Growth and cell density-dependent expression of stathmin in C2 myoblasts in culture

被引:35
作者
Balogh, A [1 ]
Mege, RM [1 ]
Sobel, A [1 ]
机构
[1] INSERM, U153, F-75005 PARIS, FRANCE
关键词
D O I
10.1006/excr.1996.0106
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Stathmin is a 19-kDa, ubiquitous cytoplasmic phosphoprotein whose expression is strongly regulated during tissue development and maturation and which was proposed as a general relay integrating diverse intracellular signaling pathways. Since myoblasts tend to align and differentiate in vitro toward myotubes above a certain density in culture, we examined the expression of stathmin as a function of cell density in the C2 myogenic cell line. Whereas stathmin was hardly detectable in low- to medium-density cultures corresponding to less than 1 mu g soluble protein/cm(2), it became expressed to a stable level above this threshold of cell density. This cell density effect on stathmin expression was not mediated by a diffusible factor, since myogenic C2 or fibroblastic 3T3 cells grown at low and high density within the same culture dash displayed the same pattern of density-dependent stathmin expression, significant stathmin levels being observed only in the dense moiety of the flask. Interestingly, culture conditions which indirectly perturb cell-cell contacts, such as low Ca2+ or incubation with cytoskeleton disrupting agents such as nocodazole or cytochalasin D, prevented the expression of stathmin in C2 cells even at high density. More directly, anti-E-cadherin immunoglobulins, interfering with direct cell-cell contacts of the E-cadherin expressing S180 sarcoma-derived 2B2 cells, also prevented the expression of stathmin in these cells even at high density. Altogether, our results indicate that cell-cell contacts, probably mediated by adhesion molecules such as cadherins, are responsible for the high-density-induced expression of stathmin, which might then participate, in particular in the case of myogenic cells, in the control of the proliferation of cells and of their entry into the differentiation process. (C) 1996 Academic Press, Inc
引用
收藏
页码:8 / 15
页数:8
相关论文
共 65 条
  • [1] NEURAL CELL-ADHESION MOLECULE MEDIATES CONTACT-DEPENDENT INHIBITION OF GROWTH OF NEAR-DIPLOID MOUSE FIBROBLAST CELL-LINE M5S/1M
    AOKI, J
    UMEDA, M
    TAKIO, K
    TITANI, K
    UTSUMI, H
    SASAKI, M
    INOUE, K
    [J]. JOURNAL OF CELL BIOLOGY, 1991, 115 (06) : 1751 - 1761
  • [2] CULTURE AT HIGH-DENSITY INCREASES PHOSPHOENOLPYRUVATE CARBOXYKINASE MESSENGER-RNA IN H4IIEC3 HEPATOMA-CELLS
    BEALE, EG
    SCHAEFER, IM
    LI, Q
    [J]. MOLECULAR ENDOCRINOLOGY, 1991, 5 (05) : 661 - 669
  • [3] STATHMIN IS A MAJOR SUBSTRATE FOR MITOGEN-ACTIVATED PROTEIN-KINASE DURING HEAT-SHOCK AND CHEMICAL STRESS IN HELA-CELLS
    BERETTA, L
    DUBOIS, MF
    SOBEL, A
    BENSAUDE, O
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 227 (1-2): : 388 - 395
  • [4] BERETTA L, 1993, J BIOL CHEM, V268, P20076
  • [5] PHOSPHORYLATION OF A GROUP OF PROTEINS RELATED TO THE PHYSIOLOGICAL, MULTIHORMONAL REGULATIONS OF THE VARIOUS CELL-TYPES IN THE ANTERIOR-PITUITARY GLAND
    BERETTA, L
    BOUTTERIN, MC
    DROUVA, SV
    SOBEL, A
    [J]. ENDOCRINOLOGY, 1989, 125 (03) : 1358 - 1364
  • [6] PHOSPHORYLATION OF INTRACELLULAR PROTEINS RELATED TO THE MULTIHORMONAL REGULATION OF PROLACTIN - COMPARISON OF NORMAL ANTERIOR-PITUITARY CELLS IN CULTURE WITH THE TUMOR-DERIVED GH CELL-LINES
    BERETTA, L
    BOUTTERIN, MC
    SOBEL, A
    [J]. ENDOCRINOLOGY, 1988, 122 (01) : 40 - 51
  • [7] CELL-CYCLE-REGULATED PHOSPHORYLATION OF ONCOPROTEIN-18 ON SER16, SER25 AND SER38
    BRATTSAND, G
    MARKLUND, U
    NYLANDER, K
    ROOS, G
    GULLBERG, M
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 220 (02): : 359 - 368
  • [8] BRAVERMAN R, 1986, J BIOL CHEM, V261, P14342
  • [9] STATHMIN PHOSPHORYLATION IS REGULATED IN STRIATAL NEURONS BY VASOACTIVE-INTESTINAL-PEPTIDE AND MONOAMINES VIA MULTIPLE INTRACELLULAR PATHWAYS
    CHNEIWEISS, H
    CORDIER, J
    SOBEL, A
    [J]. JOURNAL OF NEUROCHEMISTRY, 1992, 58 (01) : 282 - 289
  • [10] STATHMIN IS A MAJOR PHOSPHOPROTEIN AND CYCLIC AMP-DEPENDENT PROTEIN-KINASE SUBSTRATE IN MOUSE-BRAIN NEURONS BUT NOT IN ASTROCYTES IN CULTURE - REGULATION DURING ONTOGENESIS
    CHNEIWEISS, H
    BERETTA, L
    CORDIER, J
    BOUTTERIN, MC
    GLOWINSKI, J
    SOBEL, A
    [J]. JOURNAL OF NEUROCHEMISTRY, 1989, 53 (03) : 856 - 863