Nutrient sensing, metabolism, and cell growth control - PubMed (original) (raw)

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Nutrient sensing, metabolism, and cell growth control

Hai-Xin Yuan et al. Mol Cell. 2013.

Abstract

Cell growth is regulated by coordination of both extracellular nutrients and intracellular metabolite concentrations. AMP-activated kinase and mammalian target of rapamycin complex 1 serve as key molecules that sense cellular energy and nutrients levels, respectively. In addition, the members of the dioxygenase family, including prolylhydroxylase, lysine demethylase, and DNA demethylase, have emerged as possible sensors of intracellular metabolic status. The interplay among nutrients, metabolites, gene expression, and protein modification are involved in the coordination of cell growth with extracellular and intracellular conditions.

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Figures

Figure 1

Figure 1

Nutrient sensing and metabolism pathways. AMP-activated kinase (AMPK) is activated by energy stress and promotes catabolic pathways to produce ATP while switching off ATP-consuming anabolic pathways. In contrast, mammalian target of rapamycin complex 1 (mTORC1) activation under nutrient-sufficiency leads to significant elevation of anabolic processes, such as protein and lipid synthesis. Abbreviations are: GLU4, glucose transporter type 4; CPT1, Carnitine Palmitoyltransferase-1; TAK1, TGFβ-activated kinase 1; LKB1, liver kinase B1 (a key AMPK activator tumor suppressor); CAMKKβ, Calmodulin-dependent protein kinase kinase β; ACC, acetyl CoA carboxylase; PFK2, Phosphofructokinase 2; GS, glycogen synthase; HDACs, histone deacetylases; CRTC2, CREB-regulated transcription co-activator 2; FOXO, forkhead box protein O; CREB, cAMP response element-binding protein; ULK, UNC-51-like kinase; FIP200, 200 kDa FAK family kinase-interacting protein; ATG, autophagy-related; PI3K, phosphoinositide 3-kinase; IRS1, insulin receptor substrate 1; PTEN, phosphatase and tensin homologue; PDK1, 3-phosphoinositide-dependent protein kinase 1; TSC1/2, tuberous sclerosis 1/2; Rheb, Ras homologue enriched in brain; v-ATPase, vacuolar H+-adenosine triphosphatase; 4E-BP1, eukaryotic initiation factor 4E-binding protein 1; S6K, ribosomal S6 kinase; Ragulator, a protein complex responsible for lysosomal recruitment and activation of Rag GTPases; PGC1α, peroxisome proliferator-activated receptor-γ coactivator 1α; PPARγ, peroxisome proliferator-activated receptor-γ; SREBP, sterol regulatory element-binding protein; HIF, Hypoxia-inducible factors. Stimulatory interactions are indicated with ↓ and inhibitory interactions are indicated with ⊥.

Figure 2

Figure 2

Dioxygenases in sensing metabolic intermediates and epigenetic regulation. (A) Schematics of α-KG metabolism and TCA cycle. The mutant isocitrate dehydrogenase (IDH) (indicated with a star) may decrease α-KG and generate a new oncometabolite 2-hydroxylglutarate (2-HG). (B) A proposed role of dioxygenases in metabolite sensing and epigenetic modifications. Using α-KG as a key substrate, dioxygenases is involved in HIFα hydroxylation, DNA demethylation, and histone demethylation. All processes are inhibited by normal metabolites, such as succinate and fumarate, as well as oncometabolite 2-HG. α-KG, α-ketoglutarate; GDH, glutamate dehydrogenase; SDH, succinate dehydrogenase; FH, fumarase; TET, ten-eleven translocation; KDM, lysine demethylase; PHD, prolyl hydroxylase domain protein.

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