Evidence map›Paper›PMID 10891488›Full record

ArticleMolecular and cellular biology2000

Increased energy expenditure, decreased adiposity, and tissue-specific insulin sensitivity in protein-tyrosine phosphatase 1B-deficient mice.

L D Klaman, O Boss, O D Peroni, J K Kim, J L Martino, J M Zabolotny, N Moghal, M Lubkin, Y B Kim, A H Sharpe and 4 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 385 papers.

0numbers the graph read from it
0cells of the map it votes in
385citing papers in PubMed
18.2field-weighted citation impact, top 1% 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

385 citing papers in PubMed, 1,223 citations in OpenAlex.

  1. Review
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  12. Central leptin pathways in metabolic homeostasis.Clinical science (London, England : 1979) · 2025
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325 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 1 country.

L D KlamanCancer Biology Program, Division of Hematology-Oncology, Boston, Massachusetts 02215, USA.
O Boss
O D Peroni
J K Kim
J L Martino
J M Zabolotny
N Moghal
M Lubkin
Y B Kim
A H Sharpe
A Stricker-Krongrad
G I Shulman
B G Neel
B B Kahn
Millennium Engineering and Integration (United States) · USBrigham and Women's Hospital · USHoward Hughes Medical Institute · USYale University · US

Funding

Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Richard A Flavell · 1993 to 2026
$44.0M
Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI GREENBERG, ANDREW S, PERISSI, VALENTINA · 1992 to 2021
$25.0M
The Arcuate Nucleus: A Genetic Assessment of FunctionP01DK056116 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KAHN, BARBARA B. · 1999 to 2010
$15.6M
SIGNAL TRANSDUCTION PATHWAYS IN STABLE PHASE CHRONIC MYELOID LEUKEMIA CELLSP01DK050654 · NIDDK · DANA-FARBER CANCER INSTITUTE · PI D'ANDREA, ALAN DAVID · 1996 to 2006
$10.3M
Mechanisms of Lipid-Induced Hepatic Insulin ResistanceR01DK040936 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 1989 to 2015
$5.1M
SIGNAL TRANSDUCTION BY NON-TRANSMEMBRANE PTPSR01CA049152 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEEL, BENJAMIN G. · 1989 to 2020
$4.4M
GLUCOSE TRANSPORTER REGULATION IN OBESITY AND DIABETESR01DK043051 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KAHN, BARBARA B. · 1992 to 2020
$4.4M
CLONING &CHARACTERIZATION OF RAB4 INTERACTING PROTEINSF32DK009903 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ZABOLOTNY, JANICE · 1999 to 2001
$83k
CD22 ALLELE SPECIFIC DIFFERENCES IN B CELL SIGNALINGF32AI009815 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KLAMAN, LORI D · 1997 to 1999
–
NCI NIH HHS R01 CA049152NIAID NIH HHS AI09815NIAID NIH HHS F32 AI009815NIDDK NIH HHS DK09903NIDDK NIH HHS F32 DK009903NIDDK NIH HHS P01 DK050654NIDDK NIH HHS P01 DK056116NIDDK NIH HHS P01 DK 56116NIDDK NIH HHS P30 DK045735NIDDK NIH HHS P30 DK046200NIDDK NIH HHS R01 DK040936NIDDK NIH HHS R01 DK043051
6 · The paper itself

Abstract

Protein-tyrosine phosphatase 1B (PTP-1B) is a major protein-tyrosine phosphatase that has been implicated in the regulation of insulin action, as well as in other signal transduction pathways. To investigate the role of PTP-1B in vivo, we generated homozygotic PTP-1B-null mice by targeted gene disruption. PTP-1B-deficient mice have remarkably low adiposity and are protected from diet-induced obesity. Decreased adiposity is due to a marked reduction in fat cell mass without a decrease in adipocyte number. Leanness in PTP-1B-deficient mice is accompanied by increased basal metabolic rate and total energy expenditure, without marked alteration of uncoupling protein mRNA expression. In addition, insulin-stimulated whole-body glucose disposal is enhanced significantly in PTP-1B-deficient animals, as shown by hyperinsulinemic-euglycemic clamp studies. Remarkably, increased insulin sensitivity in PTP-1B-deficient mice is tissue specific, as insulin-stimulated glucose uptake is elevated in skeletal muscle, whereas adipose tissue is unaffected. Our results identify PTP-1B as a major regulator of energy balance, insulin sensitivity, and body fat stores in vivo.

Indexed as

Energy MetabolismMembrane Transport ProteinsMitochondrial ProteinsAdipose TissueAnimalsBody WeightCarrier ProteinsFemaleGlucoseGlucose Tolerance TestHomeostasisHyperinsulinismInsulin ResistanceIon ChannelsLeptinMaleCarrier ProteinsGlucoseIon ChannelsLeptinMembrane ProteinsMembrane Transport ProteinsMitochondrial ProteinsProteinsProtein Tyrosine Phosphatase, Non-Receptor Type 1Protein Tyrosine PhosphatasesPtpn1 protein, mouseRNA, MessengerUncoupling Protein 1Uncoupling Protein 2Uncoupling Protein 3

Identifiers

PMID10891488
PMCPMC85999
OpenAlexW2115681043

What OpenQuestion holds

Textmetadata
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.