Premium
Induction of early neural precursors and derivation of tripotent neural stem cells from human pluripotent stem cells under xeno‐free conditions
Author(s) -
Nguyen Hal X.,
Nekanti Usha,
Haus Daniel L.,
Funes Gabrielle,
Moreno Denisse,
Kamei Noriko,
Cummings Brian J.,
Anderson Aileen J.
Publication year - 2014
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.23604
Subject(s) - biology , embryonic stem cell , induced pluripotent stem cell , microbiology and biotechnology , neural stem cell , kosr , neurosphere , stem cell , regenerative medicine , homeobox protein nanog , adult stem cell , genetics , gene
Human embryonic stem cells (hESC) and induced pluripotent stem cells (hiPSC) can differentiate into many cell types and are important for regenerative medicine; however, further work is needed to reliably differentiate hESC and hiPSC into neural‐restricted multipotent derivatives or specialized cell types under conditions that are free from animal products. Toward this goal, we tested the transition of hESC and hiPSC lines onto xeno‐free (XF) / feeder‐free conditions and evaluated XF substrate preference, pluripotency, and karyotype. Critically, XF transitioned H9 hESC, Shef4 hESC, and iPS6‐9 retained pluripotency (Oct‐4 and NANOG), proliferation (MKI67 and PCNA), and normal karyotype. Subsequently, XF transitioned hESC and hiPSC were induced with epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) to generate neuralized spheres containing primitive neural precursors, which could differentiate into astrocytes and neurons, but not oligoprogenitors. Further neuralization of spheres via LIF supplementation and attachment selection on CELLstart substrate generated adherent human neural stem cells (hNSC) with normal karyotype and high proliferation potential under XF conditions. Interestingly, adherent hNSC derived from H9, Shef4, and iPS6‐9 differentiated into significant numbers of O4+ oligoprogenitors (∼20–30%) with robust proliferation; however, very few GalC+ cells were observed (∼2–4%), indicative of early oligodendrocytic lineage commitment. Overall, these data demonstrate the transition of multiple hESC and hiPSC lines onto XF substrate and media conditions, and a reproducible neuralization method that generated neural derivatives with multipotent cell fate potential and normal karyotype. J. Comp. Neurol. 522:2767–2783, 2014. © 2014 Wiley Periodicals, Inc.