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新型三维巨噬细胞球体模型揭示免疫机械应力与机械免疫反应的相互调节。

Novel 3-D macrophage spheroid model reveals reciprocal regulation of immunomechanical stress and mechano-immunological response.

作者信息

Burchett Alice, Siri Saeed, Li Jun, Lu Xin, Datta Meenal

机构信息

Department of Aerospace and Mechanical Engineering, University of Notre Dame, IN, USA.

Department of Applied and Computational Mathematics and Statistics, University of Notre Dame, IN, USA.

出版信息

bioRxiv. 2024 Feb 17:2024.02.14.580327. doi: 10.1101/2024.02.14.580327.


DOI:10.1101/2024.02.14.580327
PMID:38405787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10888788/
Abstract

PURPOSE: In many diseases, an overabundance of macrophages contributes to adverse outcomes. While numerous studies have compared macrophage phenotype after mechanical stimulation or with varying local stiffness, it is unclear if and how macrophages themselves contribute to mechanical forces in their microenvironment. METHODS: Raw 264.7 murine macrophages were embedded in a confining agarose gel, where they proliferated to form spheroids over time. Gels were synthesized at various concentrations to tune the stiffness and treated with various growth supplements to promote macrophage polarization. The spheroids were then analyzed by immunofluorescent staining and qPCR for markers of proliferation, mechanosensory channels, and polarization. Finally, spheroid geometries were used to computationally model the strain generated in the agarose by macrophage spheroid growth. RESULTS: Macrophages form spheroids and generate growth-induced mechanical forces (i.e., solid stress) within confining agarose gels, which can be maintained for at least 16 days in culture. Increasing agarose concentration restricts spheroid expansion, promotes discoid geometries, limits gel deformation, and induces an increase in iNOS expression. LPS stimulation increases spheroid growth, though this effect is reversed with the addition of IFN-γ. Ki67 expression decreases with increasing agarose concentration, in line with the growth measurements. CONCLUSIONS: Macrophages alone both respond to and generate solid stress. Understanding how macrophage generation of growth-induced solid stress responds to different environmental conditions will help to inform treatment strategies for the plethora of diseases that involve macrophage accumulation.

摘要

目的:在许多疾病中,巨噬细胞过多会导致不良后果。虽然众多研究比较了机械刺激后或在不同局部硬度条件下的巨噬细胞表型,但尚不清楚巨噬细胞自身是否以及如何在其微环境中产生机械力。 方法:将Raw 264.7小鼠巨噬细胞包埋在封闭的琼脂糖凝胶中,随着时间推移它们会增殖形成球体。合成不同浓度的凝胶以调节硬度,并用各种生长补充剂处理以促进巨噬细胞极化。然后通过免疫荧光染色和qPCR分析球体中增殖、机械传感通道和极化的标志物。最后,利用球体几何形状对巨噬细胞球体生长在琼脂糖中产生的应变进行计算建模。 结果:巨噬细胞形成球体,并在封闭的琼脂糖凝胶中产生生长诱导的机械力(即固体应力),这种力在培养中可维持至少16天。增加琼脂糖浓度会限制球体扩张,促进盘状几何形状,限制凝胶变形,并诱导诱导型一氧化氮合酶(iNOS)表达增加。脂多糖(LPS)刺激会增加球体生长,不过添加γ干扰素(IFN-γ)后这种效应会逆转。Ki67表达随琼脂糖浓度增加而降低,与生长测量结果一致。 结论:仅巨噬细胞就能对固体应力做出反应并产生固体应力。了解巨噬细胞产生的生长诱导固体应力如何对不同环境条件做出反应,将有助于为涉及巨噬细胞积聚的众多疾病制定治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/058569bfa824/nihpp-2024.02.14.580327v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/86701f775fb9/nihpp-2024.02.14.580327v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/1234262770ab/nihpp-2024.02.14.580327v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/87e9ddacac85/nihpp-2024.02.14.580327v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/987f01b10c6d/nihpp-2024.02.14.580327v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/058569bfa824/nihpp-2024.02.14.580327v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/86701f775fb9/nihpp-2024.02.14.580327v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/1234262770ab/nihpp-2024.02.14.580327v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/87e9ddacac85/nihpp-2024.02.14.580327v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/987f01b10c6d/nihpp-2024.02.14.580327v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f685/10888788/058569bfa824/nihpp-2024.02.14.580327v1-f0005.jpg

相似文献

[1]
Novel 3-D macrophage spheroid model reveals reciprocal regulation of immunomechanical stress and mechano-immunological response.

bioRxiv. 2024-2-17

[2]
Novel 3-D Macrophage Spheroid Model Reveals Reciprocal Regulation of Immunomechanical Stress and Mechano-Immunological Response.

Cell Mol Bioeng. 2024-10-14

[3]
Mimicking the tumor microenvironment to regulate macrophage phenotype and assessing chemotherapeutic efficacy in embedded cancer cell/macrophage spheroid models.

Acta Biomater. 2017-3-1

[4]
Macrophage infiltration in 3D cancer spheroids to recapitulate the TME and unveil interactions within cancer cells and macrophages to modulate chemotherapeutic drug efficacy.

BMC Cancer. 2023-12-7

[5]
Micro-environmental mechanical stress controls tumor spheroid size and morphology by suppressing proliferation and inducing apoptosis in cancer cells.

PLoS One. 2009

[6]
Solid stress facilitates spheroid formation: potential involvement of hyaluronan.

Br J Cancer. 2002-3-18

[7]
Murine macrophage-based iNos reporter reveals polarization and reprogramming in the context of breast cancer.

Front Oncol. 2023-4-5

[8]
[Effect of Galectin-9/Tim-3 pathway on the polarization of M1/M2 subtype in murine macrophages induced by lipopolysaccharide].

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2018-9

[9]
Effect of Compressive Stress in Tumor Microenvironment on Malignant Tumor Spheroid Invasion Process.

Int J Mol Sci. 2022-6-25

[10]
Human fibroblast-macrophage tissue spheroids demonstrate ratio-dependent fibrotic activity for in vitro fibrogenesis model development.

Biomater Sci. 2020-3-31

本文引用的文献

[1]
Evidence and therapeutic implications of biomechanically regulated immunosurveillance in cancer and other diseases.

Nat Nanotechnol. 2024-3

[2]
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Drug Resist Updat. 2024-3

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Curr Opin Cell Biol. 2024-2

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Basic Res Cardiol. 2024-2

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Cell Metab. 2024-1-2

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Macrophage states: there's a method in the madness.

Trends Immunol. 2023-12

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Neurol Int. 2023-4-23

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Proc Natl Acad Sci U S A. 2023-2-7

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Cell. 2022-11-10

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Force- and cell state-dependent recruitment of Piezo1 drives focal adhesion dynamics and calcium entry.

Sci Adv. 2022-11-11

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