間葉系幹細胞/間質細胞株 (ASCL) を用いた新しい肝臓再生法の開発

Material type: 文書・図像類

Author: 尾原, 秀明

Publisher: 慶應義塾大学

Publication date: 2020

Material Format: Digital

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Note (General)：: type:text背景/目的：本研究では、in vitro肝虚血再灌流障害モデルにおける間葉系幹細胞/間質細胞株(Adipose stem/stromal cell line, ASCL)の細胞増殖・再生・修復機能を検証する。方法として、Wister系ラットの肝細胞をASCLとともに共培養し、低酸素...

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Material Type: 文書・図像類
Title: 間葉系幹細胞/間質細胞株 (ASCL) を用いた新しい肝臓再生法の開発
Author/Editor: 尾原, 秀明
Author Heading: 尾原, 秀明
Publication, Distribution, etc.: 慶應義塾大学
Publication Date: 2020
Publication Date (W3CDTF): 2020
Alternative Title: カンヨウケイカンサイボウ/カンシツサイボウカブ (ASCL) オモチイタアタラシイカンゾウサイセイホウノカイハツ
Kan'yōkei kansaibō/kanshitsu saibōkabu (ASCL) o mochiita atarashii kanzō saiseihō no kaihatsu
Therapeutic potential of adipose tissue-derived stem cell lines in liver regeneration
Periodical title: 学事振興資金研究成果実績報告書
Text Language Code: jpn
eng
Target Audience: 一般
Note (General): type:text
背景/目的：本研究では、in vitro肝虚血再灌流障害モデルにおける間葉系幹細胞/間質細胞株(Adipose stem/stromal cell line, ASCL)の細胞増殖・再生・修復機能を検証する。方法として、Wister系ラットの肝細胞をASCLとともに共培養し、低酸素培養による細胞障害および細胞生存率をLDH測定およびTUNEL法により評価を行う。また、低酸素障害後の細胞を回収しAlb、IL-6、IL-1α、HMGB-1、NF-κB、ERK1/2、HGF、SODの遺伝子及びタンパク発現を測定する。結果：ヒトASCLの技術を応用し、ラット皮下脂肪組織より間葉系幹細胞(Adipose stem cell, ASC)を単離し成熟脂肪細胞へ分化させ、再び脱分化を誘導しASCLの樹立に成功した。ASCLの治療効果を検討するため、肝虚血再灌流モデルラットにそれぞれ生理食塩水、ASC、ASCLを脾臓に投与し3群に分けて比較検討した。結果は、ASCL投与群のラットは生理食塩水とASC群と比較して、AST・ALTの上昇が抑制されていた。肝臓の免疫組織化学染色による病理組織学的検討では、生理食塩水群のラットと比べ、ASC群とASCL群において活性化Caspase-1の発現量が著明に抑制されていた。肝細胞低酸素障害実験では、単離したラット肝細胞をASCもしくはASCLとそれぞれと共培養し、単独培養群と共に1%酸素濃度で3時間の低酸素ストレスを加えた。低酸素障害後、TUNEL染色法によりアポトーシスの評価を行った結果、ASC及びASCL共培養群におけるTUNEL発現量は単独培養群に比べ有意に低発現であった。培養上清中のLDHを測定した結果、同様にASC及びASCL共培養群において有意に低値であり細胞障害が抑制されることが示唆された。また、遺伝子発現解析では単独培養群に比べASC及びASCL共培養群において抗炎症作用を有するTGF-β、IL-10、IL-1RAのmRNA発現の増加が確認された。以上の結果より、ASC及びASCLは肝臓虚血再灌流損害を抑制する働きを有することが示唆された。 In this study, we purpose to find out evidence of adipose stem/stromal cell line (ASCL) suppressing the apoptosis process in in-vitro liver ischemia/reperfusion injury model. We also aim to verify ASCLs can attenuate liver ischemia/reperfusion injury by promoting cell proliferation, regeneration and repair function. Hepatocytes are isolated from liver tissue of Wistar rats and co-cultured with ASCLs as a method. By incubating in hypoxia environment, co-culture groups are induced to cell damage. The hypoxia injury is assessed by cell viability and apoptosis progression respectively with LDH and TUNEL measurement. To analyze more details in mechanism of ASCLs cell therapy in liver injury, co-cultured cells are collected after hypoxia for assessing gene and protein level expression such as ALB, IL-6, IL-1α, HMGB-1, NF-κB, ERK1/2, HGF, SOD. The procedure of establishing rat-derived ASCLs was referred to the protocol of human-derived ASCLs' establishment. Briefly, adipose stem cells (ASC) were extracted from Wistar rats' lateral abdominal fat and induced its differentiation so that extracted ASCs were differentiated into mature adipocytes. ASCLs were produced by de-differentiation of mature adipocytes eventually. To assess therapeutic potential of ASCLs, rats induced to hepatic ischemia/reperfusion were divided into control, ASC and ASCL injecting groups and injected with normal saline, ASCs and ASCLs respectively. As a result, increases in serum concentrations of AST and ALT in ASCL group were significantly suppressed comparing to ones in the control and ASC group. To observe the pathological changes in liver tissue, immunohistology staining was analyzed in each group of individuals. Activated Caspase-1 was highly expressed in control group's liver tissue while suppressed in ASC and ASCL's one. In hepatocytes' hypoxia/reoxygenation experiment, isolated hepatocytes were co-cultured with ASCs or ASCLs respectively, these co-culture groups and single culture of hepatocytes as control group were incubated in the environment of 1% O2 and 5% CO2 for 3 hours so as to add hypoxia stress. TUNEL staining was used for assessing apoptosis progression after hypoxia injury. As a result, TUNEL expression was significantly low expressed in ASC and ASCL co-culture group. Similar result was showed in LDH level of each group's culture medium which suggest both ASCs and ASCLs are able to alleviate cell damage. In gene expression analyze, mRNA expressions of anti-inflammatory cytokines such as TGF-β, IL-10, IL-1RA were increased in ASC and ASCL co-culture group comparing to control group. In conclusion, both ASCs and ASCLs have ability to suppress injury from hepatic ischemia/reperfusion according to current results.
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Original Data Provider (Database): 慶應義塾大学 : 慶應義塾大学学術情報リポジトリ