Evidence map›Paper›PMID 16439805›Full record

ArticleAmerican journal of respiratory cell and molecular biology2006

Early emphysema in the tight skin and pallid mice: roles of microfibril-associated glycoproteins, collagen, and mechanical forces.

Satoru Ito, Erzsébet Bartolák-Suki, J Michael Shipley, Harikrishnan Parameswaran, Arnab Majumdar, Bélâ Suki

Open access · greenAbstract readComparative Study
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Increased Susceptibility to Glaucomatous Damage in Microfibril Deficient Mice.Investigative ophthalmology & visual science · 2020
    Article
  4. Article
  5. Article
  6. Review
  7. Proteoglycans maintain lung stability in an elastase-treated mouse model of emphysema.American journal of respiratory cell and molecular biology · 2014
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Acute mechanical forces cause deterioration in lung structure and function in elastase-induced emphysema.American journal of physiology. Lung cellular and molecular physiology · 2012
    Article
  13. Article
  14. Article
  15. Structure-function relations in an elastase-induced mouse model of emphysema.American journal of respiratory cell and molecular biology · 2011
    Article
  16. Lung parenchymal mechanics.Comprehensive Physiology · 2011
    Review
  17. Review
  18. Article
  19. Emergent structure-function relations in emphysema and asthma.Critical reviews in biomedical engineering · 2011
    Review
  20. Review
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

6 authors at 1 institution in 1 country.

Satoru ItoDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Erzsébet Bartolák-Suki
J Michael Shipley
Harikrishnan Parameswaran
Arnab Majumdar
Bélâ Suki
Boston University · US

Funding

Role of Mechanical Forces in the Progession of EmphysemaR01HL059215 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SUKI, BELA · 1998 to 2009
$2.8M
NHLBI NIH HHS HL 59215
6 · The paper itself

Abstract

The nature of the development of emphysema in the tight skin (Tsk) and the pallid (Pa) mice are not well understood. We assessed the mechanical and nonlinear properties of the respiratory system, the alveolar structure, and the levels of microfibril-associated glycoproteins (MAGP) 1 and 2 in Tsk mice with developmental emphysema; in Pa mice, which are thought to develop adult onset emphysema; and their background, the C57BL/6 mice, at an age of 7 wk. Minor differences between collagen-related elastic properties of the lungs of the Pa and C57BL/6 mice were seen at this early age. The lungs of the Tsk mice were significantly softer yet more nonlinear than those of the Pa and C57BL/6 mice. The MAGP-1 levels were similar in all three groups. However, the level of MAGP-2, which is associated with both fibrillin-1 and collagen, was higher in the Tsk than in the Pa mice, which also had more MAGP-2 than the C57BL/6. Both the mean and the variance of alveolar diameters were larger in the Tsk than in the other two groups, while the variance in the Pa was larger than in the C57BL/6 mice, implying early development of heterogeneity. Using a network model of the parenchyma, we linked the pathophysiologic changes in the Tsk mice to mechanical forces and failure of the alveolar walls. Our findings suggest the possibility that MAGP-2-related abnormal collagen assembly, combined with mechanical forces, is involved in the progression of emphysema in the Tsk mice.

Indexed as

Respiratory MechanicsAdipokinesAnimalsCollagenContractile ProteinsDisease Models, AnimalExtracellular Matrix ProteinsFibrillin-1FibrillinsLungLung ComplianceMiceMice, Inbred C57BLMice, Mutant StrainsMicrofilament ProteinsModels, BiologicalAdipokinesCollagenContractile ProteinsExtracellular Matrix ProteinsFbn1 protein, mouseFibrillin-1Fibrillinsmicrofibrillar proteinMicrofilament ProteinsRNA Splicing Factors

Identifiers

PMID16439805
PMCPMC2644230
OpenAlexW2005804802

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.