PDK-1/FoxO1 pathway in POMC neurons regulates Pomc expression and food intake

Kristy Iskandar, Yongheng Cao, Yoshitake Hayashi, Masanori Nakata, Eisuke Takano, Toshihiko Yada, Changliang Zhang, Wataru Ogawa, Miyo Oki, Streamson Chua, Hiroshi Itoh, Tetsuo Noda, Masato Kasuga, Jun Nakae

研究成果: Article査読

53 被引用数 (Scopus)

抄録

Both insulin and leptin signaling converge on phosphatidylinositol 3-OH kinase [PI(3)K]/3-phosphoinositide-dependent protein kinase-1 (PDK-1)/protein kinase B (PKB, also known as Akt) in proopiomelanocortin (POMC) neurons. Forkhead box-containing protein-O1 (FoxO1) is inactivated in a PI(3)K-dependent manner. However, the interrelationship between PI(3)K/PDK-1/Akt and FoxO1, and the chronic effects of the overexpression of FoxO1 in POMC neurons on energy homeostasis has not been elucidated. To determine the extent to which PDK-1 and FoxO1 signaling in POMC neurons was responsible for energy homeostasis, we generated POMC neuron-specific Pdk1 knockout mice (POMCPdk1-/-) and mice selectively expressing a constitutively nuclear (CN)FoxO1 or transactivation-defective (Δ256)FoxO1 in POMC neurons (CNFoxO1 POMC or Δ256FoxO1POMC). POMCPdk1-/- mice showed increased food intake and body weight accompanied by decreased expression of Pomc gene. The CNFoxO1POMC mice exhibited mild obesity and hyperphagia compared with POMCPdk1-/- mice. Although expression of the CNFoxO1 made POMCPdk1-/- mice more obese due to excessive suppression of Pomc gene, overexpression of Δ256FoxO1 in POMC neurons had no effects on metabolic phenotypes and Pomc expression levels of POMCPdk1 -/- mice. These data suggest a requirement for PDK-1 and FoxO1 in transcriptional regulation of Pomc and food intake.

本文言語English
ページ(範囲)E787-E798
ジャーナルAmerican Journal of Physiology - Endocrinology and Metabolism
298
4
DOI
出版ステータスPublished - 2010 4月

ASJC Scopus subject areas

  • 内分泌学、糖尿病および代謝内科学
  • 生理学
  • 生理学(医学)

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