Evidence map›Paper›PMID 30832329›Full record

ArticleInternational journal of molecular sciences2019

Pericytes as a Source of Osteogenic Cells in Bone Fracture Healing.

Sopak Supakul, Kenta Yao, Hiroki Ochi, Tomohito Shimada, Kyoko Hashimoto, Satoko Sunamura, Yo Mabuchi, Miwa Tanaka, Chihiro Akazawa, Takuro Nakamura and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Rediscovery of pericytes within the neurovascular unit for cerebral ischemia/reperfusion injury.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Bone marrow adipocytes: key players in vascular niches, aging, and disease.Frontiers in cell and developmental biology · 2025
    Review
  9. Review
  10. Review
  11. Signaling Role of Pericytes in Vascular Health and Tissue Homeostasis.International journal of molecular sciences · 2024
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

13 authors at 3 institutions in 1 country.

Sopak SupakulDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. 140521ms@tmd.ac.jp.
Kenta YaoDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. 130921ms@tmd.ac.jp.
Hiroki OchiDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. ochi.phy2@tmd.ac.jp.ORCID 0000-0002-3960-7710
Tomohito ShimadaDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. 150531ms@tmd.ac.jp.
Kyoko HashimotoDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. 110682ms@tmd.ac.jp.
Satoko SunamuraDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. sunphy2@tmd.ac.jp.
Yo MabuchiDepartment of Biochemistry and Biophysics, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8510, Japan. yomabuchi.bb@tmd.ac.jp.
Miwa TanakaDivision of Carcinogenesis, The Cancer Institute, Japanese Foundation for Cancer Research (JFCR), Tokyo 135-8550, Japan. miwa.tanaka@jfcr.or.jp.
Chihiro AkazawaDepartment of Biochemistry and Biophysics, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8510, Japan. chihiroakazawa@gmail.com.
Takuro NakamuraDivision of Carcinogenesis, The Cancer Institute, Japanese Foundation for Cancer Research (JFCR), Tokyo 135-8550, Japan. nakamurat@jfcr.or.jp.ORCID 0000-0002-0419-7547
Atsushi OkawaDepartment of Orthopaedic Surgery, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. okawa.orth@tmd.ac.jp.
Shu TakedaDivision of Endocrinology, Toranomon Hospital Endocrine Center, Tokyo 105-8470, Japan. takeda.phy2@tmd.ac.jp.
Shingo SatoDepartment of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School, Tokyo 113-8519, Japan. satoshin.phy2@tmd.ac.jp.ORCID 0000-0002-6227-5910
Tokyo Medical and Dental University · JPJapanese Foundation For Cancer Research · JPToranomon Hospital · JP

Funding

Grants-in-Aid for Scientific Research (KAKENHI) #16K10847the Core Research for Evolutional Science and Technology (AMED-CREST) #JP18gm0610008
6 · The paper itself

Abstract

Pericytes are mesenchymal cells that surround the endothelial cells of small vessels in various organs. These cells express several markers, such as NG2, CD146, and PDGFRβ, and play an important role in the stabilization and maturation of blood vessels. It was also recently revealed that like mesenchymal stem cells (MSCs), pericytes possess multilineage differentiation capacity, especially myogenic, adipogenic, and fibrogenic differentiation capacities. Although some previous studies have reported that pericytes also have osteogenic potential, the osteogenesis of pericytes can still be further elucidated. In the present study, we established novel methods for isolating and culturing primary murine pericytes. An immortalized pericyte line was also established. Multilineage induction of the pericyte line induced osteogenesis, adipogenesis, and chondrogenesis of the cells in vitro. In addition, pericytes that were injected into the fracture site of a bone fracture mouse model contributed to callus formation. Furthermore, in vivo pericyte-lineage-tracing studies demonstrated that endogenous pericytes also differentiate into osteoblasts and osteocytes and contribute to bone fracture healing as a cellular source of osteogenic cells. Pericytes can be a promising therapeutic candidate for treating bone fractures with a delayed union or nonunion as well as bone diseases causing bone defects.

Indexed as

ChondrogenesisFracture HealingOsteogenesisAnimalsCell DifferentiationCell LineCells, CulturedChondrocytesMesenchymal Stem Cell TransplantationMiceMice, Inbred BALB COsteoblastsPericytesPrimary Cell Culturebone fracture healingosteogenic differentiationpericyte

Identifiers

PMID30832329
PMCPMC6429337
OpenAlexW2919113234

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.