Lz. Xue et Jm. Lucocq, LOW EXTRACELLULAR PH INDUCES ACTIVATION OF ERK-2, JNK, AND P38 IN A431 AND SWISS 3T3 CELLS, Biochemical and biophysical research communications, 241(2), 1997, pp. 236-242
The mechanism by which mammalian cells respond to low environmental pH
is unclear. A wide range of environmental stresses are known to induc
e activation of MAP kinases ERK 2, JNK and p38 and recent work has sho
wn that low pH can activate the p38 homologue in yeast HOG1. In this s
tudy we show that ERK2 MAP kinase is activated in human A431 cells exp
osed to low pH media. Activation is sustained throughout low pH treatm
ent, is reversible, and occurs maximally at pH 4 or 5. Stimulation is
not accompanied by tyrosine phosphorylation of the EGF receptor or Raf
-1 activation, indicating that acid conditions act via pathways indepe
ndent of those required for EGF mediated MAPK stimulation. The MAP kin
ase homologue JNR and MAPKAP kinase-2 reactivating kinase (p38) were a
lso activated in A431 cells by low pH and so low pH induces parallel a
ctivation of multiple MAP kinase pathways. Strong activation of p42, a
nd p44 ERKs as well as p38 and JNK was also found in mouse Swiss 3T3 c
ells treated at pH 5. These results indicate that MAP kinases may be i
mportant markers of the acid induced cellular stress that occurs in hu
man disease. (C) 1997 Academic Press.