TY - JOUR
T1 - Perilipin 2 downregulation in β cells impairs insulin secretion under nutritional stress and damages mitochondria
AU - Mishra, Akansha
AU - Liu, Siming
AU - Promes, Joseph
AU - Harata, Mikako
AU - Sivitz, William
AU - Fink, Brian
AU - Bhardwaj, Gourav
AU - O’Neill, Brian T.
AU - Kang, Chen
AU - Sah, Rajan
AU - Strack, Stefan
AU - Stephens, Samuel
AU - King, Timothy
AU - Jackson, Laura
AU - Greenberg, Andrew S.
AU - Anokye-Danso, Frederick
AU - Ahima, Rexford S.
AU - Ankrum, James
AU - Imai, Yumi
N1 - Publisher Copyright:
© 2021, Mishra et al.
PY - 2021/5/10
Y1 - 2021/5/10
N2 - Perilipin 2 (PLIN2) is a lipid droplet (LD) protein in β cells that increases under nutritional stress. Downregulation of PLIN2 is often sufficient to reduce LD accumulation. To determine whether PLIN2 positively or negatively affects β cell function under nutritional stress, PLIN2 was downregulated in mouse β cells, INS1 cells, and human islet cells. β Cell–specific deletion of PLIN2 in mice on a high-fat diet reduced glucose-stimulated insulin secretion (GSIS) in vivo and in vitro. Downregulation of PLIN2 in INS1 cells blunted GSIS after 24-hour incubation with 0.2 mM palmitic acid. Downregulation of PLIN2 in human pseudoislets cultured at 5.6 mM glucose impaired both phases of GSIS, indicating that PLIN2 is critical for GSIS. Downregulation of PLIN2 decreased specific OXPHOS proteins in all 3 models and reduced oxygen consumption rates in INS1 cells and mouse islets. Moreover, we found that PLIN2-deficient INS1 cells increased the distribution of a fluorescent oleic acid analog to mitochondria and showed signs of mitochondrial stress, as indicated by susceptibility to fragmentation and alterations of acyl-carnitines and glucose metabolites. Collectively, PLIN2 in β cells has an important role in preserving insulin secretion, β cell metabolism, and mitochondrial function under nutritional stress.
AB - Perilipin 2 (PLIN2) is a lipid droplet (LD) protein in β cells that increases under nutritional stress. Downregulation of PLIN2 is often sufficient to reduce LD accumulation. To determine whether PLIN2 positively or negatively affects β cell function under nutritional stress, PLIN2 was downregulated in mouse β cells, INS1 cells, and human islet cells. β Cell–specific deletion of PLIN2 in mice on a high-fat diet reduced glucose-stimulated insulin secretion (GSIS) in vivo and in vitro. Downregulation of PLIN2 in INS1 cells blunted GSIS after 24-hour incubation with 0.2 mM palmitic acid. Downregulation of PLIN2 in human pseudoislets cultured at 5.6 mM glucose impaired both phases of GSIS, indicating that PLIN2 is critical for GSIS. Downregulation of PLIN2 decreased specific OXPHOS proteins in all 3 models and reduced oxygen consumption rates in INS1 cells and mouse islets. Moreover, we found that PLIN2-deficient INS1 cells increased the distribution of a fluorescent oleic acid analog to mitochondria and showed signs of mitochondrial stress, as indicated by susceptibility to fragmentation and alterations of acyl-carnitines and glucose metabolites. Collectively, PLIN2 in β cells has an important role in preserving insulin secretion, β cell metabolism, and mitochondrial function under nutritional stress.
UR - http://www.scopus.com/inward/record.url?scp=85106215081&partnerID=8YFLogxK
U2 - 10.1172/jci.insight.144341
DO - 10.1172/jci.insight.144341
M3 - Article
C2 - 33784258
AN - SCOPUS:85106215081
SN - 2379-3708
VL - 6
JO - JCI Insight
JF - JCI Insight
IS - 9
M1 - e144341
ER -