Cell differentiation within a yeast colony: metabolic and regulatory parallels with a tumor-affected organism
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
55005623
Howard Hughes Medical Institute - United States
PubMed
22560924
DOI
10.1016/j.molcel.2012.04.001
PII: S1097-2765(12)00266-3
Knihovny.cz E-zdroje
- MeSH
- aminokyseliny metabolismus MeSH
- autofagie MeSH
- biologické modely MeSH
- buněčné dělení MeSH
- fyziologický stres MeSH
- genový knockout MeSH
- geny hub MeSH
- kvartérní amoniové sloučeniny metabolismus MeSH
- lidé MeSH
- metabolické sítě a dráhy MeSH
- nádory metabolismus patologie MeSH
- Saccharomyces cerevisiae - proteiny genetika MeSH
- Saccharomyces cerevisiae cytologie genetika růst a vývoj metabolismus MeSH
- signální transdukce MeSH
- spotřeba kyslíku MeSH
- transkriptom MeSH
- transportní systémy aminokyselin genetika MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- aminokyseliny MeSH
- kvartérní amoniové sloučeniny MeSH
- Saccharomyces cerevisiae - proteiny MeSH
- transportní systémy aminokyselin MeSH
Nutrient sensing and metabolic reprogramming are crucial for metazoan cell aging and tumor growth. Here, we identify metabolic and regulatory parallels between a layered, multicellular yeast colony and a tumor-affected organism. During development, a yeast colony stratifies into U and L cells occupying the upper and lower colony regions, respectively. U cells activate a unique metabolism controlled by the glutamine-induced TOR pathway, amino acid-sensing systems (SPS and Gcn4p) and signaling from mitochondria with lowered respiration. These systems jointly modulate U cell physiology, which adapts to nutrient limitations and utilize the nutrients released from L cells. Stress-resistant U cells share metabolic pathways and other similar characteristics with tumor cells, including the ability to proliferate. L cells behave similarly to stressed and starving cells, which activate degradative mechanisms to provide nutrients to U cells. Our data suggest a nutrient flow between both cell types, resembling the Cori cycle and glutamine-NH(4)(+) shuttle between tumor and healthy metazoan cells.
Citace poskytuje Crossref.org
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GEO
GSE35887