Regulation of erythrocyte survival by AMP-activated protein kinase

被引:180
作者
Foeller, Michael [1 ]
Sopjani, Mentor
Koka, Saisudha
Gu, Shuchen
Mahmud, Hasan
Wang, Kan
Floride, Elisa
Schleicher, Erwin [2 ]
Schulz, Eberhard [3 ]
Muenzel, Thomas [3 ]
Lang, Florian
机构
[1] Univ Tubingen, Inst Physiol, Dept Physiol, D-72076 Tubingen, Germany
[2] Univ Tubingen, Dept Endocrinol Diabet Vasc Med Nephrol & Clin Ch, D-72076 Tubingen, Germany
[3] Johannes Gutenberg Univ Mainz, Dept Cardiol, Mainz, Germany
关键词
cell volume; annexin; eryptosis; calcium; phosphatidylserine; PROGRAMMED CELL-DEATH; PHOSPHATIDYLSERINE EXPOSURE; CATION CONDUCTANCE; INHIBITION; STIMULATION; MECHANISMS; APOPTOSIS; ADHESION; CHANNELS; RECEPTOR;
D O I
10.1096/fj.08-121772
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
AMP-activated protein kinase (AMPK), an energy-sensing enzyme, counteracts energy depletion by stimulation of energy production and limitation of energy utilization. On energy depletion, erythrocytes undergo suicidal death or eryptosis, triggered by an increase in cytosolic Ca2+ activity ([Ca2+](i)) and characterized by cell shrinkage and phosphatidylserine (PS) exposure at the erythrocyte surface. The present study explored whether AMPK participates in the regulation of eryptosis. Western blotting and confocal microscopy disclosed AMPK expression in erythrocytes. [Ca2+](i) (Fluo3 fluorescence), cell volume (forward scatter), and PS exposure (annexin V binding) were determined by fluorescence-activated cell sorting (FACS) analysis. Glucose removal increased [Ca2+](i), decreased cell volume, and increased PS exposure. The AMPK-inhibitor compound C (20 mu M) did not significantly modify eryptosis under glucose-replete conditions but significantly augmented the eryptotic effect of glucose withdrawal. An increase in [Ca2+](i) by Ca2+ ionophore ionomycin triggered eryptosis, an effect blunted by the AMPK activator 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR; 1 mM). As compared with erythrocytes from wild-type littermates (ampk(+/+)), erythrocytes from AMPK alpha 1-deficient mice (ampk(-/-)) were significantly more susceptible to the eryptotic effect of energy depletion. The ampk(-/-) mice were anemic despite excessive reticulocytosis, and they suffered from severe splenomegaly, again pointing to enhanced erythrocyte turnover. The observations disclose a critical role of AMPK in the survival of circulating erythrocytes.-Foller, M., Sopjani, M., Koka, S., Gu, S., Mahmud, H., Wang, K., Floride, E., Schleicher, E., Schulz, E., Munzel, T., Lang, F. Regulation of erythrocyte survival by AMP-activated protein kinase. FASEB J. 23, 1072-1080 (2009)
引用
收藏
页码:1072 / 1080
页数:9
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