TY - JOUR
T1 - What is a β cell? – Chapter I in the Human Islet Research Network (HIRN) review series
AU - Kaestner, Klaus H.
AU - Campbell-Thompson, Martha
AU - Dor, Yuval
AU - Gill, Ronald G.
AU - Glaser, Benjamin
AU - Kim, Seung K.
AU - Sander, Maike
AU - Stabler, Cherie
AU - Stewart, Andrew F.
AU - Powers, Alvin C.
N1 - Publisher Copyright:
© 2021 The Author(s)
PY - 2021/11
Y1 - 2021/11
N2 - Background: The pancreatic β cell, as the sole source of the vital hormone insulin, has been under intensive study for more than a century. Given the potential of newly created insulin-producing cells as a treatment or even cure of type 1 diabetes (T1D) and possibly in severe cases of type 2 diabetes (T2D), multiple academic and commercial laboratories are working to derive surrogate glucose-responsive, insulin-producing cells. Scope of Review: The recent development of advanced phenotyping technologies, including molecular, epigenomic, histological, or functional, have greatly improved our understanding of the critical properties of human β cells. Using this information, here we summarize the salient features of normal, fully functional adult human β cells, and propose minimal criteria for what should rightfully be termed ‘β cells’ as opposed to insulin-producing but not fully-functional surrogates that we propose should be referred to as ‘β-like’ cells or insulin-producing cells. Major Conclusions: Clear criteria can be established to differentiate fully functional, mature β cells from ‘β-like’ surrogates. In addition, we outline important knowledge gaps that must be addressed to enable a greater understanding of the β cell.
AB - Background: The pancreatic β cell, as the sole source of the vital hormone insulin, has been under intensive study for more than a century. Given the potential of newly created insulin-producing cells as a treatment or even cure of type 1 diabetes (T1D) and possibly in severe cases of type 2 diabetes (T2D), multiple academic and commercial laboratories are working to derive surrogate glucose-responsive, insulin-producing cells. Scope of Review: The recent development of advanced phenotyping technologies, including molecular, epigenomic, histological, or functional, have greatly improved our understanding of the critical properties of human β cells. Using this information, here we summarize the salient features of normal, fully functional adult human β cells, and propose minimal criteria for what should rightfully be termed ‘β cells’ as opposed to insulin-producing but not fully-functional surrogates that we propose should be referred to as ‘β-like’ cells or insulin-producing cells. Major Conclusions: Clear criteria can be established to differentiate fully functional, mature β cells from ‘β-like’ surrogates. In addition, we outline important knowledge gaps that must be addressed to enable a greater understanding of the β cell.
KW - Beta cell
KW - Diabetes
KW - Islet
KW - Islet transplantation
UR - http://www.scopus.com/inward/record.url?scp=85116473984&partnerID=8YFLogxK
U2 - 10.1016/j.molmet.2021.101323
DO - 10.1016/j.molmet.2021.101323
M3 - Review article
C2 - 34416394
AN - SCOPUS:85116473984
SN - 2212-8778
VL - 53
JO - Molecular Metabolism
JF - Molecular Metabolism
M1 - 101323
ER -