TY - CHAP
T1 - Cell Surface Enzymatic Engineering-Based Approaches to Improve Cellular Therapies
AU - AbuElela, Ayman
AU - Sakashita, Kosuke
AU - Merzaban, Jasmeen
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2014/6/7
Y1 - 2014/6/7
N2 - The cell surface represents the interface between the cell and its environment. As such, the cell surface controls cell–cell interactions and functions such as adhesion and migration, and will transfer external cues to regulate processes such as survival, death, and differentiation. Redefining the cell surface by temporarily (or permanently) modifying the molecular landscape of the plasma membrane affects the way in which the cell interacts with its environment and influences the information that is relayed into the cell along downstream signaling pathways. This chapter outlines the role of key enzymes, the glycosyltransferases, in posttranslationally modifying proteins and lipids to fine-tune cells, ability to migrate. These enzymes are critical in controlling the formation of a platform structure, sialyl Lewis x (sLex), on circulating cells that plays a central role in the recognition and recruitment by selectin counter receptors on endothelial cells that line blood vessels of tissues throughout the body. By developing methods to manipulate the activity of these enzymes and hence the cell surface structures that result, treatments can be envisioned that direct the migration of therapeutic cells to specific locations throughout the body and also to inhibit metastasis of detrimental cells such as circulating tumor cells.
AB - The cell surface represents the interface between the cell and its environment. As such, the cell surface controls cell–cell interactions and functions such as adhesion and migration, and will transfer external cues to regulate processes such as survival, death, and differentiation. Redefining the cell surface by temporarily (or permanently) modifying the molecular landscape of the plasma membrane affects the way in which the cell interacts with its environment and influences the information that is relayed into the cell along downstream signaling pathways. This chapter outlines the role of key enzymes, the glycosyltransferases, in posttranslationally modifying proteins and lipids to fine-tune cells, ability to migrate. These enzymes are critical in controlling the formation of a platform structure, sialyl Lewis x (sLex), on circulating cells that plays a central role in the recognition and recruitment by selectin counter receptors on endothelial cells that line blood vessels of tissues throughout the body. By developing methods to manipulate the activity of these enzymes and hence the cell surface structures that result, treatments can be envisioned that direct the migration of therapeutic cells to specific locations throughout the body and also to inhibit metastasis of detrimental cells such as circulating tumor cells.
UR - http://hdl.handle.net/10754/608652
UR - http://www.sciencedirect.com/science/article/pii/B978145573146600009X
UR - http://www.scopus.com/inward/record.url?scp=84941799961&partnerID=8YFLogxK
U2 - 10.1016/B978-1-4557-3146-6.00009-X
DO - 10.1016/B978-1-4557-3146-6.00009-X
M3 - Chapter
SN - 978-1-4557-3146-6
SP - 175
EP - 213
BT - Micro- and Nanoengineering of the Cell Surface
PB - Elsevier BV
ER -