J 2016

Notch stimulates growth by direct regulation of genes involved in the control of glycolysis and the tricarboxylic acid cycle

SLANINOVA, Vera; Michaela KRAFČÍKOVÁ; Raquel PEREZ-GOMEZ; Pavel STEFFAL; Lukáš TRANTÍREK et al.

Základní údaje

Originální název

Notch stimulates growth by direct regulation of genes involved in the control of glycolysis and the tricarboxylic acid cycle

Autoři

SLANINOVA, Vera; Michaela KRAFČÍKOVÁ ORCID; Raquel PEREZ-GOMEZ; Pavel STEFFAL; Lukáš TRANTÍREK; Sarah J. BRAY a Alena KREJCI

Vydání

OPEN BIOLOGY, LONDON, ROYAL SOC, 2016, 2046-2441

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10600 1.6 Biological sciences

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 3.481

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14740/16:00093886

Organizační jednotka

Středoevropský technologický institut

EID Scopus

Klíčová slova anglicky

metabolism; Notch targets; Warburg effect; glycolytic shift; tissue growth

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 5. 2. 2021 12:38, Mgr. Michaela Dzurov Krafčíková, Ph.D.

Anotace

V originále

Glycolytic shift is a characteristic feature of rapidly proliferating cells, such as cells during development and during immune response or cancer cells, as well as of stem cells. It results in increased glycolysis uncoupled from mitochondrial respiration, also known as the Warburg effect. Notch signalling is active in contexts where cells undergo glycolytic shift. We decided to test whether metabolic genes are direct transcriptional targets of Notch signalling and whether upregulation of metabolic genes can help Notch to induce tissue growth under physiological conditions and in conditions of Notch-induced hyperplasia. We show that genes mediating cellular metabolic changes towards the Warburg effect are direct transcriptional targets of Notch signalling. They include genes encoding proteins involved in glucose uptake, glycolysis, lactate to pyruvate conversion and repression of the tricarboxylic acid cycle. The direct transcriptional upregulation of metabolic genes is PI3K/Akt independent and occurs not only in cells with overactivated Notch but also in cells with endogenous levels of Notch signalling and in vivo. Even a short pulse of Notch activity is able to elicit long-lasting metabolic changes resembling the Warburg effect. Loss of Notch signalling in Drosophila wing discs as well as in human microvascular cells leads to downregulation of glycolytic genes. Notch-driven tissue overgrowth can be rescued by downregulation of genes for glucose metabolism. Notch activity is able to support growth of wing during nutrient-deprivation conditions, independent of the growth of the rest of the body. Notch is active in situations that involve metabolic reprogramming, and the direct regulation of metabolic genes may be a common mechanism that helps Notch to exert its effects in target tissues.