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5018274 
Journal Article 
Lung injury repair by transplantation of adult lung cells following preconditioning of recipient mice 
Milman Krentsis, I; Rosen, C; Shezen, E; Aronovich, A; Nathanson, B; Bachar-Lustig, E; Berkman, N; Assayag, M; Shakhar, G; Feferman, T; Orgad, R; Reisner, Y 
2018 
68-77 
English 
Repair of injured lungs represents a longstanding therapeutic challenge. We recently demonstrated that human and mouse embryonic lung tissue from the canalicular stage of development are enriched with lung progenitors, and that a single cell suspension of canalicular lungs can be used for transplantation, provided that lung progenitor niches in the recipient mice are vacated by strategies similar to those used in bone marrow transplantation. Considering the ethical limitations associated with the use of fetal cells, we investigated here whether adult lungs could offer an alternative source of lung progenitors for transplantation. We show that intravenous infusion of a single cell suspension of adult mouse lungs from GFP+ donors, following conditioning of recipient mice with naphthalene and subsequent sublethal irradiation, led to marked colonization of the recipient lungs, at 6-8 weeks post-transplant, with donor derived structures including epithelial, endothelial, and mesenchymal cells. Epithelial cells within these donor-derived colonies expressed markers of functionally distinct lung cell types, and lung function, which is significantly compromised in mice treated with naphthalene and radiation, was found to be corrected following transplantation. Dose response analysis suggests that the frequency of patch forming cells in adult lungs was about threefold lower compared to that found in E16 fetal lungs. However, as adult lungs are much larger, the total number of patch forming cells that can be collected from this source is significantly greater. Our study provides proof of concept for lung regeneration by adult lung cells after preconditioning to vacate the pulmonary niche. Stem Cells Translational Medicine 2018;7:68-77. 
Naphthalenes; naphthalene; 2166IN72UN; Index Medicus; Transplantation; Progenitors; Animals; Mice, Inbred C57BL; Naphthalenes -- toxicity; Cells, Cultured; Mice, Knockout; Stem Cell Transplantation; Stem Cells -- cytology; Guided Tissue Regeneration -- methods; Epithelial Cells -- cytology; Lung -- cytology; Lung -- pathology; Lung Injury -- therapy; Epithelial Cells -- transplantation 
IRIS
• Naphthalene
     Database Searches
          PubMed
          WOS
     Combined data set
          Data set for title/abstract screening
               Excluded - PECO criteria not met (TIAB)
     Supplemental material
          Non-PECO routes of exposure
          Mechanistic
               Mechanisms of cancer
     Feb 2019 Update
          PubMed
          WOS
Other
• Naphthalene (2021 Evidence mapping publication)
     Database Searches
          PubMed
          WOS
     Combined data set
          Data set for title/abstract screening
               Excluded – PECO criteria not met
     Supplemental material
          Exposure routes other than inhalation, oral, or dermal (animal studies)
          Mechanistic
               Mechanisms of cancer
     Feb 2019 Update
          PubMed
          WOS