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Generation of functionally active resident macrophages from adipose tissue by 3D cultures
by
Arnaud, Emmanuelle
, Arlat, Adèle
, Authier, Hélène
, Dray, Cédric
, Nakhle, Jean
, Monsarrat, Paul
, Coste, Agnès
, Ousset, Marielle
, Thomas, Miguel
, Renoud, Marie-Laure
, Fontaine, Jessica
, Cousin, Béatrice
, Casteilla, Louis
in
3D culture
/ Adipose tissue
/ Adipose Tissue - cytology
/ Animals
/ Antibodies
/ Body fat
/ Bone marrow
/ Cell culture
/ Cell Culture Techniques - methods
/ Cell Culture Techniques, Three Dimensional - methods
/ Cell Differentiation
/ Cells, Cultured
/ Colony-stimulating factor
/ Flow cytometry
/ Homeostasis
/ Immunology
/ Invoices
/ Macrophage colony-stimulating factor
/ macrophage subpopulation
/ Macrophages - immunology
/ Macrophages - metabolism
/ Metabolism
/ Mice
/ Mice, Inbred C57BL
/ Penicillin
/ Phagocytes
/ Phagocytosis
/ Phenotype
/ Physiology
/ resident macrophage
/ Roles
/ Software
/ Spheroids
/ Spheroids, Cellular - cytology
/ Stroma
2024
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Generation of functionally active resident macrophages from adipose tissue by 3D cultures
by
Arnaud, Emmanuelle
, Arlat, Adèle
, Authier, Hélène
, Dray, Cédric
, Nakhle, Jean
, Monsarrat, Paul
, Coste, Agnès
, Ousset, Marielle
, Thomas, Miguel
, Renoud, Marie-Laure
, Fontaine, Jessica
, Cousin, Béatrice
, Casteilla, Louis
in
3D culture
/ Adipose tissue
/ Adipose Tissue - cytology
/ Animals
/ Antibodies
/ Body fat
/ Bone marrow
/ Cell culture
/ Cell Culture Techniques - methods
/ Cell Culture Techniques, Three Dimensional - methods
/ Cell Differentiation
/ Cells, Cultured
/ Colony-stimulating factor
/ Flow cytometry
/ Homeostasis
/ Immunology
/ Invoices
/ Macrophage colony-stimulating factor
/ macrophage subpopulation
/ Macrophages - immunology
/ Macrophages - metabolism
/ Metabolism
/ Mice
/ Mice, Inbred C57BL
/ Penicillin
/ Phagocytes
/ Phagocytosis
/ Phenotype
/ Physiology
/ resident macrophage
/ Roles
/ Software
/ Spheroids
/ Spheroids, Cellular - cytology
/ Stroma
2024
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Generation of functionally active resident macrophages from adipose tissue by 3D cultures
by
Arnaud, Emmanuelle
, Arlat, Adèle
, Authier, Hélène
, Dray, Cédric
, Nakhle, Jean
, Monsarrat, Paul
, Coste, Agnès
, Ousset, Marielle
, Thomas, Miguel
, Renoud, Marie-Laure
, Fontaine, Jessica
, Cousin, Béatrice
, Casteilla, Louis
in
3D culture
/ Adipose tissue
/ Adipose Tissue - cytology
/ Animals
/ Antibodies
/ Body fat
/ Bone marrow
/ Cell culture
/ Cell Culture Techniques - methods
/ Cell Culture Techniques, Three Dimensional - methods
/ Cell Differentiation
/ Cells, Cultured
/ Colony-stimulating factor
/ Flow cytometry
/ Homeostasis
/ Immunology
/ Invoices
/ Macrophage colony-stimulating factor
/ macrophage subpopulation
/ Macrophages - immunology
/ Macrophages - metabolism
/ Metabolism
/ Mice
/ Mice, Inbred C57BL
/ Penicillin
/ Phagocytes
/ Phagocytosis
/ Phenotype
/ Physiology
/ resident macrophage
/ Roles
/ Software
/ Spheroids
/ Spheroids, Cellular - cytology
/ Stroma
2024
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Generation of functionally active resident macrophages from adipose tissue by 3D cultures
Journal Article
Generation of functionally active resident macrophages from adipose tissue by 3D cultures
2024
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Overview
Within adipose tissue (AT), different macrophage subsets have been described, which played pivotal and specific roles in upholding tissue homeostasis under both physiological and pathological conditions. Nonetheless, studying resident macrophages
poses challenges, as the isolation process and the culture for extended periods can alter their inherent properties.
Stroma-vascular cells isolated from murine subcutaneous AT were seeded on ultra-low adherent plates in the presence of macrophage colony-stimulating factor. After 4 days of culture, the cells spontaneously aggregate to form spheroids. A week later, macrophages begin to spread out of the spheroid and adhere to the culture plate.
This innovative three-dimensional (3D) culture method enables the generation of functional mature macrophages that present distinct genic and phenotypic characteristics compared to bone marrow-derived macrophages. They also show specific metabolic activity and polarization in response to stimulation, but similar phagocytic capacity. Additionally, based on single-cell analysis, AT-macrophages generated in 3D culture mirror the phenotypic and functional traits of
AT resident macrophages.
Our study describes a 3D
system for generating and culturing functional AT-resident macrophages, without the need for cell sorting. This system thus stands as a valuable resource for exploring the differentiation and function of AT-macrophages
in diverse physiological and pathological contexts.
Publisher
Frontiers Media SA,Frontiers Media S.A
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