TY - JOUR
T1 - Deciphering the Proteome Dynamics during Development of Neurons Derived from Induced Pluripotent Stem Cells
AU - Varderidou-Minasian, Suzy
AU - Verheijen, Bert M.
AU - Schätzle, Philipp
AU - Hoogenraad, Casper C.
AU - Pasterkamp, R. Jeroen
AU - Altelaar, Maarten
PY - 2020/6/5
Y1 - 2020/6/5
N2 - Neuronal development is a complex multistep process that shapes neurons by progressing though several typical stages, including axon outgrowth, dendrite formation, and synaptogenesis. Knowledge of the mechanisms of neuronal development is mostly derived from the study of animal models. Advances in stem cell technology now enable us to generate neurons from human induced pluripotent stem cells (iPSCs). Here we provide a mass spectrometry-based quantitative proteomic signature of human iPSC-derived neurons, i.e., iPSC-derived induced glutamatergic neurons and iPSC-derived motor neurons, throughout neuronal differentiation. Tandem mass tag 10-plex labeling was carried out to perform proteomic profiling of cells at different time points. Our analysis reveals significant expression changes (FDR < 0.001) of several key proteins during the differentiation process, e.g., proteins involved in the Wnt and Notch signaling pathways. Overall, our data provide a rich resource of information on protein expression during human iPSC neuron differentiation.
AB - Neuronal development is a complex multistep process that shapes neurons by progressing though several typical stages, including axon outgrowth, dendrite formation, and synaptogenesis. Knowledge of the mechanisms of neuronal development is mostly derived from the study of animal models. Advances in stem cell technology now enable us to generate neurons from human induced pluripotent stem cells (iPSCs). Here we provide a mass spectrometry-based quantitative proteomic signature of human iPSC-derived neurons, i.e., iPSC-derived induced glutamatergic neurons and iPSC-derived motor neurons, throughout neuronal differentiation. Tandem mass tag 10-plex labeling was carried out to perform proteomic profiling of cells at different time points. Our analysis reveals significant expression changes (FDR < 0.001) of several key proteins during the differentiation process, e.g., proteins involved in the Wnt and Notch signaling pathways. Overall, our data provide a rich resource of information on protein expression during human iPSC neuron differentiation.
KW - human development
KW - iPSC
KW - mass spectrometry
KW - neuronal development
KW - neuronal differentiation
KW - neuroproteomics
KW - proteome
KW - quantitative proteomics
KW - tandem mass tags
KW - TMT 10-plex
UR - http://www.scopus.com/inward/record.url?scp=85086051119&partnerID=8YFLogxK
U2 - 10.1021/acs.jproteome.0c00070
DO - 10.1021/acs.jproteome.0c00070
M3 - Article
C2 - 32357013
AN - SCOPUS:85086051119
SN - 1535-3893
VL - 19
SP - 2391
EP - 2403
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 6
ER -