2169-P: A Gene Expression Network Analysis of the Pancreatic Islets from Lean and Obese Mice Identifies Complement 1q-Like-3 Secreted Protein as a Regulator of Beta-Cell Function

Diabetes ◽  
2019 ◽  
Vol 68 (Supplement 1) ◽  
pp. 2169-P
Author(s):  
JAMES KOLTES ◽  
ITIKA ARORA ◽  
RAJESH GUPTA ◽  
DAN C. NGUYEN ◽  
SUSHANT BHATNAGAR
2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Trine Maxel ◽  
Kamille Smidt ◽  
Charlotte C. Petersen ◽  
Bent Honoré ◽  
Anne K. Christensen ◽  
...  

2007 ◽  
Vol 35 (Database) ◽  
pp. D751-D755 ◽  
Author(s):  
J. M. Mazzarelli ◽  
J. Brestelli ◽  
R. K. Gorski ◽  
J. Liu ◽  
E. Manduchi ◽  
...  

2004 ◽  
Vol 279 (36) ◽  
pp. 37316-37323 ◽  
Author(s):  
Hiroki Takahashi ◽  
Phuong Oanh T. Tran ◽  
Eric LeRoy ◽  
Jamie S. Harmon ◽  
Yoshito Tanaka ◽  
...  

Biology ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 534
Author(s):  
Jamie M. R. Tarlton ◽  
Steven Patterson ◽  
Annette Graham

Alterations in lipid metabolism within beta cells and islets contributes to dysfunction and apoptosis of beta cells, leading to loss of insulin secretion and the onset of type 2 diabetes. Over the last decade, there has been an explosion of interest in understanding the landscape of gene expression which influences beta cell function, including the importance of small non-coding microRNA sequences in this context. This review sought to identify the microRNA sequences regulated by metabolic challenges in beta cells and islets, their targets, highlight their function and assess their possible relevance as biomarkers of disease progression in diabetic individuals. Predictive analysis was used to explore networks of genes targeted by these microRNA sequences, which may offer new therapeutic strategies to protect beta cell function and delay the onset of type 2 diabetes.


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