Serum response factor function and dysfunction in smooth muscle

被引:21
作者
Camoretti-Mercado, B [1 ]
Dulin, NO [1 ]
Solway, J [1 ]
机构
[1] Univ Chicago, Dept Med, Pulm & Crit Care Med Sect, Chicago, IL 60637 USA
关键词
airway; smooth muscle; differentiation; disease; asthma; gene; expression; transcription factor; airways; vasculature; proliferation; apoptosis;
D O I
10.1016/S1569-9048(03)00149-6
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Tight control of smooth muscle cell (SM) proliferation, differentiation, and apoptosis requires a balance between signaling and transcriptional events. Recent developments in vascular research revealed that serum response factor (SRF) function is important for the regulation of each of these processes. The cloning and characterization of several SM specific genes and the discovery that SRF is central for their expression fueled studies aimed at understanding the role of molecular partners including co-activators and co-repressors. Perturbations of pathways involving SRF are associated with abnormalities in the myogenic program and aberrant phenotypic consequences. Surprisingly, studies on airway SM have remained an underrepresented area of investigation. Our laboratory described a novel regulatory mechanism of SRF function in airway myocytes by modulation of its subcellular localization. This review summarizes current knowledge on the structure and function of this essential transcription factor as well different modes of regulating SRF expression and activity that are becoming key players in directing SM function in health and disease. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:223 / 235
页数:13
相关论文
共 88 条
  • [1] AFFOLTER M, 1994, DEVELOPMENT, V120, P743
  • [2] Serum response factor is essential for mesoderm formation during mouse embryogenesis
    Arsenian, S
    Weinhold, B
    Oelgeschläger, M
    Rüther, U
    Nordheim, A
    [J]. EMBO JOURNAL, 1998, 17 (21) : 6289 - 6299
  • [3] Belaguli NS, 1999, MOL CELL BIOL, V19, P4582
  • [4] High RhoA activity maintains the undifferentiated mesenchymal cell phenotype, whereas RhoA down-regulation by laminin-2 induces smooth muscle myogenesis
    Beqaj, S
    Jakkaraju, S
    Mattingly, RR
    Pan, D
    Schuger, L
    [J]. JOURNAL OF CELL BIOLOGY, 2002, 156 (05) : 893 - 903
  • [5] Cleavage of the serum response factor during death receptor-induced apoptosis results in an inhibition of the c-FOS promoter transcriptional activity
    Bertolotto, C
    Ricci, JE
    Luciano, F
    Mari, B
    Chambard, JC
    Auberger, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) : 12941 - 12947
  • [6] Leukemia-associated Rho guanine nucleotide exchange factor promotes Gαq-coupled activation of RhoA
    Booden, MA
    Siderovski, DP
    Der, CJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (12) : 4053 - 4061
  • [7] The developmentally regulated expression of serum response factor plays a key role in the control of smooth muscle-specific genes
    Browning, CL
    Culberson, DE
    Aragon, IV
    Fillmore, RA
    Croissant, JD
    Schwartz, RJ
    Zimmer, WE
    [J]. DEVELOPMENTAL BIOLOGY, 1998, 194 (01) : 18 - 37
  • [8] Physiological control of smooth muscle-specific gene expression through regulated nuclear translocation of serum response factor
    Camoretti-Mercado, B
    Liu, HW
    Halayko, AJ
    Forsythe, SM
    Kyle, JW
    Li, B
    Fu, YP
    McConville, J
    Kogut, P
    Vieira, JE
    Patel, NM
    Hershenson, MB
    Fuchs, E
    Sinha, S
    Miano, JM
    Parmacek, MS
    Burkhardt, JK
    Solway, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) : 30387 - 30393
  • [9] RhoA GTPase and serum response factor control selectively the expression of MyoD without affecting Myf5 in mouse myoblasts
    Carnac, G
    Primig, M
    Kitzmann, M
    Chafey, P
    Tuil, D
    Lamb, N
    Fernandez, A
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (07) : 1891 - 1902
  • [10] The smooth muscle γ-actin gene promoter is a molecular target for the mouse bagpipe homologue, mNkx3-1, and serum response factor
    Carson, JA
    Fillmore, RA
    Schwartz, RJ
    Zimmer, WE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) : 39061 - 39072