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Species-specific maturation profiles of human, chimpanzee and bonobo neural cells.

Maria C Marchetto | Branka Hrvoj-Mihic | Bilal E Kerman | Diana X Yu | Krishna C Vadodaria | Sara B Linker | Iñigo Narvaiza | Renata Santos | Ahmet M Denli | Ana Pd Mendes | Ruth Oefner | Jonathan Cook | Lauren McHenry | Jaeson M Grasmick | Kelly Heard | Callie Fredlender | Lynne Randolph-Moore | Rijul Kshirsagar | Rea Xenitopoulos | Grace Chou | Nasun Hah | Alysson R Muotri | Krishnan Padmanabhan | Katerina Semendeferi | Fred H Gage
eLife | 2019

Comparative analyses of neuronal phenotypes in closely related species can shed light on neuronal changes occurring during evolution. The study of post-mortem brains of nonhuman primates (NHPs) has been limited and often does not recapitulate important species-specific developmental hallmarks. We utilize induced pluripotent stem cell (iPSC) technology to investigate the development of cortical pyramidal neurons following migration and maturation of cells grafted in the developing mouse cortex. Our results show differential migration patterns in human neural progenitor cells compared to those of chimpanzees and bonobos both in vitro and in vivo, suggesting heterochronic changes in human neurons. The strategy proposed here lays the groundwork for further comparative analyses between humans and NHPs and opens new avenues for understanding the differences in the neural underpinnings of cognition and neurological disease susceptibility between species.

Pubmed ID: 30730291

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NIMH NIH HHS, United States
    Id: R01 MH095741
  • Agency: National Alliance for Research on Schizophrenia and Depression, International
    Id: Young Investigator award
  • Agency: NIH HHS, United States
    Id: DP2 OD006495
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH113924
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH103134
  • Agency: Salk Cancer Center, International
    Id: NCI P30 CA014195
  • Agency: NIMH NIH HHS, United States
    Id: K99 MH101634
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH100175
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH094753
  • Agency: NIMH NIH HHS, United States
    Id: R00 MH101634
  • Agency: NIH HHS, United States
    Id: Research Project Grant
  • Agency: California Institute for Regenerative Medicine, International
    Id: Research Grant
  • Agency: NIMH NIH HHS, United States
    Id: U19 MH107367
  • Agency: NIH HHS, United States
    Id: Pathway to independence award
  • Agency: Leona M. and Harry B. Helmsley Charitable Trust, International
    Id: Research Project Grant
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH088485

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