Evidence map›Paper›PMID 16314533›Full record

ArticleMolecular and cellular biology2005

periostin null mice exhibit dwarfism, incisor enamel defects, and an early-onset periodontal disease-like phenotype.

Hector Rios, Shrinagesh V Koushik, Haiyan Wang, Jian Wang, Hong-Ming Zhou, Andrew Lindsley, Rhonda Rogers, Zhi Chen, Manabu Maeda, Agnieszka Kruzynska-Frejtag and 2 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 204 papers.

0numbers the graph read from it
0cells of the map it votes in
204citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

204 citing papers in PubMed, 369 citations in OpenAlex.

  1. Article
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  6. Review
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  10. Temporal and spatial expression analysis of periostin in mice periodontitis model.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2024
    Article
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  13. Review
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  16. Article
  17. Periostin in Osteoporosis and Cardiovascular Disease.Journal of the Endocrine Society · 2023
    Review
  18. Article
  19. Article
  20. Article

144 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 3 countries.

Hector RiosCardiovascular Development Group, Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, 46202, USA.
Shrinagesh V Koushik
Haiyan Wang
Jian Wang
Hong-Ming Zhou
Andrew Lindsley
Rhonda Rogers
Zhi Chen
Manabu Maeda
Agnieszka Kruzynska-Frejtag
Jian Q Feng
Simon J Conway
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineUniversity of Missouri–Kansas City · USWroclaw Medical University · PL

Funding

MUCOPOLYSACCHRIDE METABOLISM IN CARDIAC ANOMALIESR01HL033756 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 1985 to 2015
$4.8M
NEURAL-CREST RELATED HEART DEFECTSR01HL060714 · NHLBI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI CONWAY, SIMON JAMES · 1998 to 2017
$4.7M
Pre and Post Doctoral Training: UMKC School of DentistryT32DE007294 · NIDCR · UNIVERSITY OF MISSOURI KANSAS CITY · PI EICK, J DAVID · 1996 to 2011
$4.4M
ROLES OF BMP4 &ITS REGULATION DURING TOOTH DEVELOPMENTR29DE013480 · NIDCR · UNIVERSITY OF MISSOURI KANSAS CITY · PI FENG, JIAN Q. · 1999 to 2003
$414k
MUCOPOLYSACCHARIDE METABOLISM IN CARDIAC ANOMALIESR37HL033756 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MARKWALD, ROGER R · 1987 to 1996
–
NHLBI NIH HHS HL33756NHLBI NIH HHS HL60714NHLBI NIH HHS R01 HL033756NHLBI NIH HHS R01 HL060714NIDCR NIH HHS DE13480NIDCR NIH HHS R29 DE013480NIDCR NIH HHS T32 DE007294NIDCR NIH HHS T32DE07294
6 · The paper itself

Abstract

Periostin was originally identified as an osteoblast-specific factor and is highly expressed in the embryonic periosteum, cardiac valves, placenta, and periodontal ligament as well as in many adult cancerous tissues. To investigate its role during development, we generated mice that lack the periostin gene and replaced the translation start site and first exon with a lacZ reporter gene. Surprisingly, although periostin is widely expressed in many developing organs, periostin-deficient (peri(lacZ)) embryos are grossly normal. Postnatally, however, approximately 14% of the nulls die before weaning and all of the remaining peri(lacZ) nulls are severely growth retarded. Skeletal analysis revealed that trabecular bone in adult homozygous skeletons was sparse, but overall bone growth was unaffected. Furthermore, by 3 months, the nulls develop an early-onset periodontal disease-like phenotype. Unexpectedly, these mice also show a severe incisor enamel defect, although there is no apparent change in ameloblast differentiation. Significantly, placing the peri(lacZ) nulls on a soft diet that alleviated mechanical strain on the periodontal ligament resulted in a partial rescue of both the enamel and periodontal disease-like phenotypes. Combined, these data suggest that a healthy periodontal ligament is required for normal amelogenesis and that periostin is critically required for maintenance of the integrity of the periodontal ligament in response to mechanical stresses.

Indexed as

Animalsbeta-GalactosidaseBone and BonesCell Adhesion MoleculesDental EnamelDwarfismFemaleGenes, ReporterIncisorInfertility, FemaleMaleMiceMice, Mutant StrainsPeriodontal DiseasesPhenotypebeta-GalactosidaseCell Adhesion MoleculesPostn protein, mouse

Identifiers

PMID16314533
PMCPMC1316984
OpenAlexW2101087657

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.