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Hepatocyte-controlled availability of activated TGFb reprograms macrophage polarization affecting liver injury and regeneration

ChEBI2022-12-31 更新2026-07-12 收录

脏器免疫调控

巨噬细胞极化

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-11727 数据链接链接失效反馈

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资源简介：

Hepatocyte-controlled availability of activated TGFb reprograms macrophage polarization affecting liver injury and regeneration

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创建时间：

2022-12-31

巨噬细胞极化

免疫转录组

The goal of this study is to compare the gene expression profiles of two populations of human monocyte-derived macrophages (HMDMs) that were subjected to differentiation in either of two colony-stimul

NIAID Data Ecosystem70

Placental exosomes polarize human monocyte-derived macrophages to a decidual M2-like macrophage phenotype. Placental exosomes polarize human monocyte-derived macrophages to a decidual M2-like macrophage phenotype

外泌体免疫调控

巨噬细胞极化

Macrophages are abundant in uterine mucosa during the peri-implantation phase and early pregnancy. Decidual macrophages display dynamic changes alone with pregnancy progress: During the peri-implantat

NIAID Data Ecosystem30

Herpesvirus-encoded microRNA dysregulate M1 and M2 macrophage miRNA profiles

病毒miRNA调控

巨噬细胞极化

Primary human M1 and M2 macrophages were transfected with different human herpesvirus-derived viral miRNA and the impact on the cellular microRNAs was profiled using microarray. Viral miRNA-mediated i

NIAID Data Ecosystem20

Herpesvirus-encoded microRNA dysregulate M1 and M2 macrophage miRNA profiles. Herpesvirus-encoded microRNA dysregulate M1 and M2 macrophage miRNA profiles

病毒miRNA调控

巨噬细胞极化

NIAID Data Ecosystem40

Mus musculus Raw sequence reads. Mus musculus

缺血再灌注损伤

巨噬细胞极化

we performed RNA-Seq using separated macrophages from kidneys of WT and Lyz-TSC1cKO groups at 24h and 2 weeks after IRI to explore the mechanisms involved in macrophage polarization.

NIAID Data Ecosystem30

Hepatocyte-controlled availability of activated TGFb reprograms macrophage polarization affecting liver injury and regeneration

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