Evidence map›Paper›PMID 20498061›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Conserved role for autophagy in Rho1-mediated cortical remodeling and blood cell recruitment.

Pavan Kadandale, Joshua D Stender, Christopher K Glass, Amy A Kiger

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.0field-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

40 citing papers in PubMed, 64 citations in OpenAlex.

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  13. The Multifaceted Effects of Autophagy on the Tumor Microenvironment.Advances in experimental medicine and biology · 2020
    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

4 authors at 1 institution in 1 country.

Pavan KadandaleSection of Cell & Developmental Biology and Departments of Cellular and Molecular Medicine and Medicine, University of California, San Diego, CA 92093, USA.
Joshua D Stender
Christopher K Glass
Amy A Kiger
University of California, San Diego · US

Funding

STEROL LIPIDSU54GM069338 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DENNIS, EDWARD A · 2003 to 2013
$72.2M
Contemporary Approaches to Cancer Cell Signaling and CommunicationT32CA009523 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DONOGHUE, DANIEL J, YANG, JING · 1985 to 2025
$12.1M
U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
SECRETION AND GOLGI TRAFFIC IN PITUITARY AND OTHER CELLSR01DK017780 · NIDDK · YALE UNIVERSITY · PI FARQUHAR, MARILYN GIST · 1986 to 2010
$3.7M
Function of Myotubularin Phosphoinositide Phosphatase in MorphogenesisR01GM078176 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KIGER, AMY A · 2007 to 2012
$1.6M
SECRETION AND GOLGI TRAFFIC IN PITUITARY AND OTHER CELLSR37DK017780 · NIDDK · YALE UNIVERSITY · PI FARQUHAR, MARILYN GIST · 1988 to 1995
–
NCI NIH HHS T32 CA009523NIDDK NIH HHS DK17780NIDDK NIH HHS R01 DK017780NIGMS NIH HHS R01 GM078176NIGMS NIH HHS U54 GM069338NINDS NIH HHS P30 NS047101
6 · The paper itself

Abstract

Dynamic regulation of cell shape underlies many developmental and immune functions. Cortical remodeling is achieved under the central control of Rho GTPase pathways that modulate an exquisite balance in the dynamic assembly and disassembly of the cytoskeleton and focal adhesions. Macroautophagy (autophagy), associated with bulk cytoplasmic remodeling through lysosomal degradation, has clearly defined roles in cell survival and death. Moreover, it is becoming apparent that proteins, organelles, and pathogens can be targeted for autophagic clearance by selective mechanisms, although the extent and roles of such degradation are unclear. Here we report a conserved role for autophagy specifically in the cortical remodeling of Drosophila blood cells (hemocytes) and mouse macrophages. Continuous autophagy was required for integrin-mediated hemocyte spreading and Rho1-induced cell protrusions. Consequently, hemocytes disrupted for autophagy were impaired in their recruitment to epidermal wounds. Cell spreading required ref(2)P, the Drosophila p62 multiadaptor, implicating selective autophagy as a novel mechanism for modulating cortical dynamics. These results illuminate a specific and conserved role for autophagy as a regulatory mechanism for cortical remodeling, with implications for immune cell function.

Indexed as

AutophagyAnimalsAutophagy-Related Protein-1 HomologCell AdhesionCells, CulturedCell SurvivalDrosophila melanogasterDrosophila ProteinsHemocytesMacrophagesMiceProtein Serine-Threonine Kinasesrho GTP-Binding ProteinsAtg1 protein, DrosophilaAutophagy-Related Protein-1 HomologDrosophila ProteinsProtein Serine-Threonine KinasesRho1 protein, Drosophilarho GTP-Binding Proteins

Identifiers

PMID20498061
PMCPMC2890812
OpenAlexW1999203398

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.