Se requiere una suscripción a JoVE para ver este contenido. Inicie sesión o comience su prueba gratuita.
Deriving enteric nervous system (ENS) lineages from human pluripotent stem cells (hPSC) provides a scalable source of cells to study ENS development and disease, and to use in regenerative medicine. Here, a detailed in vitro protocol to derive enteric neurons from hPSCs using chemically defined culture conditions is presented.
The human enteric nervous system, ENS, is a large network of glial and neuronal cell types with remarkable neurotransmitter diversity. The ENS controls bowel motility, enzyme secretion, and nutrient absorption and interacts with the immune system and the gut microbiome. Consequently, developmental and acquired defects of the ENS are responsible for many human diseases and may contribute to symptoms of Parkinson's disease. Limitations in animal model systems and access to primary tissue pose significant experimental challenges in studies of the human ENS. Here, a detailed protocol is presented for effective in vitro derivation of the ENS lineages from human pluripotent stem cells, hPSC, using defined culture conditions. Our protocol begins with directed differentiation of hPSCs to enteric neural crest cells within 15 days and yields diverse subtypes of functional enteric neurons within 30 days. This platform provides a scalable resource for developmental studies, disease modeling, drug discovery, and regenerative applications.
The enteric nervous system (ENS) is the largest component of the peripheral nervous system. The ENS contains more than 400 million neurons that are located within the GI tract and control nearly all functions of the gut1. Molecular understanding of the ENS development and function and its defects in enteric neuropathies requires access to a reliable and authentic source of enteric neurons. Access to human primary tissue is limited, and animal models fail to recapitulate key disease phenotypes in many enteric neuropathies. Human pluripotent stem cell (hPSC) technology has proven exceedingly beneficial in providing an unlimited source of desired ....
1. Media preparation
NOTE: Concentrations mentioned throughout the protocol are final concentrations of the media components. Prepare all media under sterile conditions in a laminar flow hood, and store at 4 °C in the dark. Use within 2 weeks.
This protocol provides a method to derive enteric neural crest and enteric neurons from hPSCs using chemically defined culture conditions (Figure 1A-B). Generating high-quality neurons depends on an efficient enteric neural crest induction step. This can be visually assessed by checking the morphology of the free-floating spheres that should look round with smooth surfaces with a size of approximately 0.1 - 0.4 mm as seen in Figure 1C. These sph.......
The differentiation protocol described here provides a robust in vitro method to obtain enteric neurons from hPSCs within 30-40 days (Figure 1E) and enteric glia expressing glial fibrillary acidic protein, GFAP, and SOX10 in older cultures (> day 55)13,14,19,22. These neurons and glia are induced by stepwise differentiation of hPSCs into vagal and ente.......
The work was supported by grants from UCSF Program for Breakthrough Biomedical Research and Sandler Foundation, March of Dimes grant no. 1-FY18-394 and 1DP2NS116769-01, the NIH Director's New Innovator Award (DP2NS116769) to F.F. and the National Institute of Diabetes and Digestive and Kidney Diseases (R01DK121169) to F.F., H.M. is supported by Larry L. Hillblom Foundation postdoctoral fellowship, NIH T32-DK007418 fellowship and UCSF Program for Breakthrough Biomedical Research independent postdoctoral fellowship.
....Name | Company | Catalog Number | Comments |
Ascorbic acid | Sigma-Aldrich | A5960 | |
B27 supplement (serum free, minus vitamin A) | Gibco | 12587-010 | |
Basement membrane matrix, Geltrex | Gibco | A14133-2 | |
BMP4 | R&D systems | 314-BP | |
Cell culture centrifuge | Eppendorf, model no. 5810R | 02262501 | |
Cell detachment solution, Accutase | Stemcell Technologies | 07920 | |
CHIR99021 | Tocris | 4423 | |
Conical tubes | USA scientific | 1475-0511, 1500-1211 | |
Differentiation base medium, Essential 6 | Life Technologies | A1516401 | |
DMEM/F-12 no glutamine | Life Technologies | 21331020 | |
EDTA | Corning | MT-46034CI | |
Feeder-free hPSC maintenance medium, Essential 8 Flex Medium Kit | Life Technologies | A2858501 | |
FGF2 | R&D systems | 233-FB/CF | |
Fibronectin | Corning | 356008 | |
GDNF | Peprotech | 450-10 | |
Hemocytometer | Hausser Scientific | 1475 | |
Human pluripotent stem cells, H9 ESC | WiCell | RRID: CVCL_1240 | |
Incubator with controlled humidity, temperature and CO2 | Thermo Fisher Scientific | Herralcell 150i | |
Inverted microscope | Thermo Fisher Scientific | EVOS FL | |
Laminar flow hood | Thermo Fisher Scientific | 1300 series class II, type A2 | |
Laminin | Cultrex | 3400-010 | |
L-glutamine supplement, Glutagro | Corning | 25-015-CI | |
MEM NEAAs | Corning | 25-025-CI | |
Multiwell plates, Falcon | BD | 353934, 353075 | |
N-2 Supplement | CTS | A1370701 | |
Neurobasal Medium | Life Technologies | 21103049 | |
PBS (Ca and Mg free) | Life Technologies | 10010023 | |
Pipette filler | Eppendorf | Z768715-1EA | |
Pipette tips | USA scientific | 1111-2830 | |
Pipettes | Fisherbrand | 13-678-11E, 13-678-11F | |
PO | Sigma-Aldrich | P3655 | |
polymer coverslip bottom imaging plates, ibidi | ibidi | 81156 | |
RA | Sigma-Aldrich | R2625 | |
SB431542 | R&D systems | 1614 | |
Trypan blue stain, 0.4% | Thermo Fisher Scientific | 15250-061 | |
Ultra-low attachment plates | Fisher Scientific | 07-200-601 | |
Y-27632 dihydrochloride | R&D systems | 1254 |
Explore More Articles
This article has been published
Video Coming Soon
ACERCA DE JoVE
Copyright © 2025 MyJoVE Corporation. Todos los derechos reservados