Evidence map›Paper›PMID 23059889›Full record

ArticleHistology and histopathology2012

Nerve-Langerhans cell interactions in diabetes and aging.

A L N Doss, P G Smith

Abstract read
In one paragraph

Article in Histology and histopathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Peripheral Neuropathy in Mouse Models of Diabetes.Current protocols in mouse biology · 2016
    Review
  5. Article
  6. 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

2 authors at 1 institution in 1 country.

A L N DossDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
P G Smith
University of Kansas Medical Center · US

Funding

Research Design and Analysis Core (RDAC)P30HD002528 · NICHD · UNIVERSITY OF KANSAS LAWRENCE · PI FOWLER, STEPHEN CLETIUS · 1985 to 2015
$22.1M
Identifying therapeutic targets for vulvodyniaR01HD049615 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SMITH, PETER G · 2006 to 2016
$3.2M
Mechanisms of Sympathetic Axon PruningR01NS053796 · NINDS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SMITH, PETER G · 2007 to 2010
$1.3M
The Effects of Estrogen on the Progression of Diabetic Peripheral NeuropathyF31DK083845 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DOSS, ARGENIA L N · 2008 to 2009
$50k
NICHD NIH HHS P30 HD002528NICHD NIH HHS R01 HD049615NIDDK NIH HHS 1F31 DK083845NIDDK NIH HHS F31 DK083845NINDS NIH HHS 1R01 NS053796NINDS NIH HHS R01 NS053796
6 · The paper itself

Abstract

Cutaneous infections are a leading cause of hospitalization of diabetic patients. Langerhans cells (LCs) are antigen-presenting cutaneous dendritic cells that protect against infections, and effects of diabetes and aging on these cells are unclear. We examined LCs in footpads of rats with streptozotocin-induced diabetes at 3 months of age following 4 weeks of diabetes, and at 6 months following 16 weeks of diabetes. Immunostaining of LCs using the selective marker protein langerin showed cutaneous LC composition increased between 3 and 6 months of age owing to increased LC numbers and size in control rats. In diabetic rats, LC numbers increased with age but, unlike 6 month old controls, cell size did not, suggesting that diabetes impairs the increase in cell size that is a hallmark of LC maturation. Diabetes reduced LC numbers after 4 weeks and numbers and sizes following 16 weeks. We examined the relation between LC and innervation and found that, while axon density decreased with aging, it was not affected by 16 weeks of diabetes. However, LCs expressing the neuronal marker PGP9.5 represented a source of error in axonal counts. These findings support the hypothesis that diabetes substantially impacts LC proliferation and maturation independent of effects on cutaneous innervation. Accordingly, the interactions of diabetes and aging on LCs may be important factors in predisposing diabetic patients to cutaneous ulcers and infections.

Indexed as

AgingAnimalsAntigens, SurfaceCell DifferentiationCell ProliferationDiabetes ComplicationsDiabetes MellitusDiabetes Mellitus, ExperimentalFemaleHumansImmunohistochemistryLangerhans CellsNerve FibersNeuronsRatsRats, Sprague-DawleyAntigens, SurfaceUbiquitin ThiolesteraseUCHL1 protein, rat

Identifiers

PMID23059889
PMCPMC3714397
OpenAlexW1631423768

What OpenQuestion holds

Textmetadata
LicenceTDM
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.