Clinical applicability of optogenetic gene regulation. Issue 11 (29th July 2021)

• Record Type: Journal Article
• Authors: Wichert, Nina; Witt, Martin; Blume, Cornelia; Scheper, Thomas
• Is Part Of: Biotechnology and bioengineering. Volume 118:Issue 11(2021)
• Page Start: 4168
• Page End: 4185
• Publication Date: 2021-07-29
• Subjects: clinical applications -- gene and protein regulation -- mammalian cells -- optogenetics; Biotechnology -- Periodicals; Bioengineering -- Periodicals; 660.6
• DOI: 10.1002/bit.27895
• Languages: English
• ISSNs: 0006-3592

Abstract

Abstract: The field of optogenetics is rapidly growing in relevance and number of developed tools. Among other things, the optogenetic repertoire includes light‐responsive ion channels and methods for gene regulation. This review will be confined to the optogenetic control of gene expression in mammalian cells as suitable models for clinical applications. Here optogenetic gene regulation might offer an excellent method for spatially and timely regulated gene and protein expression in cell therapeutic approaches. Well‐known systems for gene regulation, such as the LOV‐, CRY2/CIB‐, PhyB/PIF‐systems, as well as other, in mammalian cells not yet fully established systems, will be described. Advantages and disadvantages with regard to clinical applications are outlined in detail. Among the many unanswered questions concerning the application of optogenetics, we discuss items such as the use of exogenous chromophores and their effects on the biology of the cells and methods for a gentle, but effective gene transfection method for optogenetic tools for in vivo applications. Abstract : The field of optogenetics is rapidly growing since the use of optogenetic tools evokes the hope that cell‐specific protein expression will be spatially and timely regulable by light. Here, we focus on the optogenetic control of gene and protein expression in mammalian cells as suitable models for clinical applications. Well‐known systems for gene regulation, such as LOV‐, CRY2/CIB‐, and PhyB/PIF‐systems will be described and their advantages and disadvantages discussed, although not all of them are successfully established in human cells.