Evidence map›Paper›PMID 27388242›Full record

ArticleStem cells translational medicine2016

Perivascular Progenitor Cells Derived From Human Embryonic Stem Cells Exhibit Functional Characteristics of Pericytes and Improve the Retinal Vasculature in a Rodent Model of Diabetic Retinopathy.

Jung Mo Kim, Ki-Sung Hong, Won Kyung Song, Daekyeong Bae, In-Kyu Hwang, Jong Soo Kim, Hyung-Min Chung

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

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  19. Bone Marrow CD133Cell transplantation · 2018
    Article
  20. Vascular stem/progenitor cells: functions and signaling pathways.Cellular and molecular life sciences : CMLS · 2018
    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

7 authors at 2 institutions in 2 countries.

Jung Mo KimDepartment of Tissue Morphogenesis, Max-Planck Institute for Molecular Biomedicine, Münster, Germany.
Ki-Sung HongStem Cell Research Lab, Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, Republic of Korea.
Won Kyung SongDepartment of Ophthalmology, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea.
Daekyeong BaeStem Cell Research Lab, Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, Republic of Korea.
In-Kyu HwangStem Cell Research Lab, Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, Republic of Korea.
Jong Soo KimStem Cell Research Lab, Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, Republic of Korea.
Hyung-Min ChungStem Cell Research Lab, Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, Republic of Korea hmchung@kku.ac.kr.
Konkuk University · KRCHA University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelled: Diabetic retinopathy (DR) is the leading cause of blindness in working-age people. Pericyte loss is one of the pathologic cellular events in DR, which weakens the retinal microvessels. Damage to the microvascular networks is irreversible and permanent; thus further progression of DR is inevitable. In this study, we hypothesize that multipotent perivascular progenitor cells derived from human embryonic stem cells (hESC-PVPCs) improve the damaged retinal vasculature in the streptozotocin-induced diabetic rodent models. We describe a highly efficient and feasible protocol to derive such cells with a natural selection method without cell-sorting processes. As a cellular model of pericytes, hESC-PVPCs exhibited marker expressions such as CD140B, CD146, NG2, and functional characteristics of pericytes. Following a single intravitreal injection into diabetic Brown Norway rats, we demonstrate that the cells localized alongside typical perivascular regions of the retinal vasculature and stabilized the blood-retinal barrier breakdown. Findings in this study highlight a therapeutic potential of hESC-PVPCs in DR by mimicking the role of pericytes in vascular stabilization. SIGNIFICANCE: This study provides a simple and feasible method to generate perivascular progenitor cells from human embryonic stem cells. These cells share functional characteristics with pericytes, which are irreversibly lost at the onset of diabetic retinopathy. Animal studies demonstrated that replenishing the damaged pericytes with perivascular progenitor cells could restore retinal vascular integrity and prevent fluid leakage. This provides promising and compelling evidence that perivascular progenitor cells can be used as a novel therapeutic agent to treat diabetic retinopathy patients.

Indexed as

AnimalsCell Culture TechniquesCell DifferentiationDiabetes Mellitus, ExperimentalDiabetic RetinopathyDisease Models, AnimalHuman Embryonic Stem CellsHumansMultipotent Stem CellsOligonucleotide Array Sequence AnalysisPericytesRatsBlood-retinal barrierDiabetic retinopathyHuman embryonic stem cellsPericytesPerivascular progenitor cells

Identifiers

PMID27388242
PMCPMC4996442
OpenAlexW2461708130

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.