Cited by 46Cellular Mechanics and InteractionsCancer Cells and Metastasis3D Printing in Biomedical Research

Cell death and lumen formation in spheroids of MCF-7 cells

Amaral, Do Bussador Jônatas, Urabayashi, Shiniti Marcel, Machado‐Santelli, Maria Gláucia·2010·Cell Biology International

Abstract

3D (three-dimensional) cell culture permits a more integrated analysis of the relationship between cells, inserting them into a structure more closely resembling the cellular microenvironment in vivo. The development of in vitro parameters to approximate in vivo 3D cellular environments makes a less reductionist interpretation of cell biology possible. For breast cells, in vitro 3D culture has proven to be an important tool for the analysis of luminal morphogenesis. A greater understanding of this process is necessary because alterations in the lumen arrangement are associated with carcinogenesis. Following lumen formation in 3D cell culture using laser scanning confocal microscopy, we observed alterations in the arrangement of cytoskeletal components (F-actin and microtubules) and increasing levels of cell death associated with lumen formation. The formation of a polarized monolayer facing the lumen was characterized through 3D reconstructions and the use of TEM (transmission electron microscopy), and this process was found to occur through the gradual clearing of cells from the medullary region of the spheroids. This process was associated with different types of cell death, such as apoptosis, autophagy and entosis. The present study showed that changes in the extracellular matrix associated with long periods of time in 3D cell culture lead to the formation of a lumen in MCF-7 cell spheroids and that features of differentiation such as lumen and budding formation occur afte…

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Crossref · 10.1042/cbi20090024

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  • Electron microscopy, including scanning and transmission modalities, provides ultra-high-resolution imaging and remains valuable for evaluating cellular morphology, surface topology, and intercellular organization across spheroid layers.

    “Electron microscopy, including both scanning (SEM) and transmission (TEM) modalities, provides ultra-high-resolution imaging and remains a valuable tool for evaluating cellular morphology, surface topology, and intercellular organization across spheroid layers [245,256].”

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Authors
Amaral, D. B. J., Urabayashi, S. M., & Machado‐Santelli, M. G.
Venue
Cell Biology International
Publisher
Wiley
Published
2010-03
Volume
34
Issue
3
Pages
267-274
ISSN
  • 1065-6995 (ISSN-L)
  • 1095-8355
OpenAlex
W1484298894
Cited by
46
References
1
Citations by year
2026: 1 · 2025: 3 · 2024: 2 · 2023: 2 · 2022: 5 · 2021: 7 · 2020: 4 · 2019: 3 · 2018: 2 · 2017: 1 · 2016: 2 · 2015: 4 · 2014: 2 · 2013: 1 · 2012: 3
FWCI
1.03
Type
journal article
Language
en
Open access
closed
Locations
  • Cell Biology International (publishedVersion)
  • PubMed (publishedVersion)
  • Scientific Electronic Library Online (São Paulo Research Foundation, Latin American and Caribbean Center on Health Sciences Information, Conselho Nacional de Desenvolvimento Científico e Tecnológico) (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
  • Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
Keywords
lumen formation, MCF-7 cells, 3D cell culture, cell death, apoptosis, autophagy, entosis, F-actin, microtubules, cytoskeleton, extracellular matrix, cell differentiation
MeSH terms
Actins, Breast Neoplasms, Cell Differentiation, Cytoskeleton, Female, Humans, Microtubules, Morphogenesis, Tumor Cells, Cultured, Apoptosis, Spheroids, Cellular, Cell Culture Techniques, Cell Line, Tumor

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