4.8 Article

Mitochondrial Transfer by Photothermal Nanoblade Restores Metabolite Profile in Mammalian Cells

期刊

CELL METABOLISM
卷 23, 期 5, 页码 921-929

出版社

CELL PRESS
DOI: 10.1016/j.cmet.2016.04.007

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资金

  1. UC Discovery Biotechnology grant [178517]
  2. Air Force Office of Scientific Research grant [FA9550-15-1-0406]
  3. NIH [GM007185, GM114188, GM073981, GM061721, EB014456, CA009056, CA90571, CA009120, CA156674, CA185189, CA168585]
  4. NSF [CBET-1404080]
  5. CIRM [RB1-01397, RT3-07678]
  6. Prostate Cancer Foundation Challenge Award
  7. Broad Stem Cell Research Center Training Grant and Innovator Award
  8. American Cancer Society Research Scholar Award [RSG-12-257-01-TBE]
  9. Melanoma Research Alliance Established Investigator Award [20120279]
  10. National Center for Advancing Translational Sciences UCLA CTSI Grant [UL1TR000124]
  11. NanoCav, LLC
  12. NantWorks, LLC
  13. Div Of Chem, Bioeng, Env, & Transp Sys
  14. Directorate For Engineering [1404080] Funding Source: National Science Foundation

向作者/读者索取更多资源

mtDNA sequence alterations are challenging to generate but desirable for basic studies and potential correction of mtDNA diseases. Here, we report a new method for transferring isolated mitochondria into somatic mammalian cells using a photothermal nanoblade, which bypasses endocytosis and cell fusion. The nanoblade rescued the pyrimidine auxotroph phenotype and respiration of rho 0 cells that lack mtDNA. Three stable isogenic nanoblade-rescued clones grown in uridine-free medium showed distinct bioenergetics profiles. Rescue lines 1 and 3 reestablished nucleus-encoded anapleurotic and catapleurotic enzyme gene expression patterns and had metabolite profiles similar to the parent cells from which the rho 0 recipient cells were derived. By contrast, rescue line 2 retained a rho 0 cell metabolic phenotype despite growth in uridine-free selection. The known influence of metabolite levels on cellular processes, including epigenome modifications and gene expression, suggests metabolite profiling can help assess the quality and function of mtDNA-modified cells.

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