TY - JOUR
T1 - Endoplasmic reticulum stress and pancreatic β-cell death
AU - Fonseca, Sonya G.
AU - Gromada, Jesper
AU - Urano, Fumihiko
N1 - Funding Information:
Work in the laboratory of F. Urano is supported by grants from NIH-NIDDK (R01DK067493), the Diabetes and Endocrinology Research Center at the University of Massachusetts Medical School (5 P30 DK32520), and the Juvenile Diabetes Research Foundation International (1-2008-593 and 40-2011-14). We apologize to those colleagues whose publications could not be cited owing to space limitations.
PY - 2011/7
Y1 - 2011/7
N2 - In pancreatic β-cells, the endoplasmic reticulum (ER) is an important cellular compartment for insulin biosynthesis, which accounts for half of the total protein production in these cells. Protein flux through the ER must be carefully monitored to prevent dysregulation of ER homeostasis and stress. ER stress elicits a signaling cascade known as the unfolded protein response (UPR), which influences both life and death decisions in cells. β-cell loss is a pathological component of both type 1 and type 2 diabetes, and recent findings suggest that ER stress is involved. In this review, we address the transition from the physiological ER stress response to the pathological response, and explore the mechanisms of ER stress-mediated β-cell loss during the progression of diabetes.
AB - In pancreatic β-cells, the endoplasmic reticulum (ER) is an important cellular compartment for insulin biosynthesis, which accounts for half of the total protein production in these cells. Protein flux through the ER must be carefully monitored to prevent dysregulation of ER homeostasis and stress. ER stress elicits a signaling cascade known as the unfolded protein response (UPR), which influences both life and death decisions in cells. β-cell loss is a pathological component of both type 1 and type 2 diabetes, and recent findings suggest that ER stress is involved. In this review, we address the transition from the physiological ER stress response to the pathological response, and explore the mechanisms of ER stress-mediated β-cell loss during the progression of diabetes.
UR - http://www.scopus.com/inward/record.url?scp=79959897450&partnerID=8YFLogxK
U2 - 10.1016/j.tem.2011.02.008
DO - 10.1016/j.tem.2011.02.008
M3 - Review article
C2 - 21458293
AN - SCOPUS:79959897450
SN - 1043-2760
VL - 22
SP - 266
EP - 274
JO - Trends in Endocrinology and Metabolism
JF - Trends in Endocrinology and Metabolism
IS - 7
ER -