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Effect of Histone Deacetylase Inhibitors on Differentiation of Human Bone Marrow-derived Stem Cells Into Neuron-like Cells

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  • 발행기관
    조선대학교 기초과학연구원 바로가기
  • 간행물
    통합자연과학논문집(구 조선자연과학논문집) KCI 등재 바로가기
  • 통권
    제12권 4호 (2019.12)바로가기
  • 페이지
    pp.133-141
  • 저자
    Sujeong Jang, Seokho Park, Hyong-Ho Cho, Ung Yang, Maru Kang, Jong-Seong Park, Sah-Hoon Park, Han-Seong Jeong
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A368478

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원문정보

초록

영어
Mesenchymal stem cells (MSCs) are known to differentiate into multiple lineages, making neurogenic differentiation an important target in the clinical field. In the present study, we induced the neurogenic differentiation of cells using histone deacetylase (HDAC) inhibitors and studied their mechanisms for further differentiation in vitro. We treated cells with the HDAC inhibitors, MS-275 and NaB; and found that the cells had neuron-like features such as distinct bipolar or multipolar morphologies with branched processes. The mRNA expressions encoding for NEFL, MAP2, TUJ1, OLIG2, and SYT was significantly increased following HDAC inhibitors treatment compared to without HDAC inhibitors; high protein levels of MAP2 and Tuj1 were detected by immunofluorescence staining. We examined the mechanisms of differentiation and found that the Wnt signaling pathway and downstream mitogen-activate protein kinase were involved in neurogenic differentiation of MSCs. Importantly, Wnt4, Wnt5a/b, and Wnt11 protein levels were highly increased after treatment with NaB; signals were activated through the regulation of Dvl2 and Dvl3. Interestingly, NaB treatment increased the levels of JNK and upregulated JNK phosphorylation. After MS-275 treatment, Wnt protein levels were decreased and GSK-3β was phosphorylated. In this cell, HDAC inhibitors controlled the non-canonical Wnt expression by activating JNK phosphorylation and the canonical Wnt signaling by targeting GSK-3β.

목차

Abstract
1. Introduction
2. Methods
2.1. Cell lines and reagents
2.2. Immunocytochemistry
2.3. Reverse Transcriptase-polymerase Chain Reaction (RT-PCR) Analysis
2.4. Quantitative RT-PCR
2.5. Western Blot Assay
2.6. Statistics
3. Results
3.1. HDAC Inhibitors Enhance Neuron-like Cell Differentiation of hBM-MSCs in Vitro
3.2. HDAC Inhibitors Regulate Wnt Pathway and Downstream JNK Signaling
4. Discussion
5. Conclusions
Acknowledgments
References

키워드

Glycogen Synthase Kinase 3 Histone Deacetylase Inhibitors Mesenchymal Stromal Cells Wnt Signaling Pathway Cell Differentiation

저자

  • Sujeong Jang [ Department of Physiology, Chonnam National University Medical School, Jellanamdo 58128, Korea ]
  • Seokho Park [ Department of Physiology, Chonnam National University Medical School, Jellanamdo 58128, Korea ]
  • Hyong-Ho Cho [ Department of Otolaryngology-Head and Neck Surgery, Chonnam National University Medical School, Gwangju 61469, Korea ]
  • Ung Yang [ Department of Horticulture, Asian Pear Research Institute, College of Agriculture and Life Sciences, Chonnam National University, Gwangju 61186, Korea ]
  • Maru Kang [ Department of Defense Science & Technology, Gwangju University, Gwangju 61743, Korea ]
  • Jong-Seong Park [ Department of Physiology, Chonnam National University Medical School, Jellanamdo 58128, Korea ]
  • Sah-Hoon Park [ Department of Physiology, Chonnam National University Medical School, Jellanamdo 58128, Korea ]
  • Han-Seong Jeong [ Department of Physiology, Chonnam National University Medical School, Jellanamdo 58128, Korea ] Corresponding author

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    조선대학교 기초과학연구원 [The Natural Science Research Institute of Chosun]
  • 설립연도
    2008
  • 분야
    자연과학>자연과학일반
  • 소개
    본 연구원은 기초과학을 진흥하기 위한 연구·교육 및 그 보급을 목적으로 한다. 이 목적을 달성하기 위하여 다음 각 호의 사업을 수행한다. 1. 기초과학 제 분야에 관한 조사와 연구 2. 기초과학에 관한 학술행사(학술대회, 학술세미나, 심포지엄, 초청강연회 등) 개최 3. 학문후속세대 및 일반인을 위한 기초과학 교육 4. 기관지『조선자연과학논문지』 발간 5. 『자연과학연구총서』, 『자연과학번역총서』 등 단행본 발간 6. 기타 본 연구원의 목적과 관련된 사업

간행물

  • 간행물명
    통합자연과학논문집(구 조선자연과학논문집) [Journal of Integrative Natural Science]
  • 간기
    계간
  • pISSN
    2005-1042
  • 수록기간
    2008~2025
  • 등재여부
    KCI 등재
  • 십진분류
    KDC 405 DDC 505

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