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Pgp‐positive leukaemic cells have increased mtDNA but no increased rate of proliferation
Author(s) -
Jia Li,
Liu KanZhi,
Newland Adrian C.,
Mantsch Henry H.,
Kelsey Stephen M.
Publication year - 1999
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1046/j.1365-2141.1999.01771.x
Subject(s) - cell growth , apoptosis , cancer research , mitochondrial dna , biology , medicine , immunology , genetics , gene
Cells of solid tumours tend to rely on glycolysis for energy. On the other hand, increased glycolysis in solid tumour cells expressing the multidrug resistance protein MDR‐1 has been associated with increased malignancy in tumours. We have previously shown that cells of the MDR‐1‐positive CEM/VLB 100 leukaemic cell line have increased mitochondrial electron transport chain (mtETC) activity compared with parental CEM cells. In the present study we used infrared (IR) spectroscopy to demonstrate that the mitochondrial DNA (mtDNA) content in the CEM/VLB 100 cell line was significantly increased compared to that in the parental CEM cells. The increase in mtDNA was not accompanied by an increase in mitochondrial protein as both lipid and protein levels were decreased in CEM/VLB 100 mitochondria. The ATP content was similar in these two cell lines. However, the ATP‐dependent membrane efflux pump function in CEM/VLB 100 cells was significantly reduced when mitochondrial ATP synthesis was inhibited by oligomycin, a specific inhibitor of mitochondrial F 0 F 1 ‐ATPase. Proliferation of CEM/VLB 100 cells was significantly decreased compared to parental CEM cells, and was independent of p53 expression. Thus, we conclude that: (1) IR spectroscopy is a potential powerful technique for detecting mtDNA, protein and lipid contents simultaneously; (2) leukaemic cells mainly rely on mtDNA for energy; (3) increased expression of an ATP‐dependent membrane efflux pump such as Pgp may up‐regulate ATP generation and mtDNA content. These metabolic perturbations may exist merely to serve the efflux pump and do not result in an increase in leukaemic cell proliferation. In addition, the associated reduction in mitochondrial lipid and protein may contribute to sensitize the cells to cytochrome c release.