Evidence map›Paper›PMID 33707490›Full record

ArticleScientific reports2021

A novel role for bone marrow-derived cells to recover damaged keratinocytes from radiation-induced injury.

Junko Okano, Yuki Nakae, Takahiko Nakagawa, Miwako Katagi, Tomoya Terashima, Daisuke Nagakubo, Takashi Nakayama, Osamu Yoshie, Yoshihisa Suzuki, Hideto Kojima

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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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

10 authors at 4 institutions in 1 country.

Junko OkanoDepartment of Plastic and Reconstructive Surgery, Shiga University of Medical Science, Shiga, Japan. jokano@belle.shiga-med.ac.jp.
Yuki NakaeDepartment of Stem Cell Biology and Regenerative Medicine, Shiga University of Medical Science, Shiga, Japan.
Takahiko NakagawaDepartment of Nephrology, Otowa Hospital, Kyoto, Japan.
Miwako KatagiDepartment of Stem Cell Biology and Regenerative Medicine, Shiga University of Medical Science, Shiga, Japan.
Tomoya TerashimaDepartment of Stem Cell Biology and Regenerative Medicine, Shiga University of Medical Science, Shiga, Japan.
Daisuke NagakuboFaculty of Pharmaceutical Sciences, Division of Health and Hygienic Sciences, Himeji Dokkyo University, Hyogo, Japan.
Takashi NakayamaDivision of Chemotherapy, Faculty of Pharmacy, Kindai University, Osaka, Japan.
Osamu YoshieThe Health and Kampo Institute, Miyagi, Japan.
Yoshihisa SuzukiDepartment of Plastic and Reconstructive Surgery, Shiga University of Medical Science, Shiga, Japan.
Hideto KojimaDepartment of Stem Cell Biology and Regenerative Medicine, Shiga University of Medical Science, Shiga, Japan.
Shiga University of Medical Science · JPHimeji Dokkyo University · JPKindai University · JPRakuwakai Otowa Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exposure to moderate doses of ionizing radiation (IR), which is sufficient for causing skin injury, can occur during radiation therapy as well as in radiation accidents. Radiation-induced skin injury occasionally recovers, although its underlying mechanism remains unclear. Moderate-dose IR is frequently utilized for bone marrow transplantation in mice; therefore, this mouse model can help understand the mechanism. We had previously reported that bone marrow-derived cells (BMDCs) migrate to the epidermis-dermis junction in response to IR, although their role remains unknown. Here, we investigated the role of BMDCs in radiation-induced skin injury in BMT mice and observed that BMDCs contributed to skin recovery after IR-induced barrier dysfunction. One of the important mechanisms involved the action of CCL17 secreted by BMDCs on irradiated basal cells, leading to accelerated proliferation and recovery of apoptosis caused by IR. Our findings suggest that BMDCs are key players in IR-induced skin injury recovery.

Indexed as

AnimalsBone Marrow CellsBone Marrow TransplantationCell MovementCell ProliferationChemokine CCL17DermisEpidermisGene DeletionHaCaT CellsHumansKeratinocytesMacrophagesMiceMice, Inbred C57BLMice, TransgenicChemokine CCL17Receptors, CCR4

Identifiers

PMID33707490
PMCPMC7952382
OpenAlexW3134912620

What OpenQuestion holds

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Registered trials

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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.