Bio


I am a zoologist and molecular biologist interested in the molecular basis of regeneration. My research focuses on stem cells and regeneration in ascidians, a group of marine invertebrates that represent the closest living relatives of the vertebrates. One of the main questions that motivate my research is whether regeneration capabilities lost during evolution can, at least to some extent, be re-acquired. As regeneration is not universal in the animal kingdom, I hypothesize that comparing regeneration in species with distinct regenerative capacities will lead to the discovery of key components of regeneration.
During my postdoc I intend to use comparative genomics to identify conserved cellular and molecular mechanisms that underlie ascidians’ regeneration.

Honors & Awards


  • Seal of Excellence, Marie Skłodowska-Curie Actions (2023-2025)
  • Postdoctoral fellowship, The Zuckerman STEM Leadership (2023-2024)
  • The Presidential postdoctoral scholarship, Tel Aviv University (2023-2024)
  • Covid 19 emergency postdoctoral fellowship, Israel Academy of Sciences and Humanities (2021-2022)
  • University Rector Postdoctoral Scholarships, Tel-Aviv University (2020-2021)

Professional Education


  • Doctor of Philosophy, Tel Aviv University (2021)
  • Master of Science, Tel Aviv University (2016)
  • Bachelor of Science, Tel Aviv University (2014)
  • Ph.D., Tel Aviv University, Israel, Life Science (2021)
  • M.Sc., Tel Aviv University, Israel, Ecology (2016)
  • B.Sc., Tel Aviv University, Israel, Biology (2014)

Stanford Advisors


All Publications


  • Stemness Activity Underlying Whole Brain Regeneration in a Basal Chordate. Cells Gordon, T., Zaquin, T., Kowarsky, M. A., Voskoboynik, Y., Hendin, N., Wurtzel, O., Caicci, F., Manni, L., Voskoboynik, A., Shenkar, N. 2022; 11 (23)

    Abstract

    Understanding how neurons regenerate following injury remains a central challenge in regenerative medicine. Adult mammals have a very limited ability to regenerate new neurons in the central nervous system (CNS). In contrast, the basal chordate Polycarpa mytiligera can regenerate its entire CNS within seven days of complete removal. Transcriptome sequencing, cellular labeling, and proliferation in vivo essays revealed that CNS regeneration is mediated by a newly formed neural progeny and the activation of neurodevelopmental pathways that are associated with enhanced stem-cell activity. Analyzing the expression of 239 activated pathways enabled a quantitative understanding of gene-set enrichment patterns at key regeneration stages. The molecular and cellular mechanisms controlling the regenerative ability that this study reveals can be used to develop innovative approaches to enhancing neurogenesis in closely-related chordate species, including humans.

    View details for DOI 10.3390/cells11233727

    View details for PubMedID 36496987

    View details for PubMedCentralID PMC9738451

  • Molecular characterization of the immediate wound response of the solitary ascidian Polycarpa mytiligera DEVELOPMENTAL DYNAMICS Hendin, N., Gordon, T., Shenkar, N., Wurtzel, O. 2022; 251 (12): 1968-1981

    Abstract

    Injury response is key to successful regeneration. Yet, transcriptome analyses of injury response were performed only on a handful of regenerative organisms. Here, we studied the injury response of the solitary ascidian Polycarpa mytiligera, an emerging model system, capable of regenerating any body part. We used the siphon as a model for studying transcriptional changes following injury, and identified genes that were activated in the initial 24 hours post amputation (hpa).Highly conserved genes, such as bone morphogenetic protein-1 (BMP1), growth hormone secretagogue receptor (GHSR) and IL-17, were upregulated by 12 hpa, yet their expression was sustained only in non-regenerating tissue fragments. We optimized fluorescent in situ hybridization, and found that the majority of BMP1+ cells were localized to the rigid tunic that covers the animal. This highlights the importance of this tissue, particularly during injury response. BMP1 was overexpressed following injuries to other body regions, suggesting that it was a part of a common injury-induced program.Our study suggests that, initially, specific injury-induced genes were upregulated in P. mytiligera organs, yet, later, a unique transcriptional profile was observed only in regenerating tissues. These findings highlight the importance of studying diverse regenerating and non-regenerating organisms for complete understanding of regeneration.

    View details for DOI 10.1002/dvdy.526

    View details for Web of Science ID 000857819400001

    View details for PubMedID 36001356

  • And Then There Were Three horizontal ellipsis : Extreme Regeneration Ability of the Solitary Chordate Polycarpa mytiligera FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY Gordon, T., Upadhyay, A., Manni, L., Huchon, D., Shenkar, N. 2021; 9: 652466

    Abstract

    Extensive regenerative ability is a common trait of animals capable of asexual development. The current study reveals the extraordinary regeneration abilities of the solitary ascidian Polycarpa mytiligera. Dissection of a single individual into separate fragments along two body axes resulted in the complete regeneration of each fragment into an independent, functional individual. The ability of a solitary ascidian, incapable of asexual development, to achieve bidirectional regeneration and fully regenerate all body structures and organs is described here for the first time. Amputation initiated cell proliferation in proximity to the amputation line. Phylogenetic analysis demonstrated the close affinity of P. mytiligera to colonial species. This evolutionary proximity suggests the ability for regeneration as an exaptation feature for colonial lifestyle. P. mytiligera's exceptional regenerative abilities and phylogenetic position highlight its potential to serve as a new comparative system for studies seeking to uncover the evolution of regeneration and coloniality among the chordates.

    View details for DOI 10.3389/fcell.2021.652466

    View details for Web of Science ID 000645302400001

    View details for PubMedID 33937252

    View details for PubMedCentralID PMC8083962

  • Spawning induction, development and culturing of the solitary ascidianPolycarpa mytiligera, an emerging model for regeneration studies FRONTIERS IN ZOOLOGY Gordon, T., Roth, L., Caicci, F., Manni, L., Shenkar, N. 2020; 17 (1): 19

    Abstract

    Ascidians (phylum Chordata, class Ascidiacea) represent the closest living invertebrate relatives of the vertebrates and constitute an important model for studying the evolution of chordate development. The solitary ascidian Polycarpa mytiligera exhibits a robust regeneration ability, unique among solitary chordates, thus offering a promising new model for regeneration studies. Understanding its reproductive development and establishing land-based culturing methods is pivotal for utilizing this species for experimental studies. Its reproduction cycle, spawning behavior, and developmental processes were therefore studied in both the field and the lab, and methods were developed for its culture in both open and closed water systems.Field surveys revealed that P. mytiligera's natural recruitment period starts in summer (June) and ends in winter (December) when seawater temperature decreases. Laboratory experiments revealed that low temperature (21 °C) has a negative effect on its fertilization and development. Although spontaneous spawning events occur only between June and December, we were able to induce spawning under controlled conditions year-round by means of gradual changes in the environmental conditions. Spawning events, followed by larval development and metamorphosis, took place in ascidians maintained in either artificial or natural seawater facilities. P. mytiligera's fast developmental process indicated its resemblance to other oviparous species, with the larvae initiating settlement and metamorphosis at about 12 h post-hatching, and reaching the juvenile stage 3 days later.Polycarpa mytiligera can be induced to spawn in captivity year-round, independent of the natural reproduction season. The significant advantages of P. mytiligera as a model system for regenerative studies, combined with the detailed developmental data and culturing methods presented here, will contribute to future research addressing developmental and evolutionary questions, and promote the use of this species as an applicable model system for experimental studies.

    View details for DOI 10.1186/s12983-020-00365-x

    View details for Web of Science ID 000543004700001

    View details for PubMedID 32536959

    View details for PubMedCentralID PMC7288498

  • Regeneration ability in four stolidobranch ascidians: Ecological and evolutionary implications JOURNAL OF EXPERIMENTAL MARINE BIOLOGY AND ECOLOGY Gordon, T., Manni, L., Shenkar, N. 2019; 519
  • Gut-spilling in chordates: Evisceration in the tropical ascidian Polycarpa mytiligera SCIENTIFIC REPORTS Shenkar, N., Gordon, T. 2015; 5: 9614

    Abstract

    The ejection of internal organs, i.e., evisceration, is a well-known phenomenon in sea-cucumbers. We report the ability of a member of the Chordate phyla, the tropical ascidian Polycarpa mytiligera, to eviscerate and regenerate its gut within 12 days, and to rebuild its branchial sac within 19 days. Evisceration occurred within 4-43 seconds of gentle mechanical pressure exerted on the tunic in 47% of the tested P. mytiligera. Individuals were able to discard up to 3/4 of their digestive tract via the incurrent siphon by rupture of the branchial sac in this area. Although chemical analysis revealed no significant levels of toxic compounds, the eviscerated guts were unpalatable to the triggerfish and pufferfish on which they were tested, suggesting evisceration as a defense mechanism. Given the close affinity of ascidians to vertebrates, the regeneration pathway of the viscera and branchial sac of ascidians suggests its potential beneficial application in soft tissue regeneration research.

    View details for DOI 10.1038/srep09614

    View details for Web of Science ID 000353273900001

    View details for PubMedID 25880620

    View details for PubMedCentralID PMC5381747