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Ouabain-regulated phosphoproteome reveals molecular mechanisms for Na+, K+-ATPase control of cell adhesion, proliferation, and survival

Panizza, Elena (författare)
Karolinska Inst, Sci Life Lab, Dept Oncol Pathol, Solna, Sweden.;Cornell Univ, Ithaca, NY USA.
Zhang, Liang (författare)
Karolinska Institutet
Fontana, Jacopo M. (författare)
KTH,Science for Life Laboratory, SciLifeLab,Tillämpad fysik
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Hamada, Kozo (författare)
RIKEN, Brain Sci Inst, Lab Dev Neurobiol, Saitama, Japan.
Svensson, Daniel (författare)
Karolinska Inst, Dept Womens & Childrens Hlth, Solna, Sweden.
Akkuratov, Evgeny E. (författare)
KTH,Biofysik,Science for Life Laboratory, SciLifeLab
Scott, Lena (författare)
Karolinska Inst, Dept Womens & Childrens Hlth, Solna, Sweden.
Mikoshiba, Katsuhiko (författare)
RIKEN, Brain Sci Inst, Lab Dev Neurobiol, Saitama, Japan.
Brismar, Hjalmar (författare)
Karolinska Institutet,KTH,Science for Life Laboratory, SciLifeLab,Tillämpad fysik,Karolinska Inst, Dept Womens & Childrens Hlth, Solna, Sweden.
Lehtio, Janne (författare)
Karolinska Institutet
Aperia, Anita (författare)
Karolinska Institutet
visa färre...
Karolinska Institutet Karolinska Inst, Sci Life Lab, Dept Oncol Pathol, Solna, Sweden;Cornell Univ, Ithaca, NY USA. (creator_code:org_t)
FEDERATION AMER SOC EXP BIOL, 2019
2019
Engelska.
Ingår i: The FASEB Journal. - : FEDERATION AMER SOC EXP BIOL. - 0892-6638 .- 1530-6860. ; 33:9, s. 10193-10206
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The ion pump Na+, K+-ATPase (NKA) is a receptor for the cardiotonic steroid ouabain. Subsaturating concentration of ouabain triggers intracellular calcium oscillations, stimulates cell proliferation and adhesion, and protects from apoptosis. However, it is controversial whether ouabain-bound NKA is considered a signal transducer. To address this question, we performed a global analysis of protein phosphorylation in COS-7 cells, identifying 2580 regulated phosphorylation events on 1242 proteins upon 10- and 20-min treatment with ouabain. Regulated phosphorylated proteins include the inositol triphosphate receptor and stromal interaction molecule, which are essential for initiating calcium oscillations. Hierarchical clustering revealed that ouabain triggers a structured phosphorylation response that occurs in a well-defined, time-dependent manner and affects specific cellular processes, including cell proliferation and cell-cell junctions. We additionally identify regulation of the phosphorylation of several calcium and calmodulin-dependent protein kinases (CAMKs), including 2 sites of CAMK type II-gamma (CAMK2G), a protein known to regulate apoptosis. To verify the significance of this result, CAMK2G was knocked down in primary kidney cells. CAMK2G knockdown impaired ouabain-dependent protection from apoptosis upon treatment with high glucose or serum deprivation. In conclusion, we establish NKA as the coordinator of a broad, tightly regulated phosphorylation response in cells and define CAMK2G as a downstream effector of NKA.-Panizza, E., Zhang, L., Fontana, J. M., Hamada, K., Svensson, D., Akkuratov, E. E., Scott, L., Mikoshiba, K., Brismar, H., Lehtio, J., Aperia, A. Ouabain-regulated phosphoproteome reveals molecular mechanisms for Na+, K+-ATPase control of cell adhesion, proliferation, and survival.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

calcium and calmodulin-dependent protein kinase
phosphoproteomics
apoptosis
inositol triphosphate receptor
kidney

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