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2018 Fiscal Year Final Research Report

Mesenchymal stem cell therapy for pulmonary fibrosis in new mouse model of pulmonary fibrosis

Research Project

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Project/Area Number 16K19463
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Respiratory organ internal medicine
Research InstitutionNara Medical University

Principal Investigator

Kumamoto Makiko  奈良県立医科大学, 医学部, 助教 (10623522)

Project Period (FY) 2016-04-01 – 2019-03-31
Keywords肺線維症 / 脂肪由来間葉系幹細胞 / 新規肺線維症マウスモデル
Outline of Final Research Achievements

Adipose-derived mesenchymal stem cells(ASC) ameliorate bleomycin-induced pulmonary fibrosis in mice.In addition, ASCs were also effective in new pulomnary fibrosis model in mice. In this new model, pulmonary fibrosis was initiated by the intravenous introduction of primary human fibroblast lines into immunodeficient mice.
The decrease of the expression of fibrotic markers in fibroblasts derived from IPF patient's lung was detected by co-culture with ASC.
Hepatocyte growth factor(HGF) produced from ASC is important for this effect.

Free Research Field

呼吸器内科学

Academic Significance and Societal Importance of the Research Achievements

特発性肺線維症(IPF)には未だ有効な治療手段がなく、新規治療法の開発は急務である。筆者らはブレオマイシン(BLM)肺線維症モデルにおいて骨髄由来間葉系幹細胞の有効性はすでに報告しているが、今回、骨髄由来に比べて低侵襲で確保が容易な脂肪由来間葉系幹細胞(ASC)の線維化抑制効果について証明した。また、IPF患者由来の線維芽細胞を移入することで作成される、よりIPFの病態に近い新規肺線維症マウスモデルにおいても、ASCの効果を証明した。これらの結果は、IPFに対する間葉系幹細胞の臨床応用に向けて、さらに前進させたと考える。

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Published: 2020-03-30  

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