpose of the Study:
- To elucidate the function of PDGF-D in the immune system.
- To investigate PDGF-D's role in macrophage polarization and associated inflammatory diseases.
- To explore therapeutic strategies targeting PDGF-D and the complement system.
Main Methods:
- Investigated PDGF-D's effect on classical and alternative complement pathways.
- Assessed PDGF-D-induced chemokine and cytokine production.
- Analyzed macrophage polarization.
- Utilized C3a receptor antagonist SB290157 to study neuroinflammation and choroidal neovascularization.
Main Results:
- PDGF-D activates both classical and alternative complement pathways.
- PDGF-D significantly increases chemokine and cytokine responses, promoting macrophage polarization.
- SB290157 treatment reduced PDGF-D-induced neuroinflammation by inhibiting macrophage polarization.
- Targeting the complement C3a receptor with SB290157 inhibited pathological choroidal neovascularization.
Conclusions:
- PDGF-D plays a novel role in activating complement pathways and modulating immune responses.
- PDGF-D-induced macrophage polarization contributes to neuroinflammation and neovascular diseases.
- Therapeutic strategies targeting both PDGF-D and the complement system show promise for treating neovascular diseases.
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