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TLR7 modulates extramedullary splenic erythropoiesis in P. yoelii NSM-infected mice through the regulation of iron metabolism of macrophages with IFN-γ

Splenomegaly is a prominent clinical manifestation of malaria and the causes remain incompletely clear. Anemia is induced in malaria and extramedullary splenic erythropoiesis is compensation for the loss of erythrocytes. However, the regulation of extramedullary splenic erythropoiesis in malaria is...

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Published in:Frontiers in immunology 2023-04, Vol.14, p.1123074-1123074
Main Authors: Li, Jiajie, Liu, Lin, Xing, Junmin, Chen, Dianhui, Fang, Chao, Mo, Feng, Gong, Yumei, Tan, Zhengrong, Liang, Guikuan, Xiao, Wei, Tang, Shanni, Wei, Haixia, Zhao, Shan, Xie, Hongyan, Pan, Xingfei, Yin, Xiaomao, Huang, Jun
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creator Li, Jiajie
Liu, Lin
Xing, Junmin
Chen, Dianhui
Fang, Chao
Mo, Feng
Gong, Yumei
Tan, Zhengrong
Liang, Guikuan
Xiao, Wei
Tang, Shanni
Wei, Haixia
Zhao, Shan
Xie, Hongyan
Pan, Xingfei
Yin, Xiaomao
Huang, Jun
description Splenomegaly is a prominent clinical manifestation of malaria and the causes remain incompletely clear. Anemia is induced in malaria and extramedullary splenic erythropoiesis is compensation for the loss of erythrocytes. However, the regulation of extramedullary splenic erythropoiesis in malaria is unknown. An inflammatory response could facilitate extramedullary splenic erythropoiesis in the settings of infection and inflammation. Here, when mice were infected with rodent parasites, NSM, TLR7 expression in splenocytes was increased. To explore the roles of TLR7 in splenic erythropoiesis, we infected wild-type and C57BL/6 mice with NSM and found that the development of splenic erythroid progenitor cells was impeded in mice. Contrarily, the treatment of the TLR7 agonist, R848, promoted extramedullary splenic erythropoiesis in wild-type infected mice, which highlights the implication of TLR7 on splenic erythropoiesis. Then, we found that TLR7 promoted the production of IFN-γ that could enhance phagocytosis of infected erythrocytes by RAW264.7. After phagocytosis of infected erythrocytes, the iron metabolism of RAW264.7 was upregulated, evidenced by higher iron content and expression of and . Additionally, the neutralization of IFN-γ impeded the extramedullary splenic erythropoiesis modestly and reduced the iron accumulation in the spleen of infected mice. In conclusion, TLR7 promoted extramedullary splenic erythropoiesis in NSM-infected mice. TLR7 enhanced the production of IFN-γ, and IFN-γ promoted phagocytosis of infected erythrocytes and the iron metabolism of macrophages , which may be related to the regulation of extramedullary splenic erythropoiesis by TLR7.
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Anemia is induced in malaria and extramedullary splenic erythropoiesis is compensation for the loss of erythrocytes. However, the regulation of extramedullary splenic erythropoiesis in malaria is unknown. An inflammatory response could facilitate extramedullary splenic erythropoiesis in the settings of infection and inflammation. Here, when mice were infected with rodent parasites, NSM, TLR7 expression in splenocytes was increased. To explore the roles of TLR7 in splenic erythropoiesis, we infected wild-type and C57BL/6 mice with NSM and found that the development of splenic erythroid progenitor cells was impeded in mice. Contrarily, the treatment of the TLR7 agonist, R848, promoted extramedullary splenic erythropoiesis in wild-type infected mice, which highlights the implication of TLR7 on splenic erythropoiesis. Then, we found that TLR7 promoted the production of IFN-γ that could enhance phagocytosis of infected erythrocytes by RAW264.7. After phagocytosis of infected erythrocytes, the iron metabolism of RAW264.7 was upregulated, evidenced by higher iron content and expression of and . Additionally, the neutralization of IFN-γ impeded the extramedullary splenic erythropoiesis modestly and reduced the iron accumulation in the spleen of infected mice. In conclusion, TLR7 promoted extramedullary splenic erythropoiesis in NSM-infected mice. 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After phagocytosis of infected erythrocytes, the iron metabolism of RAW264.7 was upregulated, evidenced by higher iron content and expression of and . Additionally, the neutralization of IFN-γ impeded the extramedullary splenic erythropoiesis modestly and reduced the iron accumulation in the spleen of infected mice. In conclusion, TLR7 promoted extramedullary splenic erythropoiesis in NSM-infected mice. TLR7 enhanced the production of IFN-γ, and IFN-γ promoted phagocytosis of infected erythrocytes and the iron metabolism of macrophages , which may be related to the regulation of extramedullary splenic erythropoiesis by TLR7.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>37180169</pmid><doi>10.3389/fimmu.2023.1123074</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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source Open Access: PubMed Central
subjects Animals
Erythropoiesis
extramedullary splenic erythropoiesis
IFN-γ
Immunology
Interferon-gamma - therapeutic use
Iron - metabolism
macrophages
Macrophages - metabolism
Malaria
Mice
Mice, Inbred C57BL
Spleen - metabolism
TLR7
Toll-Like Receptor 7
title TLR7 modulates extramedullary splenic erythropoiesis in P. yoelii NSM-infected mice through the regulation of iron metabolism of macrophages with IFN-γ
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