File:Human stem cell pancreas implants 01.jpg: Difference between revisions
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Mouse implanted with SC-β cells encapsulated with TMTD alginate. Cell encapsulation overcomes the need for immunosuppression by protecting therapeutic tissues from rejection by the host immune system. The most common method for islet encapsulation therapy is the formulation of isolated islets into alginate microspheres. | Mouse implanted with SC-β cells encapsulated with TMTD alginate. Cell encapsulation overcomes the need for immunosuppression by protecting therapeutic tissues from rejection by the host immune system. The most common method for islet encapsulation therapy is the formulation of isolated islets into alginate microspheres. | ||
DAPI in blue; insulin (i) or NKX6.1 (j) in green; glucagon (i) or C-peptide (j) in red. Scale bars, 50 μm. | |||
:'''Links:''' [[Stem Cells]] | [[Endocrine - Pancreas Development]] | [[Template_talk:Main_Page_News#March|March 2016 News]] | :'''Links:''' [[Stem Cells]] | [[Endocrine - Pancreas Development]] | [[Template_talk:Main_Page_News#March|March 2016 News]] |
Latest revision as of 10:58, 9 March 2016
Human stem cell implants retrieved 174 days after implantation in Mouse
Mouse implanted with SC-β cells encapsulated with TMTD alginate. Cell encapsulation overcomes the need for immunosuppression by protecting therapeutic tissues from rejection by the host immune system. The most common method for islet encapsulation therapy is the formulation of isolated islets into alginate microspheres.
DAPI in blue; insulin (i) or NKX6.1 (j) in green; glucagon (i) or C-peptide (j) in red. Scale bars, 50 μm.
Reference
<pubmed>26808346</pubmed>
Copyright
Reprinted by permission from Macmillan Publishers Ltd: Nature Medicine (Nature Medicine 22, 306–311 (2016) doi:10.1038/nm.4030), copyright (2016)
Figure 3 panel I and J cropped and resized from original figure. Citation and PMID added.
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