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Stem Cell Organoids

Realize Your Cells’ Potential.  Create Micro-tissues.

Scientists have mastered the art of chemical signaling in 2D culture to recapitulate disease and development.  However, it has become increasingly apparent that the emergence of more complex structures and micro-tissues requires mechanical signaling from a tissue-like, 3D environment[1],[2].

Recent examples include neuronal organoid development[3], optic cup morphogenesis[4], gut organoid development[6], and liver buds[7].  These “emergent micro-tissues” hold promise for both therapeutic applications as well as in vitro disease models.

3D culture is better for modeling development and disease compared to 2D because it creates a more realistic environment for cellular mechanisms that involve:

 

Cell-cell and cell-matrix adhesion[8]

Mechanical signaling[9]

Chemical and gas diffusion gradients[10]

Germ layer regulation and signaling[11]

Complex patterning[12]

Model Development and Disease with Cell-Mate3DTM

Culture cells in Cell-Mate3DTM and propagate in media of choice.  Cell-Mate3DTM is ideal for:

  • IPSCs
  • ES cells
  • MSCs
  • 3T3s, HEKs, etc.
  • Genetically modified cells
  • Co-cultures
  • In vivo Applications (Injectable)

Cell-Mate3DTM Has Advantages Over Other 3D Options Because It:

  • Exhibits tissue-like stiffness, mimicking the natural cell environment
  • Permits long-term 3D cultures without producing a necrotic core
  • Binds CD44 cell adhesion protein, allowing for cell-matrix interaction

Researchers benefit because Cell-Mate3DTM is:

  • Chemically defined
  • Injectable for use in animal models
  • Free of chemical and UV crosslinking
  • Efficient and easy to use

[1]Brendon M. Baker et al. Deconstructing the third dimension – how 3D culture microenvironments alter cellular cues. J Cell Sci 2012. 125(Pt 13):3015-3024.

[2] Marius Ader et al. Modeling human development in 3D culture. Curr Opin Cell Biol 2014. 31:23–28

[3]Lancaster MA et al.Cerebral organoids model human brain development and microcephaly. Nature 2013. 501(7467):373-379

[4] Mototsugu Eiraku et al. Self-organizing optic-cup morphogenesis in three-dimensional culture.  Nature 2011. 472(7341):51-56

[5] Tokushige Nakano et al. Self-Formation of Optic Cups and Storable Stratified Neural Retina from Human ESCs. Cell Stem Cell 2012. 10(6):771-785

[6] Spence et al.: Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro. Nature 2011. 470(7332):105-109.

[7] Takanori Takebe et al. Generation of a vascularized and functional human liver from an iPSC-derived organ bud transplant. Nat Protoc 2014. (2):396-409

[8] Oliver Zschenker et al. Genome-Wide Gene Expression Analysis in Cancer Cells Reveals 3D Growth to Affect ECM and Processes Associated with Cell Adhesion but Not DNA Repair. PLoS One 2012. 7(4):e34279

[9] Brendon M. Baker. Deconstructing the third dimension – how 3D culture microenvironments alter cellular cues. J Cell Sci. 2012. 125(Pt 13):3015-24.

[10] Brendon M. Baker et al. Deconstructing the third dimension – how 3D culture microenvironments alter cellular cues. J Cell Sci 2012. 125(Pt 13):3015-3024.

[11] Yeh-Chuin Poh. Generation of organized germ layers from a single mouse embryonic stem cell. Nat Commun. 2014. 5:4000.

[12] Koehler, K.R., et al., Generation of inner ear sensory epithelia from pluripotent stem cells in 3D culture. Nature. 2013. 500(7461):217-221

Analyze your Cell-Mate3D™ cultures using common laboratory techniques

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