Your browser doesn't support javascript.
loading
In Vivo Reprogramming Using Yamanaka Factors in the CNS: A Scoping Review.
Cho, Han Eol; Lee, Siwoo; Seo, Jung Hwa; Kang, Seong-Woong; Choi, Won Ah; Cho, Sung-Rae.
Afiliación
  • Cho HE; Rehabilitation Institute of Neuromuscular Disease, Yonsei University College of Medicine, Seoul 06229, Republic of Korea.
  • Lee S; Department of Rehabilitation Medicine, Gangnam Severance Hospital, Seoul 06229, Republic of Korea.
  • Seo JH; Graduate Program of Biomedical Engineering, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Kang SW; Department of Rehabilitation Medicine, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Choi WA; Department of Rehabilitation Medicine, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
  • Cho SR; Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Cells ; 13(4)2024 Feb 15.
Article en En | MEDLINE | ID: mdl-38391956
ABSTRACT
Central nervous system diseases, particularly neurodegenerative disorders, pose significant challenges in medicine. These conditions, characterized by progressive neuronal loss, have remained largely incurable, exacting a heavy toll on individuals and society. In recent years, in vivo reprogramming using Yamanaka factors has emerged as a promising approach for central nervous system regeneration. This technique involves introducing transcription factors, such as Oct4, Sox2, Klf4, and c-Myc, into adult cells to induce their conversion into neurons. This review summarizes the current state of in vivo reprogramming research in the central nervous system, focusing on the use of Yamanaka factors. In vivo reprogramming using Yamanaka factors has shown promising results in several animal models of central nervous system diseases. Studies have demonstrated that this approach can promote the generation of new neurons, improve functional outcomes, and reduce scar formation. However, there are still several challenges that need to be addressed before this approach can be translated into clinical practice. These challenges include optimizing the efficiency of reprogramming, understanding the cell of origin for each transcription factor, and developing methods for reprogramming in non-subventricular zone areas. Further research is needed to overcome the remaining challenges, but this approach has the potential to revolutionize the way we treat central nervous system disorders.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Central / Reprogramación Celular Límite: Animals / Humans Idioma: En Revista: Cells Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Central / Reprogramación Celular Límite: Animals / Humans Idioma: En Revista: Cells Año: 2024 Tipo del documento: Article