<i>Wilms Tumor 1b</i> defines a wound-specific sheath cell subpopulation associated with notochord repair.

Lopez-Baez, Juan Carlos; Simpson, Daniel J; LLeras Forero, Laura; Zeng, Zhiqiang; Brunsdon, Hannah; Salzano, Angela; Brombin, Alessandro; Wyatt, Cameron et al. · Elife · 2018

basic_science · Level V

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Abstract

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 <i>wt1b</i><sup>+</sup>cells migrate into the wound to form a stopper-like structure, likely to maintain structural integrity. <i>Wt1b</i><sup>+</sup>sheath cells are distinct in expressing cartilage and vacuolar genes, and in repressing a Wt1b-p53 transcriptional programme. At the wound, <i>wt1b</i><sup>+</sup>and <i>entpd5<sup>+</sup></i> cells constitute separate, tightly-associated subpopulations. Surprisingly, <i>wt1b</i> 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.

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