PH nanoenvironment at the surface of single melanoma cells

被引:100
作者
Stock, Christian
Mueller, Markus
Kraehling, Hermann
Mally, Sabine
Noeel, Josette
Eder, Claudia
Schwab, Albrecht
机构
[1] Univ Munster, Inst Physiol 2, D-48149 Munster, Germany
[2] Univ Munster, Inst Physiol 2, D-4400 Munster, Germany
[3] Univ Montreal, Dept Physiol, Montreal, PQ H3C 3J7, Canada
[4] Fac Med Charite, Inst Physiol, Berlin, Germany
关键词
adhesion; cell/matrix interaction; H+ gradient; migration; NHE1; NA-H EXCHANGER; RENAL EPITHELIAL-CELLS; INTRACELLULAR PH; EXTRACELLULAR PH; NA+/H+ EXCHANGE; NUDE-MICE; MIGRATION; INTEGRIN; NHE1; ACTIVATION;
D O I
10.1159/000107550
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Extracellular pH and the Na+/ H+ exchanger ( NHE1) modulate tumor cell migration. Yet, the pH nanoenvironment at the outer surface of the cell membrane ( pH (em)) where cell/ matrix interaction occurs and matrix metalloproteinases work was never measured. We present a method to measure this pH nanoenvironment using proton-sensitive dyes to label the outer leaflet of the plasma membrane or the glycocalyx of human melanoma cells. Polarized cells generate an extracellular proton gradient at their surface that increases from the rear end to the leading edge of the lamellipodium along the direction of movement. This gradient collapses upon NHE1 inhibition by HOE642. NHE1 stimulation by intracellular acidification increases the difference in pH em between the tips of lamellipodia and the cell body in a Na+ dependent way. Thus, cells create a pH nano- environment that promotes cell migration by facilitating cell adhesion at their front and the release of cell/ matrix contacts at their rear part.
引用
收藏
页码:679 / 686
页数:8
相关论文
共 34 条
[1]  
BAILEY J, 1988, J CELL SCI, V90, P215
[2]   Nascent focal adhesions are responsible for the generation of strong propulsive forces in migrating fibroblasts [J].
Beningo, KA ;
Dembo, M ;
Kaverina, I ;
Small, JV ;
Wang, YL .
JOURNAL OF CELL BIOLOGY, 2001, 153 (04) :881-887
[3]   Glycosaminoglycans modulate C6 glioma cell adhesion to extracellular matrix components and alter cell proliferation and cell migration [J].
de Aguiar, CBNM ;
Lobao-Soares, B ;
Alvarez-Silva, M ;
Trentin, AG .
BMC CELL BIOLOGY, 2005, 6 (1)
[4]   Cell migration requires both ion translocation and cytoskeletal anchoring by the Na-H exchanger NHE1 [J].
Denker, SP ;
Barber, DL .
JOURNAL OF CELL BIOLOGY, 2002, 159 (06) :1087-1096
[5]   Direct binding of the Na-H exchanger NHE1 to ERM proteins regulates the cortical cytoskeleton and cell shape independently of H+ translocation [J].
Denker, SP ;
Huang, DC ;
Orlowski, J ;
Furthmayr, H ;
Barber, DL .
MOLECULAR CELL, 2000, 6 (06) :1425-1436
[6]   The α2β1 integrin inhibitor rhodocetin binds to the A-domain of the integrin α2 subunit proximal to the collagen-binding site [J].
Eble, JA ;
Tuckwell, DS .
BIOCHEMICAL JOURNAL, 2003, 376 :77-85
[7]   New functions for the matrix metalloproteinases in cancer progression [J].
Egeblad, M ;
Werb, Z .
NATURE REVIEWS CANCER, 2002, 2 (03) :161-174
[8]   Comparison of reagents for shape analysis of fixed cells by automated fluorescence microscopy [J].
Elliott, JT ;
Tona, A ;
Plant, AL .
CYTOMETRY PART A, 2003, 52A (02) :90-100
[9]   High-resolution CryoFESEM of individual cell adhesion molecules (CAMs) in the glycocalyx of human platelets:: Detection of P-selectin (CD62P), GPI-IX complex (CD42a/CD42bα,bβ), and integrin GPIIbIIIa (CD41/CD61) by immunogold labeling and stereo imaging [J].
Erlandsen, SL ;
Bittermann, AG ;
White, J ;
Leith, A ;
Marko, M .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2001, 49 (07) :809-819
[10]   pH- and temperature-dependence of functional modulation in metalloproteinases. A comparison between neutrophil collagenase and gelatinases A and B [J].
Fasciglione, GF ;
Marini, S ;
D'Alessio, S ;
Politi, V ;
Coletta, M .
BIOPHYSICAL JOURNAL, 2000, 79 (04) :2138-2149