期刊
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 22, 期 21, 页码 -出版社
MDPI
DOI: 10.3390/ijms222111675
关键词
AMP-activated protein kinase; AMPK; mTORC1; mitochondrial biogenesis; mitochondrial phosphoproteome; phosphoproteomics; Dictyostelium discoideum
资金
- Alexander von Humboldt Foundation
- PRIME-XS Consortium (seventh Framework Programme of the European Union) [262067-PRIME-XS]
Mitochondrial biogenesis is a tightly regulated process dependent on various signaling pathways that respond to cellular and environmental cues. AMPK plays a crucial role in maintaining cellular energy homeostasis and has been shown to regulate mitochondrial biogenesis, although the molecular mechanisms are not fully understood. Overexpression of AMPK in D. discoideum enhances mitochondrial biogenesis while impacting cell growth and development. Proteomics analysis reveals changes in phosphorylation levels and abundance of proteins related to energy metabolism, protein synthesis, and inner membrane biogenesis in response to AMPK overexpression, suggesting an interplay between AMPK and mTORC1 signaling pathways in controlling cellular growth and mitochondrial biogenesis.
Mitochondrial biogenesis is a highly controlled process that depends on diverse signalling pathways responding to cellular and environmental signals. AMP-activated protein kinase (AMPK) is a critical metabolic enzyme that acts at a central control point in cellular energy homeostasis. Numerous studies have revealed the crucial roles of AMPK in the regulation of mitochondrial biogenesis; however, molecular mechanisms underlying this process are still largely unknown. Previously, we have shown that, in cellular slime mould Dictyostelium discoideum, the overexpression of the catalytic alpha subunit of AMPK led to enhanced mitochondrial biogenesis, which was accompanied by reduced cell growth and aberrant development. Here, we applied mass spectrometry-based proteomics of Dictyostelium mitochondria to determine the impact of chronically active AMPK alpha on the phosphorylation state and abundance of mitochondrial proteins and to identify potential protein targets leading to the biogenesis of mitochondria. Our results demonstrate that enhanced mitochondrial biogenesis is associated with variations in the phosphorylation levels and abundance of proteins related to energy metabolism, protein synthesis, transport, inner membrane biogenesis, and cellular signalling. The observed changes are accompanied by elevated mitochondrial respiratory activity in the AMPK overexpression strain. Our work is the first study reporting on the global phosphoproteome profiling of D. discoideum mitochondria and its changes as a response to constitutively active AMPK. We also propose an interplay between the AMPK and mTORC1 signalling pathways in controlling the cellular growth and biogenesis of mitochondria in Dictyostelium as a model organism.
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