TY - JOUR
T1 - Salisphere derived c-Kit+ cell transplantation restores tissue homeostasis in irradiated salivary gland
AU - Nanduri, Lalitha S.Y.
AU - Lombaert, Isabelle M.A.
AU - Van Der Zwaag, Marianne
AU - Faber, Hette
AU - Brunsting, Jeanette F.
AU - Van Os, Ronald P.
AU - Coppes, Robert P.
N1 - Funding Information:
This work was supported financially by grants from the Dutch Society for Cancer Research (RUG2003-2909 and RUG 2008-4022).
PY - 2013/9
Y1 - 2013/9
N2 - Introduction During radiotherapy salivary glands of head and neck cancer patients are unavoidably co-irradiated, potentially resulting in life-long impairment. Recently we showed that transplantation of salisphere-derived c-Kit expressing cells can functionally regenerate irradiated salivary glands. This study aims to select a more potent subpopulation of c-Kit+ cells, co-expressing stem cell markers and to investigate whether long-term tissue homeostasis is restored after stem cell transplantation. Methods and results Salisphere derived c-Kit+ cells that co-expressed CD24 and/or CD49f markers, were intra-glandularly injected into 15 Gy irradiated submandibular glands of mice. Particularly, c-Kit+/CD24+/CD49f + cell transplanted mice improved saliva production (54.59 ± 11.1%) versus the irradiated control group (21.5 ± 8.7%). Increase in expression of cells with differentiated duct cell markers like, cytokeratins (CK8, 18, 7 and 14) indicated functional recovery of this compartment. Moreover, ductal stem cell marker expression like c-Kit, CD133, CD24 and CD49f reappeared after transplantation indicating long-term functional maintenance potential of the gland. Furthermore, a normalization of vascularization as indicated by CD31 expression and reduction of fibrosis was observed, indicative of normalization of the microenvironment. Conclusions Our results show that stem cell transplantation not only rescues hypo-salivation, but also restores tissue homeostasis of the irradiated gland, necessary for long-term maintenance of adult tissue.
AB - Introduction During radiotherapy salivary glands of head and neck cancer patients are unavoidably co-irradiated, potentially resulting in life-long impairment. Recently we showed that transplantation of salisphere-derived c-Kit expressing cells can functionally regenerate irradiated salivary glands. This study aims to select a more potent subpopulation of c-Kit+ cells, co-expressing stem cell markers and to investigate whether long-term tissue homeostasis is restored after stem cell transplantation. Methods and results Salisphere derived c-Kit+ cells that co-expressed CD24 and/or CD49f markers, were intra-glandularly injected into 15 Gy irradiated submandibular glands of mice. Particularly, c-Kit+/CD24+/CD49f + cell transplanted mice improved saliva production (54.59 ± 11.1%) versus the irradiated control group (21.5 ± 8.7%). Increase in expression of cells with differentiated duct cell markers like, cytokeratins (CK8, 18, 7 and 14) indicated functional recovery of this compartment. Moreover, ductal stem cell marker expression like c-Kit, CD133, CD24 and CD49f reappeared after transplantation indicating long-term functional maintenance potential of the gland. Furthermore, a normalization of vascularization as indicated by CD31 expression and reduction of fibrosis was observed, indicative of normalization of the microenvironment. Conclusions Our results show that stem cell transplantation not only rescues hypo-salivation, but also restores tissue homeostasis of the irradiated gland, necessary for long-term maintenance of adult tissue.
KW - Regeneration
KW - Salivary gland
KW - Stem cell
KW - Tissue homeostasis
KW - c-Kit
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U2 - 10.1016/j.radonc.2013.05.020
DO - 10.1016/j.radonc.2013.05.020
M3 - Article
C2 - 23769181
AN - SCOPUS:84887019857
SN - 0167-8140
VL - 108
SP - 458
EP - 463
JO - Radiotherapy and Oncology
JF - Radiotherapy and Oncology
IS - 3
ER -