Evidence map›Paper›PMID 27328415›Full record

ArticleCellular reprogramming2016

Generation of Induced Pluripotent Stem Cells from Diabetic Foot Ulcer Fibroblasts Using a Nonintegrative Sendai Virus.

Behzad Gerami-Naini, Avi Smith, Anna G Maione, Olga Kashpur, Gianpaolo Carpinito, Aristides Veves, David J Mooney, Jonathan A Garlick

Abstract read
In one paragraph

Article in Cellular reprogramming, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Stem cell therapy in retinal diseases.Neural regeneration research · 2023
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Stem cell transplantation therapy for diabetic foot ulcer: a narrative review.Asian biomedicine : research, reviews and news · 2021
    Review
  11. Review
  12. Differentiation of diabetic foot ulcer-derived induced pluripotent stem cells reveals distinct cellular and tissue phenotypes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  13. Review
  14. iPSC technology-based regenerative therapy for diabetes.Journal of diabetes investigation · 2018
    Review
  15. 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

8 authors at 3 institutions in 1 country.

Behzad Gerami-Naini1 Department of Diagnostic Sciences, School of Dental Medicine, Tufts University , Boston, Massachusetts.
Avi Smith1 Department of Diagnostic Sciences, School of Dental Medicine, Tufts University , Boston, Massachusetts.
Anna G Maione2 Department of Cell, Molecular, and Developmental Biology, Sackler School of Graduate Biomedical Sciences, Tufts University , Boston, Massachusetts.
Olga Kashpur1 Department of Diagnostic Sciences, School of Dental Medicine, Tufts University , Boston, Massachusetts.
Gianpaolo Carpinito1 Department of Diagnostic Sciences, School of Dental Medicine, Tufts University , Boston, Massachusetts.
Aristides Veves3 Microcirculation Laboratory and Joslin-Beth Israel Deaconess Foot Center, Beth Israel Deaconess Medical Center, Harvard University , Boston, Massachusetts.
David J Mooney4 Wyss Institute for Biologically Inspired Engineering, School of Engineering and Applied Sciences, Harvard University , Cambridge, Massachusetts.
Jonathan A Garlick1 Department of Diagnostic Sciences, School of Dental Medicine, Tufts University , Boston, Massachusetts.
Tufts University · USBeth Israel Deaconess Medical Center · USInspire Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic foot ulcers (DFUs) are nonhealing chronic wounds that are a serious complication of diabetes. Since induced pluripotent stem cells (iPSCs) may offer a potent source of autologous cells to heal these wounds, we studied if repair-deficient fibroblasts, derived from DFU patients and age- and site-matched control fibroblasts, could be reprogrammed to iPSCs. To establish this, we used Sendai virus to successfully reprogram six primary fibroblast cell lines derived from ulcerated skin of two DFU patients (DFU8, DFU25), nonulcerated foot skin from two diabetic patients (DFF24, DFF9), and healthy foot skin from two nondiabetic patients (NFF12, NFF14). We confirmed reprogramming to a pluripotent state through three independent criteria: immunofluorescent staining for SSEA-4 and TRA-1-81, formation of embryoid bodies with differentiation potential to all three embryonic germ layers in vitro, and formation of teratomas in vivo. All iPSC lines showed normal karyotypes and typical, nonmethylated CpG sites for OCT4 and NANOG. iPSCs derived from DFUs were similar to those derived from site-matched nonulcerated skin from both diabetic and nondiabetic patients. These results have established for the first time that multiple, DFU-derived fibroblast cell lines can be reprogrammed with efficiencies similar to control fibroblasts, thus demonstrating their utility for future regenerative therapy of DFUs.

Indexed as

Cell DifferentiationCellular ReprogrammingAnimalsCells, CulturedDiabetic FootFibroblastsHumansInduced Pluripotent Stem CellsMiceMice, SCIDSendai virusTeratoma

Identifiers

PMID27328415
PMCPMC4964760
OpenAlexW2463282799

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.