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Impact of Cyclin-Dependent Kinase CDK4 Inhibition on Eryptosis
Author(s) -
Elisabeth Lang,
Christine Zelenak,
Matthias Eberhard,
Rosi Bissinger,
Anand Rotte,
Mehrdad Ghashghaeinia,
Adrian Lupescu,
Florian Läng,
Syed M. Qadri
Publication year - 2015
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000430241
Subject(s) - phosphatidylserine , apoptosis , programmed cell death , protein kinase c , microbiology and biotechnology , biology , annexin , cytosol , kinase , annexin a5 , protein kinase a , cyclin dependent kinase 4 , chemistry , cyclin dependent kinase 2 , biochemistry , phospholipid , membrane , enzyme
The cyclin-dependent kinase 4 (CDK4) participates in the regulation of apoptosis of nucleated cells by altering transcriptional regulation of genes governing cell proliferation and cell death. Similar to apoptosis of nucleated cells, erythrocytes may enter eryptosis, which is characterized by cell shrinkage and cell membrane scrambling with phosphatidylserine (PS) exposure at the cell surface. As mature erythrocytes lack nuclei, acute stimulation of eryptosis cannot result from altered gene expression. Eryptosis is triggered by isotonic cell shrinkage following Cl- removal (replacement with the impermeant organic anion gluconate) or by oxidative stress (exposure to 0.3 mM tertbutyl-hydroperoxide [tBOOH]). The present study explored whether CDK4 is expressed in erythrocytes and whether the CDK4 inhibitors II (NSC625987) and III (ryuvidine) influence eryptosis.

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