Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published March 15, 2019 | Supplemental Material + Submitted + Published
Journal Article Open

Maintaining multipotent trunk neural crest stem cells as self-renewing crestospheres

Abstract

Neural crest cells have broad migratory and differentiative ability that differs according to their axial level of origin. However, their transient nature has limited understanding of their stem cell and self-renewal properties. While an in vitro culture method has made it possible to maintain cranial neural crest cells as self-renewing multipotent crestospheres (Kerosuo et al., 2015), these same conditions failed to preserve trunk neural crest in a stem-like state. Here we optimize culture conditions for maintenance of avian trunk crestospheres, comprised of both neural crest stem and progenitor cells. Our trunk-derived crestospheres are multipotent and display self-renewal capacity over several weeks. Trunk crestospheres display elevated expression of neural crest cell markers as compared to those characteristic of ventrolateral neural tube or mesodermal fates. Moreover, trunk crestospheres express increased levels of trunk neural crest-enriched markers as compared to cranial crestospheres. Finally, we use lentiviral transduction as a tool to manipulate gene expression in trunk crestospheres. Taken together, this method enables long-term in vitro maintenance and manipulation of multipotent trunk neural crest cells in a premigratory stem or early progenitor state. Trunk crestospheres are a valuable resource for probing mechanisms underlying neural crest stemness and lineage decisions as well as accompanying diseases.

Additional Information

© 2019 Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/). Received 17 August 2018, Revised 9 January 2019, Accepted 9 January 2019, Available online 18 January 2019. We would like to thank Elina Fredlund for technical assistance. This work was supported by the Swedish Childhood Cancer Fund, Sweden (to SM), the Mary Bevé Foundation (to SM), Magnus Bergvall Foundation, Sweden (to SM), the Thelma Zoéga Foundation, Sweden (to SM), Hans von Foundation (to SM), the Royal Physiographic Society in Lund, Sweden (to SM), the Gyllenstiernska Krapperup Foundation, Sweden (to SM), Gunnar Nilsson Cancer Foundation, Sweden (to SM), NIH, United States, Ruth L. Kirschstein NRSA F32HD087026 (to EK), NIH R01DE024157 (to MB), the Academy of Finland, Finland (to LK), Sigrid Jusélius Foundation, Finland (to LK), and in part by the Division of Intramural Research of the National Institute of Dental and Craniofacial Research at the National Institutes of Health, Department of Health and Human Services.

Attached Files

Published - 1-s2.0-S001216061830558X-main.pdf

Submitted - 391599.full.pdf

Supplemental Material - 1-s2.0-S001216061830558X-mmc1.docx

Supplemental Material - 1-s2.0-S001216061830558X-mmc2.pdf

Supplemental Material - 1-s2.0-S001216061830558X-mmc3.pdf

Files

1-s2.0-S001216061830558X-main.pdf
Files (12.7 MB)
Name Size Download all
md5:d5cf8748f9ad26b081933b7a92026bb2
2.1 MB Preview Download
md5:d569792f7c2c2b664836e6d40f9bc89f
37.2 kB Preview Download
md5:1915e23cee3d3a106a6f0184b08036af
87.2 kB Preview Download
md5:0fa2f047163e89df25673b19189ef1d4
26.7 kB Download
md5:b67ca43c06f09e871124f7c5d1bef24b
10.5 MB Preview Download

Additional details

Created:
August 22, 2023
Modified:
October 23, 2023