نتایج جستجو برای: factor forkhead box o1 foxo1

تعداد نتایج: 923682  

Journal: :FEBS Letters 2021

Glucagon antagonism has been reported as a new therapeutic approach to hyperglycaemia. As the 14-3-3 protein YWHAB identified regulator of glucagon receptor (GCGR) by affinity purification and mass spectrometry, we examined role in vivo. Ywhab knockout mice display impaired blood glucose homeostasis only under pyruvate stimulation. Deletion mouse primary hepatocytes (MPHs) increases hepatocyte ...

2016
Xiaochen Qu Zhongqiang Chen Dongwei Fan Chuiguo Sun Yan Zeng

Ossification of the ligamentum flavum (OLF) is a disorder of heterotopic ossification of spinal ligaments and is the main cause of thoracic spinal canal stenosis. Previous studies suggested that miR-132-3p negatively regulates osteoblast differentiation. However, whether miR-132-3p is involved in the process of OLF has not been investigated. In this study, we investigated the effect of miR-132-...

Journal: :The Biochemical journal 2010
Yoshihiro Yamazaki Yasutomi Kamei Satoshi Sugita Fumiko Akaike Sayaka Kanai Shinji Miura Yukio Hirata Bruce R Troen Tadahiro Kitamura Ichizo Nishino Takayoshi Suganami Osamu Ezaki Yoshihiro Ogawa

FOXO1 (forkhead box O1), a forkhead-type transcription factor whose gene expression is up-regulated in the skeletal muscle during starvation, appears to be a key molecule of energy metabolism and skeletal muscle atrophy. Cathepsin L, a lysosomal proteinase whose expression is also up-regulated in the skeletal muscle during starvation, is induced in transgenic mice overexpressing FOXO1 relative ...

2017
Meng Xu Xiaoling Chen Daiwen Chen Bing Yu Zhiqing Huang

FoxO1, a member of the forkhead transcription factor forkhead box protein O (FoxO) family, is predominantly expressed in most muscle types. FoxO1 is a key regulator of muscle growth, metabolism, cell proliferation and differentiation. In the past two decades, many researches have indicated that FoxO1 is a negative regulator of skeletal muscle differentiation while contrasting opinions consider ...

Journal: :The Journal of clinical investigation 2006
Michihiro Matsumoto Seongah Han Tadahiro Kitamura Domenico Accili

Hepatic insulin resistance affects both carbohydrate and lipid metabolism. It has been proposed that insulin controls these 2 metabolic branches through distinct signaling pathways. FoxO transcription factors are considered effectors of the pathway regulating hepatic glucose production. Here we show that adenoviral delivery of constitutively nuclear forkhead box O1 (FoxO1) to mouse liver result...

Journal: :Journal of cell science 2015
Yachen Shen Weifeng Xu Hui You Dongming Su Jing Xing Min Li Lei Li Xiubin Liang

The epithelial Na(+) channel (ENaC), regulated by insulin, is of fundamental importance in the control of Na(+) reabsorption in the distal nephron. The potential role of Forkhead box O1 (FoxO1), downstream of insulin signaling, in the regulation of ENaC remains to be investigated. Here, we found that the overexpression of a constitutively active form of FoxO1 (ADA-FoxO1) suppressed the mRNA lev...

2017
Dorina Ujvari Ivika Jakson Shabnam Babayeva Daniel Salamon Bence Rethi Sebastian Gidlöf Angelica Lindén Hirschberg

Insulin resistance and compensatory hyperinsulinemia are characteristic features of obesity and polycystic ovary syndrome, and both are associated with reduced fertility and implantation. There is little knowledge about the effect of insulin on the decidualization process and previous findings are contradictory. We investigated the effect of insulin on the regulation of forkhead box protein O1 ...

2012
Ana M. Mendes-Pereira Christopher J. Lord Alan Ashworth

PTEN (Phosphatase and tensin homolog) is a tumour suppressor gene commonly defective in human cancer, and is thus a potentially important therapeutic target. Targeting tumour suppressor loss-of-function is possible by exploiting the genetic concept of synthetic lethality (SL). By combining the use of isogenic models of PTEN deficiency with high-throughput RNA interference (RNAi) screening, we h...

2017
Paul J Brighton Yojiro Maruyama Katherine Fishwick Pavle Vrljicak Shreeya Tewary Risa Fujihara Joanne Muter Emma S Lucas Taihei Yamada Laura Woods Raffaella Lucciola Yie Hou Lee Satoru Takeda Sascha Ott Myriam Hemberger Siobhan Quenby Jan Joris Brosens

In cycling human endometrium, menstruation is followed by rapid estrogen-dependent growth. Upon ovulation, progesterone and rising cellular cAMP levels activate the transcription factor Forkhead box O1 (FOXO1) in endometrial stromal cells (EnSCs), leading to cell cycle exit and differentiation into decidual cells that control embryo implantation. Here we show that FOXO1 also causes acute senesc...

2015
Chenying Zhang Bhaskar Ponugoti Chen Tian Fanxing Xu Rohinton Tarapore Angelika Batres Sarah Alsadun Jason Lim Guangyu Dong Dana T. Graves

Healing is delayed in diabetic wounds. We previously demonstrated that lineage-specific Foxo1 deletion in keratinocytes interfered with normal wound healing and keratinocyte migration. Surprisingly, the same deletion of Foxo1 in diabetic wounds had the opposite effect, significantly improving the healing response. In normal glucose media, forkhead box O1 (FOXO1) enhanced keratinocyte migration ...

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