Evidence map›Paper›PMID 24944899›Full record

ArticleMolecular metabolism2014

Rictor/mTORC2 facilitates central regulation of energy and glucose homeostasis.

Heidi E Kocalis, Scott L Hagan, Leena George, Maxine K Turney, Michael A Siuta, Gloria N Laryea, Lindsey C Morris, Louis J Muglia, Richard L Printz, Gregg D Stanwood and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.6field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 72 citations in OpenAlex.

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  12. Novel roles of mTORC2 in regulation of insulin secretion by actin filament remodeling.American journal of physiology. Endocrinology and metabolism · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Heidi E KocalisDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN, United States.
Scott L HaganVanderbilt University School of Medicine, Nashville, TN, United States.
Leena GeorgeDivision of Diabetes, Endocrinology and Metabolism, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, United States.
Maxine K TurneyDivision of Diabetes, Endocrinology and Metabolism, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, United States.
Michael A SiutaNeuroscience Graduate Program, Vanderbilt University, Nashville, TN, United States ; Vanderbilt University School of Medicine, Nashville, TN, United States.
Gloria N LaryeaNeuroscience Graduate Program, Vanderbilt University, Nashville, TN, United States.
Lindsey C MorrisDivision of Diabetes, Endocrinology and Metabolism, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, United States.
Louis J MugliaCenter for Prevention of Preterm Birth, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Richard L PrintzDepartment of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN, United States.
Gregg D StanwoodDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, United States.
Kevin D NiswenderDepartment of Veterans Affairs Tennessee Valley Healthcare System, Nashville, TN, United States ; Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN, United States ; Division of Diabetes, Endocrinology and Metabolism, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, United States.
Vanderbilt University · USUniversity of Cincinnati · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI MCGUINNESS, OWEN P · 1986 to 2011
$28.1M
MULTIDISCIPLINARY TRAINING IN MOLECULAR ENDOCRINOLOGYT32DK007563 · NIDDK · VANDERBILT UNIVERSITY · PI Richard M O'Brien · 1988 to 2026
$15.9M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Insulin Regulation of Monoamine Signaling: Pathway to ObesityR01DK085712 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GALLI, AURELIO, NISWENDER, KEVIN D · 2009 to 2013
$5.0M
EXPERIMENTAL ENDOCRINOLOGY AND METABOLISMT32DK007044 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Amit Majithia · 1986 to 2026
$4.6M
Vanderbilt Student Research Training ProgramT35DK007383 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI William Heerman · 1986 to 2026
$4.1M
Leptin and insulin action in the brain;role in obesityK08DK064857 · NIDDK · VANDERBILT UNIVERSITY · PI NISWENDER, KEVIN D · 2003 to 2007
$622k
CNS PPAR gamma and energy homeostasisF31DK083222 · NIDDK · VANDERBILT UNIVERSITY · PI KOCALIS, HEIDI E. · 2008 to 2011
$77k
NIDDK NIH HHS F31 DK083222NIDDK NIH HHS K08 DK064857NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS P60 DK020593NIDDK NIH HHS R01 DK085712NIDDK NIH HHS T32 DK007044NIDDK NIH HHS T32 DK007563NIDDK NIH HHS T35 DK007383NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

Insulin signaling in the central nervous system (CNS) regulates energy balance and peripheral glucose homeostasis. Rictor is a key regulatory/structural subunit of the mTORC2 complex and is required for hydrophobic motif site phosphorylation of Akt at serine 473. To examine the contribution of neuronal Rictor/mTORC2 signaling to CNS regulation of energy and glucose homeostasis, we utilized Cre-LoxP technology to generate mice lacking Rictor in all neurons, or in either POMC or AgRP expressing neurons. Rictor deletion in all neurons led to increased fat mass and adiposity, glucose intolerance and behavioral leptin resistance. Disrupting Rictor in POMC neurons also caused obesity and hyperphagia, fasting hyperglycemia and pronounced glucose intolerance. AgRP neuron specific deletion did not impact energy balance but led to mild glucose intolerance. Collectively, we show that Rictor/mTORC2 signaling, especially in POMC-expressing neurons, is important for central regulation of energy and glucose homeostasis.

Indexed as

AgRP neuronsCNS insulinEnergy balanceFood intakemTORC2ObesityPOMC neuronsRictor

Identifiers

PMID24944899
PMCPMC4060224
OpenAlexW2094677226

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.