Evidence map›Paper›PMID 30737382›Full record

ArticleNature communications2019

BMP-dependent synaptic development requires Abi-Abl-Rac signaling of BMP receptor macropinocytosis.

Najin Kim, Sungdae Kim, Minyeop Nahm, Danielle Kopke, Joohyung Kim, Eunsang Cho, Min-Jung Lee, Mihye Lee, Seung Hyun Kim, Kendal Broadie and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

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  13. Dysregulation of BMP, Wnt, and Insulin Signaling in Fragile X Syndrome.Frontiers in cell and developmental biology · 2022
    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

11 authors at 4 institutions in 4 countries.

Najin KimInterdisciplinary Graduate Program in Genetic Engineering, Seoul National University, Seoul, 08826, Korea.
Sungdae KimInterdisciplinary Graduate Program in Genetic Engineering, Seoul National University, Seoul, 08826, Korea.
Minyeop NahmDepartment of Neurology, Hanyang University College of Medicine, Seoul, 04763, Korea.
Danielle KopkeDepartments of Biological Sciences, Cell and Developmental Biology, and Pharmacology, Vanderbilt Brain Institute, Vanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, TN, 37232, USA.ORCID http://orcid.org/0000-0003-4326-3284
Joohyung KimDepartment of Brain and Cognitive Sciences, Seoul National University, Seoul, 08826, Korea.
Eunsang ChoDepartment of Brain and Cognitive Sciences, Seoul National University, Seoul, 08826, Korea.
Min-Jung LeeDepartment of Cell and Developmental Biology and Dental Research Institute, Seoul National University, Seoul, 08826, Korea.
Mihye LeeDepartment of Cell and Developmental Biology and Dental Research Institute, Seoul National University, Seoul, 08826, Korea.
Seung Hyun KimDepartment of Neurology, Hanyang University College of Medicine, Seoul, 04763, Korea.
Kendal BroadieDepartments of Biological Sciences, Cell and Developmental Biology, and Pharmacology, Vanderbilt Brain Institute, Vanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, TN, 37232, USA.
Seungbok LeeInterdisciplinary Graduate Program in Genetic Engineering, Seoul National University, Seoul, 08826, Korea. seunglee@snu.ac.kr.ORCID http://orcid.org/0000-0002-6620-6269
Seoul National University · KRSeoul National University Dental Hospital · KRVanderbilt University · USHanyang University · KR

Funding

Genetic and Developmental Analyses of Fragile X SyndromeR01MH084989 · NIMH · VANDERBILT UNIVERSITY · PI BROADIE, KENDAL · 2009 to 2021
$5.5M
Genetic Analysis of Synapse Formation and FunctionR01MH096832 · NIMH · VANDERBILT UNIVERSITY · PI BROADIE, KENDAL · 2012 to 2016
$2.3M
NIMH NIH HHS R01 MH084989NIMH NIH HHS R01 MH096832
6 · The paper itself

Abstract

Retrograde BMP trans-synaptic signaling is essential for synaptic development. Despite the importance of endocytosis-regulated BMP receptor (BMPR) control of this developmental signaling, the mechanism remains unknown. Here, we provide evidence that Abelson interactor (Abi), a substrate for Abl kinase and component of the SCAR/WAVE complex, links Abl and Rac1 GTPase signaling to BMPR macropinocytosis to restrain BMP-mediated synaptic development. We find that Abi acts downstream of Abl and Rac1, and that BMP ligand Glass bottom boat (Gbb) induces macropinocytosis dependent on Rac1/SCAR signaling, Abl-mediated Abi phosphorylation, and BMPR activation. Macropinocytosis acts as the major internalization route for BMPRs at the synapse in a process driven by Gbb activation and resulting in receptor degradation. Key regulators of macropinocytosis (Rabankyrin and CtBP) control BMPR trafficking to limit BMP trans-synaptic signaling. We conclude that BMP-induced macropinocytosis acts as a BMPR homeostatic mechanism to regulate BMP-mediated synaptic development.

Indexed as

AnimalsBone Morphogenetic Protein ReceptorsBone Morphogenetic ProteinsCarrier ProteinsDrosophilaDrosophila ProteinsGene Expression Regulation, DevelopmentalPhosphorylationProtein-Tyrosine Kinasesrac GTP-Binding ProteinsSignal TransductionSynapsesAbi protein, DrosophilaAbl protein, DrosophilaBone Morphogenetic Protein ReceptorsBone Morphogenetic ProteinsCarrier ProteinsDrosophila ProteinsProtein-Tyrosine Kinasesrac GTP-Binding Proteins

Identifiers

PMID30737382
PMCPMC6368546
OpenAlexW2912944509

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.