Energy depletion by cell proliferation sensitizes the kidney epithelial cells to injury

被引:1
作者
Galichon, Pierre [1 ,2 ,3 ,4 ]
Lannoy, Morgane [3 ]
Li, Li [1 ,2 ]
Serre, Justine [3 ]
Vandermeersch, Sophie [3 ]
Legouis, David [5 ]
Valerius, M. Todd [1 ,2 ]
Hadchouel, Juliette [3 ]
Bonventre, Joseph V. [1 ,2 ]
机构
[1] Harvard Med Sch, Dept Med, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Renal Div, Boston, MA 02115 USA
[3] Inst Natl Sante & Rech Medicale UMR S1155, Common & Rare & Kidney Dis, Mol Events Precis Med, Paris, France
[4] Sorbonne Univ, Med Sch, Paris, France
[5] Univ Hosp Geneva, Dept Med & Cell Physiol, Div Intens Care, Lab Nephrol, Geneva, Switzerland
关键词
acute kidney injury; cell proliferation; cell survival; energy metabolism; ischemia-reperfusion injury; INTRACELLULAR ATP; CYCLE ARREST; P53; APOPTOSIS; FIBROSIS; HYPOXIA; AMPK; MITOCHONDRIA; METABOLISM; PLATFORM;
D O I
10.1152/ajprenal.00023.2023
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Acute kidney injury activates both proliferative and antiproliferative pathways, the consequences of which are not fully elucidated. If an initial proliferation of the renal epithelium is necessary for the successful repair, the persistence of proliferation markers is associated with the occurrence of chronic kidney disease. We hypothesized that proliferation in stress conditions impacts cell viability and renal outcomes. We found that proliferation is associated with cell death after various stresses in kidney cells. In vitro, the ATP/ADP ratio oscillates reproducibly throughout the cell cycle, and cell proliferation is associated with a decreased intracellular ATP/ADP ratio. In vivo, transcriptomic data from transplanted kidneys revealed that proliferation was strongly associated with a decrease in the expression of the mitochondria-encoded genes of the oxidative phosphorylation pathway, but not of the nucleus-encoded ones. These observations suggest that mitochondrial function is a limiting factor for energy production in proliferative kidney cells after injury. The association of increased proliferation and decreased mitochondrial function was indeed associated with poor renal outcomes. In summary, proliferation is an energy-demanding process impairing the cellular ability to cope with an injury, highlighting proliferative repair and metabolic recovery as indispensable and interdependent features for successful kidney repair. NEW & NOTEWORTHY ATP depletion is a hallmark of acute kidney injury. Proliferation is instrumental to kidney repair. We show that ATP levels vary during the cell cycle and that proliferation sensitizes renal epithelial cells to superimposed injuries in vitro. More proliferation and less energy production by the mitochondria are associated with adverse outcomes in injured kidney allografts. This suggests that controlling the timing of kidney repair might be beneficial to mitigate the extent of acute kidney injury.
引用
收藏
页码:F326 / F337
页数:12
相关论文
共 50 条
  • [41] TRIP13-deficient tubular epithelial cells are susceptible to apoptosis following acute kidney injury
    Pressly, Jeffrey D.
    Hama, Taketsugu
    O' Brien, Shannon
    Regner, Kevin R.
    Park, Frank
    SCIENTIFIC REPORTS, 2017, 7
  • [42] Alteration of fatty acid oxidation in tubular epithelial cells: from acute kidney injury to renal fibrogenesis
    Simon, Noemie
    Hertig, Alexandre
    FRONTIERS IN MEDICINE, 2015, 2
  • [43] Effect and mechanism of erythropoietin on mesenchymal stem cell proliferation in vitro under the acute kidney injury microenvironment
    Liu, Nanmei
    Tian, Jun
    Wang, Weiwei
    Cheng, Jin
    Hu, Dayong
    Zhang, Jinyuan
    EXPERIMENTAL BIOLOGY AND MEDICINE, 2011, 236 (09) : 1093 - 1099
  • [44] miR-204 regulates epithelial-mesenchymal transition by targeting SP1 in the tubular epithelial cells after acute kidney injury induced by ischemia-reperfusion
    Chen, Shun-Jie
    Wu, Ping
    Sun, Li-Jing
    Zhou, Bo
    Niu, Wei
    Liu, Shuang
    Lin, Fu-Jun
    Jiang, Geng-Ru
    ONCOLOGY REPORTS, 2017, 37 (02) : 1148 - 1158
  • [45] Polyamine depletion stabilizes p53 resulting in inhibition of normal intestinal epithelial cell proliferation
    Li, L
    Rao, JN
    Guo, X
    Liu, L
    Santora, R
    Bass, BL
    Wang, JY
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 281 (03): : C941 - C953
  • [46] Preparation of epithelial cell aggregates incorporating matrigel microspheres to enhance proliferation and differentiation of epithelial cells
    Tajima, Shuhei
    Tabata, Yasuhiko
    REGENERATIVE THERAPY, 2017, 7 : 34 - 44
  • [47] The cell cycle and acute kidney injury
    Price, Peter M.
    Safirstein, Robert L.
    Megyesi, Judit
    KIDNEY INTERNATIONAL, 2009, 76 (06) : 604 - 613
  • [48] Kidney epithelial targeted mitochondrial transcription factor A deficiency results in progressive mitochondrial depletion associated with severe cystic disease
    Ishii, Ken
    Kobayashi, Hanako
    Taguchi, Kensei
    Guan, Nan
    Li, Andraia
    Tong, Carmen
    Davidoff, Olena
    Tran, Pamela, V
    Sharma, Madhulika
    Chandel, Navdeep S.
    Kapp, Meghan E.
    Fogo, Agnes B.
    Brooks, Craig R.
    Haase, Volker H.
    KIDNEY INTERNATIONAL, 2021, 99 (03) : 657 - 670
  • [49] Interaction Between Intrinsic Renal Cells and Immune Cells in the Progression of Acute Kidney Injury
    Deng, Junhui
    Wu, Zhifen
    He, Yun
    Lin, Lirong
    Tan, Wei
    Yang, Jurong
    FRONTIERS IN MEDICINE, 2022, 9
  • [50] Effect of sodium butyrate on cell proliferation and cell cycle in porcine intestinal epithelial (IPEC-J2) cells
    Yueqin Qiu
    Xianyong Ma
    Xuefen Yang
    Li Wang
    Zongyong Jiang
    In Vitro Cellular & Developmental Biology - Animal, 2017, 53 : 304 - 311