TY - JOUR
T1 - Preconditioning allows engraftment of mouse and human embryonic lung cells, enabling lung repair in mice
AU - Rosen, Chava
AU - Shezen, Elias
AU - Aronovich, Anna
AU - Klionsky, Yael Zlotnikov
AU - Yaakov, Yasmin
AU - Assayag, Miri
AU - Biton, Inbal Eti
AU - Tal, Orna
AU - Shakhar, Guy
AU - Ben-Hur, Herzel
AU - Shneider, David
AU - Vaknin, Zvi
AU - Sadan, Oscar
AU - Evron, Shmuel
AU - Freud, Enrique
AU - Shoseyov, David
AU - Wilschanski, Michael
AU - Berkman, Neville
AU - Fibbe, Willem E.
AU - Hagin, David
AU - Hillel-Karniel, Carmit
AU - Krentsis, Irit Milman
AU - Bachar-Lustig, Esther
AU - Reisner, Yair
N1 - Publisher Copyright:
© 2015 Nature America, Inc. All rights reserved.
PY - 2015/8/8
Y1 - 2015/8/8
N2 - Repair of injured lungs represents a longstanding therapeutic challenge. We show that human and mouse embryonic lung tissue from the canalicular stage of development (20-22 weeks of gestation for humans, and embryonic day 15-16 (E15-E16) for mouse) are enriched with progenitors residing in distinct niches. On the basis of the marked analogy to progenitor niches in bone marrow (BM), we attempted strategies similar to BM transplantation, employing sublethal radiation to vacate lung progenitor niches and to reduce stem cell competition. Intravenous infusion of a single cell suspension of canalicular lung tissue from GFP-marked mice or human fetal donors into naphthalene-injured and irradiated syngeneic or SCID mice, respectively, induced marked long-term lung chimerism. Donor type structures or 'patches' contained epithelial, mesenchymal and endothelial cells. Transplantation of differentially labeled E16 mouse lung cells indicated that these patches were probably of clonal origin from the donor. Recipients of the single cell suspension transplant exhibited marked improvement in lung compliance and tissue damping reflecting the energy dissipation in the lung tissues. Our study provides proof of concept for lung reconstitution by canalicular-stage human lung cells after preconditioning of the pulmonary niche.
AB - Repair of injured lungs represents a longstanding therapeutic challenge. We show that human and mouse embryonic lung tissue from the canalicular stage of development (20-22 weeks of gestation for humans, and embryonic day 15-16 (E15-E16) for mouse) are enriched with progenitors residing in distinct niches. On the basis of the marked analogy to progenitor niches in bone marrow (BM), we attempted strategies similar to BM transplantation, employing sublethal radiation to vacate lung progenitor niches and to reduce stem cell competition. Intravenous infusion of a single cell suspension of canalicular lung tissue from GFP-marked mice or human fetal donors into naphthalene-injured and irradiated syngeneic or SCID mice, respectively, induced marked long-term lung chimerism. Donor type structures or 'patches' contained epithelial, mesenchymal and endothelial cells. Transplantation of differentially labeled E16 mouse lung cells indicated that these patches were probably of clonal origin from the donor. Recipients of the single cell suspension transplant exhibited marked improvement in lung compliance and tissue damping reflecting the energy dissipation in the lung tissues. Our study provides proof of concept for lung reconstitution by canalicular-stage human lung cells after preconditioning of the pulmonary niche.
UR - http://www.scopus.com/inward/record.url?scp=84938803124&partnerID=8YFLogxK
U2 - 10.1038/nm.3889
DO - 10.1038/nm.3889
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C2 - 26168294
AN - SCOPUS:84938803124
SN - 1078-8956
VL - 21
SP - 869
EP - 879
JO - Nature Medicine
JF - Nature Medicine
IS - 8
ER -