Preconditioning influences mesenchymal stem cell properties in vitro and in vivo.
Chenxia HuChenxia HuPublished in: Journal of cellular and molecular medicine (2018)
Various diseases and toxic factors easily impair cellular and organic functions in mammals. Organ transplantation is used to rescue organ function, but is limited by scarce resources. Mesenchymal stem cell (MSC)-based therapy carries promising potential in regenerative medicine because of the self-renewal and multilineage potency of MSCs; however, MSCs may lose biological functions after isolation and cultivation for a long time in vitro. Moreover, after they are injected in vivo and migrate into the damaged tissues or organs, they encounter a harsh environment coupled with death signals due to the inadequate tensegrity structure between the cells and matrix. Preconditioning, genetic modification and optimization of MSC culture conditions are key strategies to improve MSC functions in vitro and in vivo, and all of these procedures will contribute to improving MSC transplantation efficacy in tissue engineering and regenerative medicine. Preconditioning with various physical, chemical and biological factors is possible to preserve the stemness of MSCs for further application in studies and clinical tests. In this review, we mainly focus on preconditioning and the corresponding mechanisms for improving MSC activities in vitro and in vivo; we provide a glimpse into the promotion of MSC-based cell therapy development for regenerative medicine. As a promising consequence, MSC transplantation can be applied for the treatment of some terminal diseases and can prolong the survival time of patients in the near future.
Keyphrases
- cell therapy
- mesenchymal stem cells
- umbilical cord
- ischemia reperfusion injury
- stem cells
- tissue engineering
- end stage renal disease
- cerebral ischemia
- bone marrow
- newly diagnosed
- induced apoptosis
- ejection fraction
- mental health
- physical activity
- dna methylation
- peritoneal dialysis
- epithelial mesenchymal transition
- genome wide
- prognostic factors
- risk assessment
- free survival
- patient reported outcomes
- cell proliferation
- cell death
- copy number
- water soluble