p14: therapeutic potential of induced pluripotent stem cells for spinal cord injury

Authors

sara abdolahi a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran b. department of biotechnology, school of veterinary science, shiraz university, shiraz, iran

maryam borhani-haghighi a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran b. department of anatomy, tehran university of medical sciences, tehran, iran

hadi aligholi a. shefa neuroscience research center, khatam alanbia hospital, tehran, iran b. department of neuroscience, school of advanced medical sciences and technologies, shiraz university of medical sciences, shiraz, iran

abstract

spinal cord injury (sci) is a destructive event that often lead to permanent neurologic deficit. current clinical treatments are aimed at preventing secondary damage, promoting regeneration, and replacing destroyed spinal cord tissue, although effective treatments for sci remain limited. cell therapies for treating sci are promising therapy for replacing dead cells, neuroprotection and axon regeneration. a number of different pluripotent, multipotent, and differentiating stem cells have been investigated so far for the treatment of sci. some of these cells have entered or will soon be entering clinical trials. basic and pre-clinical experimental studies have highlighted the positive effects of induced pluripotent stem cells (ipscs) treatment after spinal cord and peripheral nerve injury. ipscs are a type of pluripotent stem cell that directly can be generated from adult cells and their therapeutic effects are believed to be due to their potential to differentiate into neural precursor cells, neurons, oligodendrocytes, astrocytes  and neural crest cells that can act by replacing lost cells or providing environmental support. ipscs can provide a cell source that has characteristics of embryonic stem cells. however, human ipscs solve the ethical dilemma posed by human embryonic stem cells research. in addition, they can be sourced from autologous sources, which may decrease the risk of immune rejection.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

P46: Therapeutic Potential of Neural Stem Cells for Spinal Cord Injury

لطفاً به چکیده انگلیسی مراجعه شود.

full text

P47: Application of Induced Pluripotent Stem Cells in Spinal Cord Injury Treatment

لطفاً به چکیده انگلیسی مراجعه شود.

full text

[Therapeutic potential of induced pluripotent stem cells for spinal cord injury].

Once the safety issue has been overcome, induced pluripotent stem cells (iPSCs), which do not entail ethical or immunological concerns, may become the preferred cell source for regenerative medicine. Various types of iPSCs have been established by different methods, and each type exhibits different biological properties. Before iPSC-based clinical applications can be initiated, detailed evaluat...

full text

Therapeutic potential of appropriately evaluated safe-induced pluripotent stem cells for spinal cord injury.

Various types of induced pluripotent stem (iPS) cells have been established by different methods, and each type exhibits different biological properties. Before iPS cell-based clinical applications can be initiated, detailed evaluations of the cells, including their differentiation potentials and tumorigenic activities in different contexts, should be investigated to establish their safety and ...

full text

Induced Pluripotent Stem Cells for Traumatic Spinal Cord Injury

Spinal cord injury (SCI) is a common cause of mortality and neurological morbidity. Although progress had been made in the last decades in medical, surgical, and rehabilitation treatments for SCI, the outcomes of these approaches are not yet ideal. The use of cell transplantation as a therapeutic strategy for the treatment of SCI is very promising. Cell therapies for the treatment of SCI are li...

full text

My Resources

Save resource for easier access later


Journal title:
مجله علوم اعصاب شفای خاتم

جلد ۳، شماره ۴، صفحات ۴۱-۴۱

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023