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Computational Strategies for Niche-Dependent Cell Conversion to Assist Stem Cell Therapy
The field of regenerative medicine has blossomed in recent decades. However, the ultimate goal of tissue regeneration – replacing damaged or aged cells with healthy functioning cells – still faces a number of challenges. In particular, better understanding of the role of the cellular niche in shapin...
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Published in: | Trends in biotechnology (Regular ed.) 2019-07, Vol.37 (7), p.687-696 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The field of regenerative medicine has blossomed in recent decades. However, the ultimate goal of tissue regeneration – replacing damaged or aged cells with healthy functioning cells – still faces a number of challenges. In particular, better understanding of the role of the cellular niche in shaping stem cell phenotype and conversion would aid in improving current protocols for stem cell therapies. In this regard, the implementation of novel computational approaches that consider the niche effect on stem cells would be valuable. Here we discuss current problems in stem cell transplantation and rejuvenation, and we propose computational strategies to control niche-dependent cell conversion to overcome them.
Cellular niche shapes stem cell phenotype and conditions cell conversion. Therefore, stem cell conversion should be considered a niche-specific process.
Current computational methods for cell conversion do not consider the niche effect and therefore are not able to predict niche-dependent cell conversion factors.
Single-cell RNA-seq allows the gene expression profiling of cell subpopulations in a given niche and therefore enables the modeling of niche-specific cell conversion.
We propose a computational strategy for the development of single-cell-based methods for niche-dependent cell conversion and its application to stem cell transplantation and rejuvenation. |
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ISSN: | 0167-7799 1879-3096 |
DOI: | 10.1016/j.tibtech.2019.01.005 |