Co-storage and release of insulin-like peptide-5, glucagon-like peptide-1 and peptideYY from murine and human colonic enteroendocrine cells

被引:49
作者
Billing, Lawrence J. [1 ,2 ]
Smith, Christopher A. [1 ,2 ]
Larraufie, Pierre [1 ,2 ]
Goldspink, Deborah A. [1 ,2 ]
Galvin, Sam [1 ,2 ]
Kay, Richard G. [1 ,2 ]
Howe, Jonathan D. [3 ]
Walker, Ryan [1 ,2 ]
Pruna, Mihai [1 ,2 ]
Glass, Leslie [1 ,2 ]
Pais, Ramona [1 ,2 ]
Gribble, Fiona M. [1 ,2 ]
Reimann, Frank [1 ,2 ]
机构
[1] Univ Cambridge, Inst Metab Sci, Cambridge CB0 0QQ, England
[2] Univ Cambridge, MRC Metab Dis Unit, Cambridge CB0 0QQ, England
[3] MRC Lab Mol Biol, Cambridge CB2 0QH, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
Insulin-like peptide-5 (INSL5); Glucagon-like peptide-1 (GLP-1); peptideYY (PYY); Enteroendocrine; L-cell; LC-MS; Human colonic cultures; 3D-SIM; PYY SECRETION; GLP-1; MICE; YY; SUPERRESOLUTION; COLOCALIZATION; PROTEINS; HORMONES; INSL5;
D O I
10.1016/j.molmet.2018.07.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Insulin-like peptide-5 (INSL5) is an orexigenic gut hormone found in a subset of colonic and rectal enteroendocrine L-cells together with the anorexigenic hormones glucagon-like peptide-1 (GLP-1) and peptideYY (PYY). Unlike GLP-1 and PYY, INSL5 levels are elevated by calorie restriction, raising questions about how these hormones respond to different stimuli when they arise from the same cell type. The aim of the current study was to identify whether and how INSL5, GLP-1 and PYY are co-secreted or differentially secreted from colonic L-cells. Methods: An inducible reporter mouse (Insl5-rtTA) was created to enable selective characterisation of Insl5-expressing cells. Expression profiling and Ca2+-dynamics were assessed using TET-reporter mice. Secretion of INSL5, PYY, and GLP-1 from murine and human colonic crypt cultures was quantified by tandem mass spectrometry. Vesicular co-localisation of the three hormones was analysed in 3D-SIM images of immunofluorescently-labelled murine colonic primary cultures and tissue sections. Results: INSL5-producing cells expressed a range of G-protein coupled receptors previously identified in GLP-1 expressing L-cells, including Ffar1, Gpbar1, and Agtr1a. Pharmacological or physiological agonists for these receptors triggered Ca2+ transients in INSL5-producing cells and stimulated INSL5 secretion. INSL5 secretory responses strongly correlated with those of PYY and GLP-1 across a range of stimuli. The majority (>80%) of secretory vesicles co-labelled for INSL5, PYY and GLP-1. Conclusions: INSL5 is largely co-stored with PYY and GLP-1 and all three hormones are co-secreted when INSL5-positive cells are stimulated. Opposing hormonal profiles observed in vivo likely reflect differential stimulation of L-cells in the proximal and distal gut. (C) 2018 The Authors. Published by Elsevier GmbH.
引用
收藏
页码:65 / 75
页数:11
相关论文
共 31 条
[1]   KiT: a MATLAB package for kinetochore tracking [J].
Armond, Jonathan W. ;
Vladimirou, Elina ;
McAinsh, Andrew D. ;
Burroughs, Nigel J. .
BIOINFORMATICS, 2016, 32 (12) :1917-1919
[2]   Bile Acids Trigger GLP-1 Release Predominantly by Accessing Basolaterally Located G Protein-Coupled Bile Acid Receptors [J].
Brighton, Cheryl A. ;
Rievaj, Juraj ;
Kuhre, Rune E. ;
Glass, Leslie L. ;
Schoonjans, Kristina ;
Holst, Jens J. ;
Gribble, Fiona M. ;
Reimann, Frank .
ENDOCRINOLOGY, 2015, 156 (11) :3961-3970
[3]   Ultrasensitive fluorescent proteins for imaging neuronal activity [J].
Chen, Tsai-Wen ;
Wardill, Trevor J. ;
Sun, Yi ;
Pulver, Stefan R. ;
Renninger, Sabine L. ;
Baohan, Amy ;
Schreiter, Eric R. ;
Kerr, Rex A. ;
Orger, Michael B. ;
Jayaraman, Vivek ;
Looger, Loren L. ;
Svoboda, Karel ;
Kim, Douglas S. .
NATURE, 2013, 499 (7458) :295-+
[4]   Glucagon-like peptide 1 and peptide YY are in separate storage organelles in enteroendocrine cells [J].
Cho, Hyun-Jung ;
Robinson, Eliza S. ;
Rivera, Leni R. ;
McMillan, Paul J. ;
Testro, Adam ;
Nikfarjam, Mehrdad ;
Bravo, David M. ;
Furness, John B. .
CELL AND TISSUE RESEARCH, 2014, 357 (01) :63-69
[5]   Gut Hormones and Appetite Control: A Focus on PYY and GLP-1 as Therapeutic Targets in Obesity [J].
De Silva, Akila ;
Bloom, Stephen R. .
GUT AND LIVER, 2012, 6 (01) :10-20
[6]   Gpr40 is expressed in enteroendocrine cells and mediates free fatty acid stimulation of incretin secretion [J].
Edfalk, Sara ;
Steneberg, Par ;
Edlund, Helena .
DIABETES, 2008, 57 (09) :2280-2287
[7]   Costorage of Enteroendocrine Hormones Evaluated at the Cell and Subcellular Levels in Male Mice [J].
Fothergill, Linda J. ;
Callaghan, Brid ;
Hunne, Billie ;
Bravo, David M. ;
Furness, John B. .
ENDOCRINOLOGY, 2017, 158 (07) :2113-2123
[8]   Single-cell RNA-sequencing reveals a distinct population of proglucagon-expressing cells specific to the mouse upper small intestine [J].
Glass, Leslie L. ;
Calera-Nieto, Fernando J. ;
Jawaid, Wajid ;
Larraufle, Pierre ;
Kay, Richard G. ;
Gottgens, Berthold ;
Relmann, Frank ;
Gribble, Fiona M. .
MOLECULAR METABOLISM, 2017, 6 (10) :1296-1303
[9]   Insulin-like peptide 5 is an orexigenic gastrointestinal hormone [J].
Grosse, Johannes ;
Heffron, Helen ;
Burling, Keith ;
Hossain, Mohammed Akhter ;
Habib, Abdella M. ;
Rogers, Gareth J. ;
Richards, Paul ;
Larder, Rachel ;
Rimmington, Debra ;
Adriaenssens, Alice A. ;
Parton, Laura ;
Powell, Justin ;
Binda, Matteo ;
Colledge, William H. ;
Doran, Joanne ;
Toyoda, Yukio ;
Wade, John D. ;
Aparicio, Samuel ;
Carlton, Mark B. L. ;
Coll, Anthony P. ;
Reimann, Frank ;
O'Rahilly, Stephen ;
Gribble, Fiona M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (30) :11133-11138
[10]   Neurotensin Is Coexpressed, Coreleased, and Acts Together With GLP-1 and PYY in Enteroendocrine Control of Metabolism [J].
Grunddal, Kaare V. ;
Ratner, Cecilia F. ;
Svendsen, Berit ;
Sommer, Felix ;
Engelstoft, Maja S. ;
Madsen, Andreas N. ;
Pedersen, Jens ;
Nohr, Mark K. ;
Egerod, Kristoffer L. ;
Nawrocki, Andrea R. ;
Kowalski, Timothy ;
Howard, Andrew D. ;
Poulsen, Steen Seier ;
Offermanns, Stefan ;
Backhed, Fredrik ;
Holst, Jens J. ;
Holst, Birgitte ;
Schwartz, Thue W. .
ENDOCRINOLOGY, 2016, 157 (01) :176-194