Abstract
The identification, more than 50 years ago, of mitochondria as the site of oxidative energy metabolism has prompted studies that have unraveled the complexity of the numerous biosynthetic and degradative reactions, fundamental to cell function, carried out by these organelles. These activities depend on a distinctive mitochondrial structure, with different enzymes and reactions localized in discrete membranes and aqueous compartments. The characteristic mitochondrial structural organization is the product of both synthesis of macromolecules within the mitochondria and the import of proteins and lipids synthesized outside the organelle. Synthesis and import of mitochondrial components are required for mitochondrial proliferation, but rather than producing new organelles, these processes may facilitate the growth of pre-existing mitochondria. Recent evidence indicates that these events are regulated in a complex way by several agonists and environmental conditions, through activation of specific transcription factors and signaling pathways. Some of these are now being elucidated. Generation of nitric oxide (NO) appears to be a novel player in this scenario, possibly acting as a unifying molecular switch to trigger the whole mitochondriogenic process.
| Original language | English |
|---|---|
| Pages (from-to) | 1-15 |
| Number of pages | 15 |
| Journal | Biochemical Pharmacology |
| Volume | 67 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Jan 1 2004 |
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Keywords
- Cellular signaling
- Energy metabolism
- Mitochondrial biogenesis
ASJC Scopus subject areas
- Pharmacology
Cite this
Mitochondrial biogenesis as a cellular signaling framework. / Nisoli, Enzo; Clementi, Emilio; Moncada, Salvador; Carruba, Michele O.
In: Biochemical Pharmacology, Vol. 67, No. 1, 01.01.2004, p. 1-15.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Mitochondrial biogenesis as a cellular signaling framework
AU - Nisoli, Enzo
AU - Clementi, Emilio
AU - Moncada, Salvador
AU - Carruba, Michele O.
PY - 2004/1/1
Y1 - 2004/1/1
N2 - The identification, more than 50 years ago, of mitochondria as the site of oxidative energy metabolism has prompted studies that have unraveled the complexity of the numerous biosynthetic and degradative reactions, fundamental to cell function, carried out by these organelles. These activities depend on a distinctive mitochondrial structure, with different enzymes and reactions localized in discrete membranes and aqueous compartments. The characteristic mitochondrial structural organization is the product of both synthesis of macromolecules within the mitochondria and the import of proteins and lipids synthesized outside the organelle. Synthesis and import of mitochondrial components are required for mitochondrial proliferation, but rather than producing new organelles, these processes may facilitate the growth of pre-existing mitochondria. Recent evidence indicates that these events are regulated in a complex way by several agonists and environmental conditions, through activation of specific transcription factors and signaling pathways. Some of these are now being elucidated. Generation of nitric oxide (NO) appears to be a novel player in this scenario, possibly acting as a unifying molecular switch to trigger the whole mitochondriogenic process.
AB - The identification, more than 50 years ago, of mitochondria as the site of oxidative energy metabolism has prompted studies that have unraveled the complexity of the numerous biosynthetic and degradative reactions, fundamental to cell function, carried out by these organelles. These activities depend on a distinctive mitochondrial structure, with different enzymes and reactions localized in discrete membranes and aqueous compartments. The characteristic mitochondrial structural organization is the product of both synthesis of macromolecules within the mitochondria and the import of proteins and lipids synthesized outside the organelle. Synthesis and import of mitochondrial components are required for mitochondrial proliferation, but rather than producing new organelles, these processes may facilitate the growth of pre-existing mitochondria. Recent evidence indicates that these events are regulated in a complex way by several agonists and environmental conditions, through activation of specific transcription factors and signaling pathways. Some of these are now being elucidated. Generation of nitric oxide (NO) appears to be a novel player in this scenario, possibly acting as a unifying molecular switch to trigger the whole mitochondriogenic process.
KW - Cellular signaling
KW - Energy metabolism
KW - Mitochondrial biogenesis
UR - http://www.scopus.com/inward/record.url?scp=0345118055&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0345118055&partnerID=8YFLogxK
U2 - 10.1016/j.bcp.2003.10.015
DO - 10.1016/j.bcp.2003.10.015
M3 - Article
C2 - 14667924
AN - SCOPUS:0345118055
VL - 67
SP - 1
EP - 15
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
SN - 0006-2952
IS - 1
ER -