Evidence map›Paper›PMID 10233163›Full record

ArticleMolecular biology of the cell1999

Primary mesenchymal cells isolated from SPARC-null mice exhibit altered morphology and rates of proliferation.

A D Bradshaw, A Francki, K Motamed, C Howe, E H Sage

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular biology of the cell, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 93 citations in OpenAlex.

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  13. Regulator of Calcineurin 1 Isoform 4 (RCAN1.4) Is Overexpressed in the Glomeruli of Diabetic Mice.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2011
    Article
  14. SPARC: a matricellular regulator of tumorigenesis.Journal of cell communication and signaling · 2009
    Article
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  19. Critical roles of the guanylyl cyclase B receptor in endochondral ossification and development of female reproductive organs.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
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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

5 authors at 2 institutions in 1 country.

A D BradshawDepartment of Biological Structure, University of Washington, Seattle, Washington 98195, USA.
A Francki
K Motamed
C Howe
E H Sage
University of Washington · USThe Wistar Institute · US

Funding

VLA-4 and VCAM-1 in Advanced AtherosclerosisP01HL018645 · NHLBI · UNIVERSITY OF WASHINGTON · PI HARLAN, JOHN MARSHALL · 1985 to 2010
$23.9M
RESEARCH TRAINING IN RENAL DISEASET32DK007467 · NIDDK · UNIVERSITY OF WASHINGTON · PI BANSAL, NISHA, KESTENBAUM, BRYAN R · 1986 to 2023
$5.1M
EXTRACELLULAR PROTEINS AS SIGNALS IN ENDOTHELIAL GROWTHR01GM040711 · NIGMS · UNIVERSITY OF WASHINGTON · PI SAGE, EMILY HELENE · 1988 to 2009
$2.7M
COLLAGEN I AND ANGIOGENESIS AND VIVOF32GM018705 · NIGMS · UNIVERSITY OF WASHINGTON · PI BRADSHAW, AMY DODD · 1997 to 1998
–
NHLBI NIH HHS HL-18645NHLBI NIH HHS P01 HL018645NIDDK NIH HHS DK-47459NIDDK NIH HHS T32 DK007467NIGMS NIH HHS F32 GM018705NIGMS NIH HHS GM-40711NIGMS NIH HHS R01 GM040711
6 · The paper itself

Abstract

SPARC (secreted protein acidic and rich in cysteine)/BM 40/osteonectin is a matricellular protein shown to function as a counteradhesive factor that induces cell rounding and as an inhibitor of cell proliferation. These activities have been defined in cell culture, in which interpretation has been complicated by the presence of endogenous SPARC. We therefore sought to determine whether cell shape and proliferation would be affected by the absence of SPARC. Mesangial cells, fibroblasts, and aortic smooth muscle cells were isolated from SPARC-null and age-matched, wild-type mice. In contrast to wild-type cells, SPARC-null mesangial cells exhibited a flat morphology and an altered actin cytoskeleton. In addition, vinculin-containing focal adhesions were distributed over the center of SPARC-null cells, whereas in wild-type cells, the number of focal adhesions was reduced, and these structures were restricted largely to the cell periphery. Although the SPARC-null fibroblasts did not display overt differences in cell morphology, the cells responded to exogenous recombinant SPARC by rounding up in a manner similar to that of wild-type fibroblasts. Thus, the expression of endogenous SPARC is not required for the response of cells to SPARC. Additionally, SPARC-null mesangial cells, fibroblasts, and smooth muscle cells proliferated faster than their respective wild-type counterparts. Null cells also showed a greater sensitivity to the inhibition of cell cycle progression by the addition of recombinant SPARC. The increased proliferation rate of SPARC-null cells appeared to be mediated, at least in part, by an increase in the cell cycle regulatory protein cyclin A. We conclude that the expression of SPARC influences the cellular architecture of mesangial cells and that SPARC plays a role in the regulation of cell cycle in mesangial cells, fibroblasts, and smooth muscle cells.

Indexed as

AnimalsCell CycleCell DivisionCell SizeFibroblastsKidneyMesodermMiceMice, Inbred C57BLMice, Inbred StrainsMice, Mutant StrainsMuscle, Smooth, VascularOsteonectinOsteonectin

Identifiers

PMID10233163
PMCPMC25344
OpenAlexW2146758511

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.