TY - JOUR
T1 - Wilms tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repair
AU - Lopez-Baez, Juan Carlos
AU - Simpson, Daniel J.
AU - Forero, Laura LLeras
AU - Zeng, Zhiqiang
AU - Brunsdon, Hannah
AU - Salzano, Angela
AU - Brombin, Alessandro
AU - Wyatt, Cameron
AU - Rybski, Witold
AU - Huitema, Leonie F.A.
AU - Dale, Rodney M.
AU - Kawakami, Koichi
AU - Englert, Christoph
AU - Chandra, Tamir
AU - Schulte-Merker, Stefan
AU - Hastie, Nicholas D.
AU - Patton, E. Elizabeth
N1 - Funding Information:
We thank staff at the MRC Human Genetics Unit for excellent support, including Craig Nicol and Connor Warnock for assistance with figure design, Elisabeth Freyer for FACS analysis, and the zebra- fish facility staff in Edinburgh and Utrecht for zebrafish husbandry. We thank Lee Murphy at the Edin- burgh Clinical Research Facility for excellent service and support, Jeanette Baran-Gale for important advice on the bioinformatics analysis, and Andrea Coates for critical reading of the manuscript. Medical Research Council MC_PC_U127585840 Juan Carlos Lopez-Baez Zhiqiang Zeng Alessandro Brombin Witold Rybski E Elizabeth Patton Medical Research Council MC_PC_U127527180 Juan Carlos Lopez-Baez Nicholas D Hastie Medical Research Council Doctoral Training Programme in Percision Medicine Daniel J Simpson H2020 European Research Council ZF-MEL-CHEMBIO - 648489 Hannah Brunsdon Alessandro Brombin E Elizabeth Patton Medical Research Council Discovery Award MC_PC_15075 Angela Salzano Melanoma Research Alliance 401181 Alessandro Brombin E Elizabeth Patton L’Oreal USA 401181 Alessandro Brombin E Elizabeth Patton Japan Society for the Promo- tion of Science 15H02370 Koichi Kawakami Japan Agency for Medical Re- search and Development National BioResource Project Koichi Kawakami Leibniz-Gemeinschaft Christoph Englert University Of Edinburgh Chancellor’s Fellowship Tamir Chandra Cells in Motion - Cluster of Excellence EXC 1003-CiM Stefan Schulte-Merker.
Publisher Copyright:
© Lopez-Baez et al.
PY - 2018/2/6
Y1 - 2018/2/6
N2 - Regenerative therapy for degenerative spine disorders requires the identification of cells that can slow down and possibly reverse degenerative processes. Here, we identify an unanticipated wound-specific notochord sheath cell subpopulation that expresses Wilms Tumor (WT) 1b following injury in zebrafish. We show that localized damage leads to Wt1b expression in sheath cells, and that wt1b+cells migrate into the wound to form a stopper-like structure, likely to maintain structural integrity. Wt1b+sheath cells are distinct in expressing cartilage and vacuolar genes, and in repressing a Wt1b-p53 transcriptional programme. At the wound, wt1b+and entpd5+ cells constitute separate, tightly-associated subpopulations. Surprisingly, wt1b expression at the site of injury is maintained even into adult stages in developing vertebrae, which form in an untypical manner via a cartilage intermediate. Given that notochord cells are retained in adult intervertebral discs, the identification of novel subpopulations may have important implications for regenerative spine disorder treatments.
AB - Regenerative therapy for degenerative spine disorders requires the identification of cells that can slow down and possibly reverse degenerative processes. Here, we identify an unanticipated wound-specific notochord sheath cell subpopulation that expresses Wilms Tumor (WT) 1b following injury in zebrafish. We show that localized damage leads to Wt1b expression in sheath cells, and that wt1b+cells migrate into the wound to form a stopper-like structure, likely to maintain structural integrity. Wt1b+sheath cells are distinct in expressing cartilage and vacuolar genes, and in repressing a Wt1b-p53 transcriptional programme. At the wound, wt1b+and entpd5+ cells constitute separate, tightly-associated subpopulations. Surprisingly, wt1b expression at the site of injury is maintained even into adult stages in developing vertebrae, which form in an untypical manner via a cartilage intermediate. Given that notochord cells are retained in adult intervertebral discs, the identification of novel subpopulations may have important implications for regenerative spine disorder treatments.
UR - http://www.scopus.com/inward/record.url?scp=85043491741&partnerID=8YFLogxK
U2 - 10.7554/eLife.30657
DO - 10.7554/eLife.30657
M3 - Article
AN - SCOPUS:85043491741
SN - 2050-084X
VL - 7
JO - eLife
JF - eLife
M1 - e30657
ER -