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Role of IL-4 in bone marrow driven dysregulated angiogenesis and age-related macular degeneration.


ABSTRACT: Age-associated sterile inflammation can cause dysregulated choroidal neovascularization (CNV) as age-related macular degeneration (AMD). Intraocular fluid screening of 234 AMD patients identified high levels of IL-4. The purpose of this study was to determine the functional role of IL-4 in CNV formation using murine CNV model. Our results indicate that the IL-4/IL-4 receptors (IL4Rs) controlled tube formation and global proangiogenic responses of bone marrow cells. CCR2+ bone marrow cells were recruited to form very early CNV lesions. IL-4 rapidly induces CCL2, which enhances recruitment of CCR2+ bone marrow cells. This in vivo communication, like quorum-sensing, was followed by the induction of IL-4 by the bone marrow cells during the formation of mature CNVs. For CNV development, IL-4 in bone marrow cells are critically required, and IL-4 directly promotes CNV formation mainly by IL-4R. The IL-4/IL-4R? axis contributes to pathological angiogenesis through communications with bone marrow cells leading to retinal degeneration.

SUBMITTER: Baba T 

PROVIDER: S-EPMC7200155 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Role of IL-4 in bone marrow driven dysregulated angiogenesis and age-related macular degeneration.

Baba Takashi T   Miyazaki Dai D   Inata Kodai K   Uotani Ryu R   Miyake Hitomi H   Sasaki Shin-Ichi SI   Shimizu Yumiko Y   Inoue Yoshitsugu Y   Nakamura Kazuomi K  

eLife 20200505


Age-associated sterile inflammation can cause dysregulated choroidal neovascularization (CNV) as age-related macular degeneration (AMD). Intraocular fluid screening of 234 AMD patients identified high levels of IL-4. The purpose of this study was to determine the functional role of IL-4 in CNV formation using murine CNV model. Our results indicate that the IL-4/IL-4 receptors (IL4Rs) controlled tube formation and global proangiogenic responses of bone marrow cells. CCR2<sup>+</sup> bone marrow c  ...[more]

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