Hypertonicity activates GSK3β in tumor cells

被引:8
作者
Perez-Pinera, Pablo
Menendez-Gonzalez, Manuel
del Valle, Miguel
Vega, Jose Antonio
机构
[1] Univ Oviedo, Dept Morfol & Biol Celular, Fac Med, E-33006 Oviedo, Spain
[2] Hosp Univ Cent Asturias, Oviedo, Spain
[3] Univ Oviedo, Inst Univ Oncol, E-33006 Oviedo, Spain
[4] Univ Sao Pablo CEU, Fac Med, Secc Anat & Embriol, Dept Ciencias Med, Madrid, Spain
关键词
GSK3; beta; hypertonicity; NaCl; cell signaling;
D O I
10.1007/s11010-006-9201-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Responses to perturbations in the composition of the extracellular environment are crucial to maintain cell and tissue homeostasis. In hypertonic conditions cell lines derived from kidney epithelium initiate a variety of stress responses to maintain cell viability that include activation of Mitogen Activated Protein Kinases (MAPK). We previously showed that NaCl also regulates MAPK in different tumor cell lines and we now show that when hypertonic conditions induced with NaCl and other osmolytes were used to stimulate several tumor cell lines, Glycogen Synthase Kinase 3 beta (GSK3 beta) was rapidly dephosphorylated at serine 9 and its kinase activity was increased. This response was both time- and dose-dependent, it was independent of the Akt signaling pathway and did not increase steady state levels of phosphorylation of beta-catenin, although the data suggested that activated GSK3 beta could regulate the activity of ERK1/2.
引用
收藏
页码:93 / 100
页数:8
相关论文
共 12 条
[1]
Renal papillary necrosis - 40 years on [J].
Bach, PH ;
Thanh, NTK .
TOXICOLOGIC PATHOLOGY, 1998, 26 (01) :73-91
[2]
BURG MB, 1995, AM J PHYSIOL, V268, P983
[3]
Regulatory volume increase is associated with p38 kinase-dependent actin cytoskeleton remodeling in rat kidney MTAL [J].
Bustamante, M ;
Roger, F ;
Bochaton-Piallat, ML ;
Gabbiani, G ;
Martin, PY ;
Féraille, E .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2003, 285 (02) :F336-F347
[4]
The multifaceted roles of glycogen synthase kinase 3β in cellular signaling [J].
Grimes, CA ;
Jope, RS .
PROGRESS IN NEUROBIOLOGY, 2001, 65 (04) :391-426
[5]
The glamour and gloom of glycogen synthase kinase-3 [J].
Jope, RS ;
Johnson, GVW .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (02) :95-102
[6]
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer [J].
Li, J ;
Yen, C ;
Liaw, D ;
Podsypanina, K ;
Bose, S ;
Wang, SI ;
Puc, J ;
Miliaresis, C ;
Rodgers, L ;
McCombie, R ;
Bigner, SH ;
Giovanella, BC ;
Ittmann, M ;
Tycko, B ;
Hibshoosh, H ;
Wigler, MH ;
Parsons, R .
SCIENCE, 1997, 275 (5308) :1943-1947
[7]
Maier D, 1999, CANCER RES, V59, P5479
[8]
IN DEFENSE OF CELL-VOLUME [J].
PARKER, JC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (05) :C1191-C1200
[9]
PEREZPINERA P, IN PRESS MOL CELL BI
[10]
Hypertonic stress activates glycogen synthase kinase 3β-mediated apoptosis of renal medullary interstitial cells, suppressing an NFκB-driven cyclooxygenase-2-dependent survival pathway [J].
Rao, R ;
Hao, CM ;
Breyer, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (06) :3949-3955