3D cell culturing by magnetic levitation

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The Magnetic Levitation Method (MLM) is a technique for 3D cell culture. In this approach, cells are treated with magnetic nanoparticles and exposed to spatially varying magnetic fields produced by neodymium magnetic drivers. The process causes cells to levitate to the air/liquid interface within a standard petri dish. The magnetic nanoparticle assemblies consist of magnetic iron oxide nanoparticles, gold nanoparticles, and cell-adhesive peptide sequences.

This method can be applied to cultures ranging from 500 cells to millions of cells and is adaptable for use in single-dish systems as well as high-throughput, low-volume systems. Additionally, magnetized cells can be utilized as building blocks for magnetic 3D bioprinting.

Overview

3D cell culture methods have been developed to enable research into the behavior of cells in an environment that more accurately represents their interactions in vivo.

3D cell culturing by magnetic levitation uses biocompatible polymer-based reagents to deliver magnetic nanoparticles to individual cells so that an applied magnetic driver can levitate cells off the bottom of the cell culture dish and rapidly bring cells together near the air-liquid interface. This initiates cell-cell interactions in the absence of any artificial surface or matrix. Magnetic fields are designed to form 3D multicellular structures, including the expression of extracellular matrix proteins. The matrix, protein expression, and response to exogenous agents of resulting tissue show similarity to in-vivo results.

History

3D cell culturing by magnetic levitation method (MLM) was developed with collaboration between scientists at Rice University and University of Texas MD Anderson Cancer Center in 2008. 3D cell culturing technology was later licensed and commercialized by Nano3D Biosciences.

The magnetic levitation process

The figure on the right shows 3D cell culturing through magnetic levitation using one possible system. Letters on the figure refer to the following:

(A) A magnetic iron oxide nanoparticle assembly, known as the "nanoshuttle", is added and dispersed over cells, and the mixture is incubated.

(B) After incubation with the nanoshuttle, the cells are detached and transferred to a petri dish.

(D) The magnetic field causes cells to rise to the air–medium interface.

(E) Human umbilical vein endothelial cells (HUVEC) levitated for 60 minutes (left two images in E) and 4 hours (right two images in E) (scale bar: 50 μm).

The onset of cell-cell interaction takes place as soon as cells levitate, and 3D structures start to form. At 1 hour, the cells are still relatively dispersed, but they already show some signs of stretching. Formation of 3D structures is visible after 4 hours of levitation (arrows in E).

Protein expression

Distribution of N-cadherin (red) and nuclei (blue). Left: human brain cancer cells grown in a mouse brain (xenograft). Middle: brain cancer cells cultured by 3D magnetic levitation for 48 hours. Right: cells cultured on a 2D glass slide cover slip.

Patterns of protein expression in levitated cultures resemble the patterns observed in-vivo. For example, as shown in the figure on the right, N-cadherin expression in levitated human glioblastoma (GBM) cells was similar to that seen in human tumor xenografts grown in immunodeficient mice (comparing the left and middle images), while standard 2D culture showed much weaker expression that did not match xenograft distribution (comparing the left and right images). The transmembrane protein N-cadherin is often used as an indicator of in vivo-like tissue assembly in 3D culturing.

Referring to the figure, in the mouse and levitated culture (left and middle image), N-cadherin is clearly concentrated in the membrane, and also present in cytoplasm and cell junctions, whereas the 2D system (right image) shows N-cadherin in the cytoplasm and nucleus, but notably absent from the membrane.

Applications

An invasion assay of magnetically levitated multicellular spheroids. Fluorescence images of human GBM cells (green; GFP-expressing cells) and NHA (red; MCherry-labelled), cultured separately then magnetically guided together.

Co-culturing, magnetic manipulation, and invasion assays

One of the challenges of in vitro modelling of complex tissues is the difficulty of co-culturing different cell types. Co-culturing of different cell types can be achieved at the onset of levitation, either by mixing different cell types before levitation, or by magnetically guiding 3D cultures in an invasion assay format.

Co-culturing in a realistic tissue architecture is important for accurately modeling in vivo conditions, such as increasing the accuracy of cellular assays, as shown in the figure on the right. In the figure, the human GBM cells and normal human astrocytes (NHA) are cultured separately and then magnetically guided together (left, time 0). Invasion of GBM into NHA in 3D culture provides an assay for basic cancer biology and drug screening (right, 12h to 252h).

Vascular simulation with stem cells

By facilitating the assembly of different populations of cells using the MLM, consistent generation of organoids, termed adipospheres, capable of simulating the complex intercellular interactions of endogenous white adipose tissue (WAT) can be achieved.

Co-culturing 3T3-L1 preadipocytes in a 3D space with murine endothelial bEND.3 cells can create a vascular-like network assembly with concomitant lipogenesis in perivascular cells (refer to the attached figure).

In addition to cell lines, organogenesis of white adipose tissue (WAT) can be simulated from primary cells.

Adipocyte-depleted stromal vascular fraction (SVF) containing adipose stromal cells (ASC), endothelial cells, and infiltrating leukocytes derived from mouse WAT were cultured in 3D. This revealed organoids striking in hierarchical organization with distinct capsules and internal large vessel-like structures lined with endothelial cells, as well as perivascular localization of ASC.

Upon adipogenesis induction of either 3T3-L1 adipospheres or adipospheres derived from SVF, the cells efficiently formed large lipid droplets typical of white adipocytes in vivo, whereas only smaller lipid droplet formation is achievable in 2D. This indicates intercellular signaling that better recapitulates WAT organogenesis.

This MLM for 3D co-culturing creates a liposphere appropriate for WAT modeling ex vivo and provides a new platform for functional screens to identify molecules bioactive toward individual adipose cell populations. It can also be adopted for WAT transplantation applications and aid other approaches to WAT-based cell therapy.

Organized co-culturing to create in vivo-like tissue

The use of additional manipulation tools may be needed to organize 3D co-cultures into a configuration similar enough to native tissue architecture.

Endothelial cells (PEC), smooth muscle cells (SMC), fibroblasts (PF), and epithelial cells (EpiC) cultured through magnetic levitation can be sequentially layered in a drag-and-drop manner to create bronchioles that maintain phenotype and induce extracellular matrix formation.

Cell types cultured

Listed below are the cell types (primary and cell lines) that have been successfully cultured by the magnetic levitation method.

Cells	Cell line	Organism	Organ tissue	Image
Murine endothelial	Cell line	Mouse	Vessel
Murine adipocyte	Cell line	Mouse	Adipose	Adipocytes cultured by MLM acquire in vivo morphology in adipospheres.
Rattus norvegicus hepatoma	Cell line	Rat	Liver	Hepatoma cultured by MLM for different cell numbers at 24 hours.
Human pulmonary fibroblasts (HPF)	Primary	Human	Lung	Primary pulmonary fibroblasts cultured by MLM compared to in vivo.
Pulmonary endothelial (HPMEC)	Primary	Human	Lung
Small airway epithelial (HSAEpiC)	Primary	Human	Lung	Primary small airway epithelial cells cultured by MLM compared to in vivo.
Bronchial epithelial	Primary	Human	Lung
Human alveolar adenocarcinoma	A549	Human	Lung	Human alveolar adenocarcinoma cell line - A549 cultured by MLM at different time points and cell numbers. Immunohistochemistry (IHC) reveals epithelial markers on A549 after culturing in 3D with the MLM.
Type II alveolar	Primary	Human	Lung
Human tracheal smooth muscle cells (HTSMCs)	Primary	Human	Lung	HTSMCs cultured by MLM with IHC staining.
Human mesenchymal stem cells (HMSCs)	Primary	Human	Bone marrow	HMSCs cultured by MLM.
Human bone marrow endothelial cells (HBMECs)	Primary	Human	Bone marrow
Dental pulp stem cells (DPSCs)	Primary	Human		Dental pulp cultured by MLM (3D vs. 2D) - 5 days.
Human umbilical vein endothelial cells (HUVECs)	Primary	Human		HUVECs cultured by MLM in 24 Well format.
Murine chondrocytes	Primary	Mouse	Bone	Chondrocytes cultured in 3D by MLM at different time points.
Murine adipose tissue	Primary	Mouse		Primary WAT cells cultured by MLM assemble into vascularized adipospheres.
Heart valve endothelial	Primary	Porcine
Pre-adipocytes fibroblasts	3T3	Mouse
Neural stem cells	C17.2	Mouse	Brain	Levitating neural stem cells cultured by MLM.
Human embryonic kidney cells	HEK293	Human	Kidney	HEK 293 cultured by MLM and tested with ibuprofen using bioassay.
]	B16	Mouse	Skin
Astrocytes	NHA	Human	Brain	Astrocyte and glioblastoma invasion assay performed after 3D culturing by MLM.
Glioblastomas	LN229	Human	Brain	Glioblastoma cultured with Bio-Assembler vs. Matrigel at 24 hours.
T-cells and antigen presenting cells		Human
Mammary epithelial	MCF10A	Human	Breast	Bio-Assembler vs. Matrigel with human mammary epithelial cells.
Breast cancer	MDA231	Human	Breast
Osteosarcoma	MG63	Human	Bone

References

Haisler, William L.; Timm, David M.; Gage, Jacob A.; Tseng, Hubert; Killian, T. C.; Souza, Glauco R. (October 2013). "Three-dimensional cell culturing by magnetic levitation". Nature Protocols. 8 (10): 1940–1949. doi:10.1038/nprot.2013.125. ISSN 1750-2799.
^ Souza, G. R. et al. Three-dimensional Tissue Culture Based on Magnetic Cell Levitation. Nature Nanotechnol.5, 291-296, doi:10.1038/nnano.2010.23 (2010).
^ Molina, J., Hayashi, Y., Stephens, C. & Georgescu, M.-M. Invasive glioblastoma cells acquire stemness and increased Akt activation. Neoplasia12, 453-463 (2010).
"Bio-Assembling in 3-D with Magnetic Levitation - Technology Review." Technology Review. N.p., n.d. Web. 20 Aug. 2012. <http://www.technologyreview.com/view/426363/bio-assembling-in-3-d-with-magnetic-levitation/>.
"N3D Biosciences, Inc. » ABOUT US." N3D Biosciences, Inc. » ABOUT US. N.p., n.d. Web. 20 Aug. 2012. <http://www.n3dbio.com/about/ Archived 2013-12-14 at the Wayback Machine>.
^ Daquinag, A. C., Souza, G. R., Kolonin, M. G. Adipose Tissue Engineering in Three-Dimensional Levitation Tissue Culture System Based on Magnetic Nanoparticles. Tissue Eng. Part C. -Not available-, ahead of print. doi:10.1089/ten.tec.2012.0198 (2012).
^ Tseng, H., Gage, J. A., Raphael, R., Moore, R. H., Killian, T. C., Grande-Allen, K. J., Souza, G. R. Assembly of a three-dimensional multitype bronchiole co-culture model using magnetic levitation. Tissue Eng. Part C. -Not available-, ahead of print. doi:10.1089/ten.TEC.2012.0157 (2013)
Jeong, Yun Gyu; Lee, Jin Sil; Shim, Jae Kwon; Hur, Won (December 2016). "A scaffold-free surface culture of B16F10 murine melanoma cells based on magnetic levitation". Cytotechnology. 68 (6): 2323–2334. doi:10.1007/s10616-016-0026-7. ISSN 0920-9069. PMC 5101302. PMID 27670438.

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