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Self-assembly of differentiated dental pulp stem cells facilitates spheroid human dental organoid formation and prevascularization.
Liu, Fei; Xiao, Jing; Chen, Lei-Hui; Pan, Yu-Yue; Tian, Jun-Zhang; Zhang, Zhi-Ren; Bai, Xiao-Chun.
Afiliación
  • Liu F; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, Guangdong Province, China.
  • Xiao J; Department of Health Management, Guangdong Second Provincial General Hospital, Guangzhou 510317, Guangdong Province, China.
  • Chen LH; Guangdong Provincial Key Laboratory of Tumor Interventional Diagnosis and Treatment, Zhuhai People's Hospital Affiliated with Jinan University, Zhuhai 519000, Guangdong Province, China.
  • Pan YY; Centre of Reproduction, Development and Aging, Faculty of Health Sciences, University of Macau, Macau 999078, China.
  • Tian JZ; Department of Stomatology, Guangdong Second Provincial General Hospital, Guangzhou 510317, Guangdong Province, China.
  • Zhang ZR; Department of Stomatology, Guangdong Second Provincial General Hospital, Guangzhou 510317, Guangdong Province, China.
  • Bai XC; Department of Health Management, Guangdong Second Provincial General Hospital, Guangzhou 510317, Guangdong Province, China.
World J Stem Cells ; 16(3): 287-304, 2024 Mar 26.
Article en En | MEDLINE | ID: mdl-38577232
ABSTRACT

BACKGROUND:

The self-assembly of solid organs from stem cells has the potential to greatly expand the applicability of regenerative medicine. Stem cells can self-organise into microsized organ units, partially modelling tissue function and regeneration. Dental pulp organoids have been used to recapitulate the processes of tooth development and related diseases. However, the lack of vasculature limits the utility of dental pulp organoids.

AIM:

To improve survival and aid in recovery after stem cell transplantation, we demonstrated the three-dimensional (3D) self-assembly of adult stem cell-human dental pulp stem cells (hDPSCs) and endothelial cells (ECs) into a novel type of spheroid-shaped dental pulp organoid in vitro under hypoxia and conditioned medium (CM).

METHODS:

During culture, primary hDPSCs were induced to differentiate into ECs by exposing them to a hypoxic environment and CM. The hypoxic pretreated hDPSCs were then mixed with ECs at specific ratios and conditioned in a 3D environment to produce prevascularized dental pulp organoids. The biological characteristics of the organoids were analysed, and the regulatory pathways associated with angiogenesis were studied.

RESULTS:

The combination of these two agents resulted in prevascularized human dental pulp organoids (Vorganoids) that more closely resembled dental pulp tissue in terms of morphology and function. Single-cell RNA sequencing of dental pulp tissue and RNA sequencing of Vorganoids were integrated to analyse key regulatory pathways associated with angiogenesis. The biomarkers forkhead box protein O1 and fibroblast growth factor 2 were identified to be involved in the regulation of Vorganoids.

CONCLUSION:

In this innovative study, we effectively established an in vitro model of Vorganoids and used it to elucidate new mechanisms of angiogenesis during regeneration, facilitating the development of clinical treatment strategies.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: World J Stem Cells Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: World J Stem Cells Año: 2024 Tipo del documento: Article País de afiliación: China