Optical tools for understanding the complexity of β-cell signalling and insulin release

Following stimulation, pancreatic β-cells must orchestrate a plethora of signalling events to ensure the appropriate release of insulin and maintenance of normal glucose homeostasis. Failure at any point in this cascade leads to impaired insulin secretion, elevated blood levels of glucose and eventu...

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Published inNature reviews. Endocrinology Vol. 14; no. 12; pp. 721 - 737
Main Authors Frank, James A, Broichhagen, Johannes, Yushchenko, Dmytro A, Trauner, Dirk, Schultz, Carsten, Hodson, David J
Format Journal Article
LanguageEnglish
Published England Nature Publishing Group 01.12.2018
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Abstract Following stimulation, pancreatic β-cells must orchestrate a plethora of signalling events to ensure the appropriate release of insulin and maintenance of normal glucose homeostasis. Failure at any point in this cascade leads to impaired insulin secretion, elevated blood levels of glucose and eventually type 2 diabetes mellitus. Likewise, β-cell replacement or regeneration strategies for the treatment of both type 1 and type 2 diabetes mellitus might fail if the correct cell signalling phenotype cannot be faithfully recreated. However, current understanding of β-cell function is complicated because of the highly dynamic nature of their intracellular and intercellular signalling as well as insulin release itself. β-Cells must precisely integrate multiple signals stemming from multiple cues, often with differing intensities, frequencies and cellular and subcellular localizations, before converging these signals onto insulin exocytosis. In this respect, optical approaches with high resolution in space and time are extremely useful for properly deciphering the complexity of β-cell signalling. An increased understanding of β-cell signalling might identify new mechanisms underlying insulin release, with relevance for future drug therapy and de novo stem cell engineering of functional islets.
AbstractList Following stimulation, pancreatic β-cells must orchestrate a plethora of signalling events to ensure the appropriate release of insulin and maintenance of normal glucose homeostasis. Failure at any point in this cascade leads to impaired insulin secretion, elevated blood levels of glucose and eventually type 2 diabetes mellitus. Likewise, β-cell replacement or regeneration strategies for the treatment of both type 1 and type 2 diabetes mellitus might fail if the correct cell signalling phenotype cannot be faithfully recreated. However, current understanding of β-cell function is complicated because of the highly dynamic nature of their intracellular and intercellular signalling as well as insulin release itself. β-Cells must precisely integrate multiple signals stemming from multiple cues, often with differing intensities, frequencies and cellular and subcellular localizations, before converging these signals onto insulin exocytosis. In this respect, optical approaches with high resolution in space and time are extremely useful for properly deciphering the complexity of β-cell signalling. An increased understanding of β-cell signalling might identify new mechanisms underlying insulin release, with relevance for future drug therapy and de novo stem cell engineering of functional islets.
Author Broichhagen, Johannes
Trauner, Dirk
Schultz, Carsten
Frank, James A
Yushchenko, Dmytro A
Hodson, David J
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  surname: Frank
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  orcidid: 0000-0003-3084-6595
  surname: Broichhagen
  fullname: Broichhagen, Johannes
  organization: Department of Chemical Biology, Max Planck Institute for Medical Research, Heidelberg, Germany
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  givenname: Dmytro A
  surname: Yushchenko
  fullname: Yushchenko, Dmytro A
  organization: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic
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  givenname: Dirk
  orcidid: 0000-0002-6782-6056
  surname: Trauner
  fullname: Trauner, Dirk
  organization: Department of Chemistry, New York University, New York, NY, USA
– sequence: 5
  givenname: Carsten
  surname: Schultz
  fullname: Schultz, Carsten
  email: schulcar@ohsu.edu, schulcar@ohsu.edu
  organization: Department of Physiology and Pharmacology, Oregon Health and Science University, Portland, OR, USA. schulcar@ohsu.edu
– sequence: 6
  givenname: David J
  orcidid: 0000-0002-8641-8568
  surname: Hodson
  fullname: Hodson, David J
  email: d.hodson@bham.ac.uk, d.hodson@bham.ac.uk
  organization: Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK. d.hodson@bham.ac.uk
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30356209$$D View this record in MEDLINE/PubMed
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Snippet Following stimulation, pancreatic β-cells must orchestrate a plethora of signalling events to ensure the appropriate release of insulin and maintenance of...
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SubjectTerms Animals
Blood levels
Cell signaling
Diabetes
Diabetes mellitus
Diabetes mellitus (insulin dependent)
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - genetics
Diabetes Mellitus, Type 2 - metabolism
Exocytosis
Genetic Predisposition to Disease - epidemiology
Glucose
Glucose - metabolism
Homeostasis
Homeostasis - genetics
Humans
Incidence
Insulin
Insulin secretion
Insulin Secretion - physiology
Insulin-Secreting Cells - metabolism
Intracellular signalling
Metabolic disorders
Pancreas
Phenotypes
Risk Assessment
Secretion
Sensitivity and Specificity
Signal Transduction
Stem cells
Title Optical tools for understanding the complexity of β-cell signalling and insulin release
URI https://www.ncbi.nlm.nih.gov/pubmed/30356209
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