TY - JOUR
T1 - Adult kidney stem/progenitor cells contribute to regeneration through the secretion of trophic factors
AU - Tsuji, Kenji
AU - Kitamura, Shinji
AU - Sang, Yizhen
AU - Fukushima, Kazuhiko
AU - Wada, Jun
N1 - Funding Information:
Kenji Tsuji is supported by the Japanese Society for the Promotion of Science (JSPS)/Grant-in-Aid for Young Scientists (18K15978), Teraoka Scholarship Foundation and GSK Japan Research Grant 2018. Shinji Kitamura is supported by the Japanese Society for the Promotion of Science (JSPS)/Grant-in-Aid for Scientific research (C) (18K08244).
Funding Information:
Kenji Tsuji is supported by the Japanese Society for the Promotion of Science (JSPS)/Grant-in-Aid for Young Scientists ( 18K15978 ), Teraoka Scholarship Foundation and GSK Japan Research Grant 2018. Shinji Kitamura is supported by the Japanese Society for the Promotion of Science (JSPS)/Grant-in-Aid for Scientific research (C) (18K08244).
Publisher Copyright:
© 2020 The Authors
PY - 2020/7
Y1 - 2020/7
N2 - Adult kidney stem cells are known to have important roles in renal regeneration after acute kidney injury. Although trophic factors from tissue stem cells have been reported to promote the regeneration of other organs, there is limited number of evidence of this phenomenon in the kidneys. Here, we explored the effects of secreted factors from kidney stem cells. We intraperitoneally administered culture supernatant obtained from adult rat kidney stem/progenitor cells into rat kidney ischemia/reperfusion injury models, and the treatment significantly ameliorated renal tubulointerstitial injury, suppressed tubular cell apoptosis, diminished inflammation and promoted the proliferation of both residual renal cells and immature cells. In vitro, treatment with culture supernatant from kidney stem cells significantly promoted cell proliferation and suppressed cisplatin-induced cell apoptosis in both normal rat kidney cells and kidney stem cells. In addition, treatment with culture supernatant increased the expression of nestin in normal rat kidney cells, suggesting the dedifferentiation of tubular cells into stem-like cells. Analysis of the culture supernatant revealed that it contained a variety of growth factors. Taken together, the results suggest that these factors together lead to renal regeneration. In conclusion, adult kidney stem cells contribute to renal regeneration indirectly through the secretion of regenerative factors.
AB - Adult kidney stem cells are known to have important roles in renal regeneration after acute kidney injury. Although trophic factors from tissue stem cells have been reported to promote the regeneration of other organs, there is limited number of evidence of this phenomenon in the kidneys. Here, we explored the effects of secreted factors from kidney stem cells. We intraperitoneally administered culture supernatant obtained from adult rat kidney stem/progenitor cells into rat kidney ischemia/reperfusion injury models, and the treatment significantly ameliorated renal tubulointerstitial injury, suppressed tubular cell apoptosis, diminished inflammation and promoted the proliferation of both residual renal cells and immature cells. In vitro, treatment with culture supernatant from kidney stem cells significantly promoted cell proliferation and suppressed cisplatin-induced cell apoptosis in both normal rat kidney cells and kidney stem cells. In addition, treatment with culture supernatant increased the expression of nestin in normal rat kidney cells, suggesting the dedifferentiation of tubular cells into stem-like cells. Analysis of the culture supernatant revealed that it contained a variety of growth factors. Taken together, the results suggest that these factors together lead to renal regeneration. In conclusion, adult kidney stem cells contribute to renal regeneration indirectly through the secretion of regenerative factors.
KW - Acute kidney injury
KW - Growth factor
KW - Kidney stem cell
KW - Regeneration
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U2 - 10.1016/j.scr.2020.101865
DO - 10.1016/j.scr.2020.101865
M3 - Article
C2 - 32505897
AN - SCOPUS:85085747246
SN - 1873-5061
VL - 46
JO - Stem Cell Research
JF - Stem Cell Research
M1 - 101865
ER -