Evidence map›Paper›PMID 21521782›Full record

ArticleBlood2011

TIMP-1 deficiency subverts cell-cycle dynamics in murine long-term HSCs.

Lara Rossi, Aysegul V Ergen, Margaret A Goodell

Abstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Molecular regulation of hematopoietic stem cell quiescence.Cellular and molecular life sciences : CMLS · 2022
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Cytokine functions of TIMP-1.Cellular and molecular life sciences : CMLS · 2014
    Review
  9. Review
  10. Article
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

3 authors at 2 institutions in 2 countries.

Lara RossiCenter for Cell and Gene Therapy and Center for Stem Cells and Regenerative Medicine, Baylor College of Medicine, One Baylor Plaza,Houston, TX 77030, USA. lararossi79@yahoo.it
Aysegul V Ergen
Margaret A Goodell
Baylor College of Medicine · USUniversity of Bologna · IT

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Validation of Suicide Strategies for Cellular TherapyU54HL081007 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI BRENNER, MALCOLM K. · 2005 to 2009
$10.2M
REGULATION OF HEMATOPOIETIC PROGENITORS BY DE NOVO DNA METHYLATIONR01DK092883 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI GOODELL, MARGARET A. · 2012 to 2024
$7.4M
Tissue Engineering of Hematopoietic BoneR01EB005173 · NIBIB · BAYLOR COLLEGE OF MEDICINE · PI HIRSCHI, KAREN KEMPER · 2005 to 2009
$5.9M
MUSCLE-DERIVED HEMATOPOIETIC STEM CELLSR01DK058192 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI GOODELL, MARGARET A. · 2000 to 2010
$3.6M
NCI NIH HHS P30 CA125123NHLBI NIH HHS HL081007NHLBI NIH HHS U54 HL081007NIBIB NIH HHS EB005173NIBIB NIH HHS R01 EB005173NIDDK NIH HHS DK58192NIDDK NIH HHS R01 DK058192NIDDK NIH HHS R01 DK092883
6 · The paper itself

Abstract

In addition to the well-recognized role in extracellular matrix remodeling, the tissue inhibitor of metalloproteinases-1 (TIMP-1) has been suggested to be involved in the regulation of numerous biologic functions, including cell proliferation and survival. We therefore hypothesized that TIMP-1 might be involved in the homeostatic regulation of HSCs, whose biologic behavior is the synthesis of both microenvironmental and intrinsic cues. We found that TIMP-1(-/-) mice have decreased BM cellularity and, consistent with this finding, TIMP-1(-/-) HSCs display reduced capability of long-term repopulation. Interestingly, the cell cycle distribution of TIMP-1(-/-) stem cells appears distorted, with a dysregulation at the level of the G(1) phase. TIMP-1(-/-) HSCs also display increased levels of p57, p21, and p53, suggesting that TIMP-1 could be intrinsically involved in the regulation of HSC cycling dynamics. Of note, TIMP-1(-/-) HSCs present decreased levels of CD44 glycoprotein, whose expression has been proven to be controlled by p53, the master regulator of the G(1)/S transition. Our findings establish a role for TIMP-1 in regulating HSC function, suggesting a novel mechanism presiding over stem cell quiescence in the framework of the BM milieu.

Indexed as

AnimalsBone Marrow CellsBone Marrow TransplantationCell CycleCell ProliferationCells, CulturedHematopoietic Stem CellsKineticsMiceMice, Inbred C57BLMice, KnockoutModels, BiologicalTime FactorsTissue Inhibitor of Metalloproteinase-1Tissue Inhibitor of Metalloproteinase-1

Identifiers

PMID21521782
PMCPMC3123018
OpenAlexW2089235117

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.