نتایج جستجو برای: ins 1 cells

تعداد نتایج: 3783999  

Journal: :American journal of physiology. Endocrinology and metabolism 2012
Shenghao Liu Rui Liu Yu-Ting Chiang Lifang Song Xiaoming Li Tianru Jin Qinghua Wang

Insulin therapy using insulin detemir (d-INS) has demonstrated weight-sparing effects compared with other insulin formulations. Mechanisms underlying these effects, however, remain largely unknown. Here we postulate that the intestinal tissues' selective preference allows d-INS to exert enhanced action on proglucagon (Gcg) expression and the production of glucagon-like peptide (GLP)-1, an incre...

Journal: :Blood 1956
T TAKEUCHI K KINOSHITA

By TADAO rfAKEUCHI AND KENJI KIN0SHITA I N PREVIOUS STIJI)IES Takeuchi et al.’5 have showni that anssylophosphorylase could be demisonsstrated ins humisams amid ansimal tissue by histochemical nieanss. They did this by using the specific staimsimsg reactions of polysaccharide niewly fornssed frons glucose-i-phosphate as a result of emizynse activity. The presemsce of the enizyme was dennomistra...

Journal: :Cardiovascular research 2009
Ersilia Cipolletta Alfonso Campanile Gaetano Santulli Emma Sanzari Dario Leosco Pietro Campiglia Bruno Trimarco Guido Iaccarino

AIMS Insulin (Ins) resistance (IRES) associates to increased cardiovascular risk as observed in metabolic syndrome. Chronic stimulation of beta-adrenergic receptors (betaAR) due to exaggerated sympathetic nervous system activity is involved in the pathogenesis of IRES. The cellular levels of G protein coupled receptor kinase 2 (GRK2) increase during chronic betaAR stimulation, leading to betaAR...

Journal: :Current Biology 2008
Jennifer Mitchell Xueqing Wang Guangping Zhang Martina Gentzsch Deborah J. Nelson Stephen B. Shears

Ins(3,4,5,6)P(4) inhibits plasma membrane Cl(-) flux in secretory epithelia [1]. However, in most other mammalian cells, receptor-dependent elevation of Ins(3,4,5,6)P(4) levels is an "orphan" response that lacks biological significance [2]. We set out to identify Cl(-) channel(s) and/or transporter(s) that are regulated by Ins(3,4,5,6)P4 in vivo. Several candidates [3-5] were excluded through b...

Journal: :The Journal of clinical investigation 1998
H E Hohmeier A Thigpen V V Tran R Davis C B Newgard

The fact that insulin-producing islet beta-cells are susceptible to the cytotoxic effects of inflammatory cytokines represents a potential hinderance to the use of such cells for transplantation therapy of insulin-dependent diabetes mellitus (IDDM). In the current study, we show that IL-1beta induces destruction of INS-1 insulinoma cells, while having no effect on a second insulinoma cell line ...

Journal: :The Journal of biological chemistry 1993
M Neerman-Arbez P A Halban

Proinsulin is converted to equimolar amounts of insulin and connecting peptide (C-peptide) in pancreatic beta cell secretory granules. The fate of C-peptide, which remains soluble in granules while insulin is crystallized, was studied in a rat insulinoma cell line (INS cells). A pulse-chase approach demonstrated that insulin to C-peptide ratios (I/CP) began to rise in INS cells as soon as conve...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Sinisa Hrvatin Charles W O'Donnell Francis Deng Jeffrey R Millman Felicia Walton Pagliuca Philip DiIorio Alireza Rezania David K Gifford Douglas A Melton

Human pluripotent stem cells (hPSCs) have the potential to generate any human cell type, and one widely recognized goal is to make pancreatic β cells. To this end, comparisons between differentiated cell types produced in vitro and their in vivo counterparts are essential to validate hPSC-derived cells. Genome-wide transcriptional analysis of sorted insulin-expressing (INS(+)) cells derived fro...

Journal: :Diabetes 2004
Xiao Yu Koji Murao Yoshitaka Sayo Hitomi Imachi Wen M Cao Shouji Ohtsuka Michio Niimi Hiroshi Tokumitsu Hiroyuki Inuzuka Norman C W Wong Ryoji Kobayashi Toshihiko Ishida

A number of factors have been reported to affect insulin synthesis in beta-cells. Although glucose is the most important regulator of insulin gene expression in pancreatic beta-cells, the mechanisms whereby glucose stimulates insulin gene transcription in response to changes in glucose concentration have not been clarified yet. In this study, we examined the role of the Ca(2+)/calmodulin (CaM)-...

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