4.8 Article

Three-Dimensional Culture Decreases the Angiogenic Ability of Mouse Macrophages

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FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.795066

关键词

3D culture; macrophage; angiogenesis; collagen microcarrier; VEGFA; ANG2

资金

  1. National Key R&D Program of China [2018YFC0114707]
  2. Key R&D Program of Shandong Province [2018GSF118047]
  3. Science and Technology Project of the Jilin Provincial Department of Science and Technology [20180201029YY]

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The study established a 3D culture system for macrophages using collagen microcarriers, finding that macrophages grown in 3D culture had significantly different morphology, arrangement, and angiogenic capabilities compared to those in 2D culture. Whole-transcriptome sequencing revealed significant gene expression differences, including downregulation of important angiogenic factors, and decreased expression of genes related to key angiogenic pathways in 3D-cultured macrophages.
Macrophages play important roles in angiogenesis; however, previous studies on macrophage angiogenesis have focused on traditional 2D cultures. In this study, we established a 3D culture system for macrophages using collagen microcarriers and assessed the effect of 3D culture on their angiogenic capabilities. Macrophages grown in 3D culture displayed a significantly different morphology and arrangement under electron microscopy compared to those grown in 2D culture. Tube formation assays and chick embryo chorioallantoic membrane assays further revealed that 3D-cultured macrophages were less angiogenic than those in 2D culture. Whole-transcriptome sequencing showed that nearly 40% of genes were significantly differently expressed, including nine important angiogenic factors of which seven had been downregulated. In addition, the expression of almost all genes related to two important angiogenic pathways was decreased in 3D-cultured macrophages, including the two key angiogenic factors, VEGFA and ANG2. Together, the findings of our study improve our understanding of angiogenesis and 3D macrophage culture in tissues, and provide new avenues and methods for future research on macrophages.

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