Evidence map›Paper›PMID 30423168›Full record

ArticleJournal of molecular cell biology2018

Lztfl1/BBS17 controls energy homeostasis by regulating the leptin signaling in the hypothalamic neurons.

Qun Wei, Yi-Feng Gu, Qing-Jun Zhang, Helena Yu, Yan Peng, Kevin W Williams, Ruitao Wang, Kajiang Yu, Tiemin Liu, Zhi-Ping Liu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Central leptin pathways in metabolic homeostasis.Clinical science (London, England : 1979) · 2025
    Review
  2. Article
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  5. Metabolic consequences of skeletal muscle- and liver-specific BBSome deficiency.American journal of physiology. Endocrinology and metabolism · 2023
    Article
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  7. Article
  8. Review
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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

10 authors at 5 institutions in 2 countries.

Qun WeiDepartment of Surgical Oncology and Institute of Clinical Medicine, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Yi-Feng GuDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Qing-Jun ZhangDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Helena YuDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Yan PengDepartment of Pathology, UT Southwestern Medical Center, Dallas, TX, USA.
Kevin W WilliamsDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Ruitao WangDepartment of Intensive Care Unit, The Third Affiliated Hospital, Harbin Medical University, Harbin, China.
Kajiang YuDepartment of Intensive Care Unit, The Third Affiliated Hospital, Harbin Medical University, Harbin, China.
Tiemin LiuSate Key Laboratory of Genetic Engineering, School of Life Sciences, Department of Endocrinology and Metabolism, Zhongshan Hospital, Collaborative Innovation Center for Genetics and Development, Fudan University, Shanghai, China.
Zhi-Ping LiuDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Southwestern Medical Center · USHarbin Medical University · CNSouthwestern Medical CenterState Key Laboratory of Genetic EngineeringThe University of Texas Southwestern Medical Center · US

Funding

Targeting KDM4B, a novel alternative splicing regulator, in castration-resistant prostate cancer (CRPC)R01CA215063 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HSIEH, JER-TSONG, LIU, ZHI-PING · 2018 to 2022
$1.9M
Epigenetic Regulation of Cardiac Hypertrophy and Heart FailureR01HL109471 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI LIU, ZHI-PING · 2012 to 2015
$1.6M
NCI NIH HHS R01 CA215063NHLBI NIH HHS R01 HL109471
6 · The paper itself

Abstract

Leptin receptor (LepRb) signaling pathway in the hypothalamus of the forebrain controls food intake and energy expenditure in response to an altered energy state. Defects in the LepRb signaling pathway can result in leptin-resistance and obesity. Leucine zipper transcription factor like 1 (Lztfl1)/BBS17 is a member of the Bardet-Biedl syndrome (BBS) gene family. Human BBS patients have a wide range of pathologies including obesity. The cellular and molecular mechanisms underlying Lztfl1-regulated obesity are unknown. Here, we generated Lztfl1f/f mouse model in which Lztfl1 can be deleted globally and in tissue-specific manner. Global Lztfl1 deficiency resulted in pleiotropic phenotypes including obesity. Lztfl1-/- mice are hyperphagic and showed similar energy expenditure as WT littermates. The obese phenotype of Lztfl1-/- mice is caused by the loss of Lztfl1 in the brain but not in the adipocytes. Lztfl1-/- mice are leptin-resistant. Inactivation of Lztfl1 abolished phosphorylation of Stat3 in the LepRb signaling pathway in the hypothalamus upon leptin stimulation. Deletion of Lztfl1 had no effect on LepRb membrane localization. Furthermore, we observed that Lztfl1-/- mouse embryonic fibroblasts (MEFs) have significantly longer cilia than WT MEFs. We identified several proteins that potentially interact with Lztfl1. As these proteins are known to be involved in regulation of actin/cytoskeleton dynamics, we suggest that Lztfl1 may regulate leptin signaling and ciliary structure via these proteins. Our study identified Lztfl1 as a novel player in the LepRb signaling pathway in the hypothalamus that controls energy homeostasis.

Indexed as

AnimalsBardet-Biedl SyndromeCiliaCytoskeletonDisease Models, AnimalEnergy MetabolismFemaleFibroblastsHypothalamusLeptinMaleMice, Inbred C57BLMice, Mutant StrainsObesityProsencephalonReceptors, LeptinLeptinleptin receptor, mouseLztfl1 protein, mouseReceptors, LeptinTranscription Factors

Identifiers

PMID30423168
PMCPMC7191877
OpenAlexW2789668408

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.