Metabolic Stress Impairs Pericyte Response to Optogenetic Stimulation in Pancreatic Islets

被引:5
作者
Michau, Aurelien [1 ]
Lafont, Chrystel [1 ]
Bargi-Souza, Paula [1 ,2 ]
Kemkem, Yasmine [1 ]
Guillou, Anne [1 ]
Ravier, Magalie A. [1 ]
Bertrand, Gyslaine [1 ]
Varrault, Annie [1 ]
Fiordelisio, Tatiana [1 ,3 ]
Hodson, David J. [4 ]
Mollard, Patrice [1 ]
Schaeffer, Marie [1 ,5 ]
机构
[1] Univ Montpellier, Inst Funct Genom, CNRS, INSERM, Montpellier, France
[2] Fed Univ Minas Gerais UFMG, Inst Biol Sci, Dept Physiol & Biophys, Belo Horizonte, Brazil
[3] Univ Nacl Autonoma Mexico, Fac Ciencias, Lab Neuroendocrinol Comparada, Lab Nacl Soluc Biomimet Diagnost & Terapia LaNSBio, Mexico City, Mexico
[4] Univ Oxford, Churchill Hosp, Natl Inst Hlth & Care Res NIHR, Oxford Ctr Diabet Endocrinol & Metab OCDEM,Oxford, Oxford, England
[5] Univ Montpellier, Ctr Biol Struct, CNRS UMR 5048, INSERM U1054, Montpellier, France
关键词
diabetes; vessel; pericyte; optogenetics; pancreas; imaging; in vivo; BLOOD-FLOW; ENDOTHELIAL-CELLS; BETA-CELLS; GLUCOSE; MICROENVIRONMENT; BRAIN; MODEL; STAR; RAT;
D O I
10.3389/fendo.2022.918733
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pancreatic islets are highly vascularized micro-organs ensuring whole body glucose homeostasis. Islet vascular cells play an integral part in sustaining adequate insulin release by beta cells. In particular, recent studies have demonstrated that islet pericytes regulate local blood flow velocity and are required for maintenance of beta cell maturity and function. In addition, increased metabolic demand accompanying obesity alters islet pericyte morphology. Here, we sought to explore the effects of metabolic stress on islet pericyte functional response to stimulation in a mouse model of type 2 diabetes, directly in the pancreas in vivo . We found that high fat diet induced islet pericyte hypertrophy without alterations in basal local blood flow. However, optogenetic stimulation of pericyte activity revealed impaired islet vascular responses, despite increased expression of genes encoding proteins directly or indirectly involved in cell contraction. These findings suggest that metabolic stress impinges upon islet pericyte function, which may contribute to beta cell failure during T2D.
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页数:10
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