Mechanisms controlling the expression of the components of the exocytotic apparatus under physiological and pathological conditions

被引:18
作者
Abderrahmani, A.
Plaisance, V.
Lovis, P.
Regazzi, R.
机构
[1] Univ Lausanne, Dept Cell Biol & Morphol, CH-1005 Lausanne, Switzerland
[2] Univ Lausanne, Dept Internal Med, CH-1005 Lausanne, Switzerland
关键词
diabetes mellitus; exocytotic apparatus; inducible cAMP early repressor (ICER); microRNA (miRNA); Rab; transcription factor;
D O I
10.1042/BST0340696
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The last decade has witnessed spectacular progress in the identification of the protein apparatus required for exocytosis of neurotransmitters, peptide hormones and other bioactive products. in striking contrast, our knowledge of the mechanisms determining the expression of the components of the secretory machinery has remained rudimentary. Since modifications in secretory functions are associated with several physiological processes and contribute to the development of human pathologies, a better knowledge of the control of the expression of the genes involved in exocytosis is urgently needed. Recent studies have led to the identification of transcription factors and other regulatory molecules such as microRNAs that modulate the cellular level of key controllers of the exocytotic process. These findings furnish a new perspective for understanding how secretory functions can adapt to normal physiological conditions and shed light on the mechanisms involved in the development of important human diseases such as diabetes mellitus characterized by defective release of bioactive compounds.
引用
收藏
页码:696 / 700
页数:5
相关论文
共 34 条
[1]   ICER induced by hyperglycemia represses the expression of genes essential for insulin exocytosis [J].
Abderrahmani, A ;
Cheviet, S ;
Ferdaoussi, M ;
Coppola, T ;
Waeber, G ;
Regazzi, R .
EMBO JOURNAL, 2006, 25 (05) :977-986
[2]   Complexin I regulates glucose-induced secretion in pancreatic β-cells [J].
Abderrahmani, A ;
Niederhauser, G ;
Plaisance, V ;
Roehrich, ME ;
Lenain, V ;
Coppola, T ;
Regazzi, R ;
Waeber, G .
JOURNAL OF CELL SCIENCE, 2004, 117 (11) :2239-2247
[3]   Neuronal traits are required for glucose-induced insulin secretion [J].
Abderrahmani, A ;
Niederhauser, G ;
Plaisance, V ;
Haefliger, JA ;
Regazzi, R ;
Waeber, G .
FEBS LETTERS, 2004, 565 (1-3) :133-138
[4]   The transcriptional repressor REST determines the cell-specific expression of the human MAPK8IP1 gene encoding IB1 (JIP-1) [J].
Abderrahmani, A ;
Steinmann, M ;
Plaisance, V ;
Niederhauser, G ;
Haefliger, JA ;
Mooser, V ;
Bonny, C ;
Nicod, P ;
Waeber, G .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (21) :7256-7267
[5]   MicroRNA functions in animal development and human disease [J].
Alvarez-Garcia, I ;
Miska, EA .
DEVELOPMENT, 2005, 132 (21) :4653-4662
[6]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[7]   Expression of neuronal traits in pancreatic beta cells - Implication of neuron-restrictive silencing factor/repressor element silencing transcription factor, a neuron-restrictive silencer [J].
Atouf, F ;
Czernichow, P ;
Scharfmann, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (03) :1929-1934
[8]   Genome-wide analysis of repressor element 1 silencing transcription factor/neuron-restrictive silencing factor (REST/NRSF) target genes [J].
Bruce, AW ;
Donaldson, IJ ;
Wood, IC ;
Yerbury, SA ;
Sadowski, MI ;
Chapman, M ;
Göttgens, B ;
Buckley, NJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (28) :10458-10463
[9]   Expression profiling of palmitate- and oleate-regulated genes provides novel insights into the effects of chronic lipid exposure on pancreatic β-cell function [J].
Busch, AK ;
Cordery, D ;
Denyer, GS ;
Biden, TJ .
DIABETES, 2002, 51 (04) :977-987
[10]  
Calderone A, 2003, J NEUROSCI, V23, P2112