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Merck

Cerebral organoids model human brain development and microcephaly.

Nature (2013-09-03)
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, Daniel Wenzel, Louise S Bicknell, Matthew E Hurles, Tessa Homfray, Josef M Penninger, Andrew P Jackson, Juergen A Knoblich
要旨

The complexity of the human brain has made it difficult to study many brain disorders in model organisms, highlighting the need for an in vitro model of human brain development. Here we have developed a human pluripotent stem cell-derived three-dimensional organoid culture system, termed cerebral organoids, that develop various discrete, although interdependent, brain regions. These include a cerebral cortex containing progenitor populations that organize and produce mature cortical neuron subtypes. Furthermore, cerebral organoids are shown to recapitulate features of human cortical development, namely characteristic progenitor zone organization with abundant outer radial glial stem cells. Finally, we use RNA interference and patient-specific induced pluripotent stem cells to model microcephaly, a disorder that has been difficult to recapitulate in mice. We demonstrate premature neuronal differentiation in patient organoids, a defect that could help to explain the disease phenotype. Together, these data show that three-dimensional organoids can recapitulate development and disease even in this most complex human tissue.

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Sigma-Aldrich
抗Sox2抗体, Chemicon®, from rabbit
Sigma-Aldrich
抗ビンキュリン抗体、モウスモノクローナル, clone hVIN-1, purified from hybridoma cell culture
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抗リーリン抗体、a.a. 164-189 mreelin、クローン142, clone 142, Chemicon®, from mouse
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抗Prox1抗体、クローン4G10, clone 4G10, Chemicon®, from mouse
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Anti-TSH2 antibody produced in rabbit, affinity isolated antibody