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The function of TRP channels in neutrophil granulocytes

  • Karolina Najder
  • Boris Musset
  • Otto Lindemann
  • Etmar Bulk
  • Albrecht SchwabEmail author
  • Benedikt Fels
Invited Review
Part of the following topical collections:
  1. Invited Review

Abstract

Neutrophil granulocytes are exposed to widely varying microenvironmental conditions when pursuing their physiological or pathophysiological functions such as fighting invading bacteria or infiltrating cancer tissue. Examples for harsh environmental challenges include among others mechanical shear stress during the recruitment from the vasculature or the hypoxic and acidotic conditions within the tumor microenvironment. Chemokine gradients, reactive oxygen species, pressure, matrix elasticity, and temperature can be added to the list of potential challenges. Transient receptor potential (TRP) channels serve as cellular sensors since they respond to many of the abovementioned environmental stimuli. The present review investigates the role of TRP channels in neutrophil granulocytes and their role in regulating and adapting neutrophil function to microenvironmental cues. Following a brief description of neutrophil functions, we provide an overview of the electrophysiological characterization of neutrophilic ion channels. We then summarize the function of individual TRP channels in neutrophil granulocytes with a focus on TRPC6 and TRPM2 channels. We close the review by discussing the impact of the tumor microenvironment of pancreatic ductal adenocarcinoma (PDAC) on neutrophil granulocytes. Since neutrophil infiltration into PDAC tissue contributes to disease progression, we propose neutrophilic TRP channel blockade as a potential therapeutic option.

Keywords

Calcium Cell migration Cell signaling Neutrophil granulocyte Pancreas TRP channels 

Notes

Acknowledgements

The authors wish to thank past and present members of their laboratories whose enthusiastic work contributed largely to developing the concepts described in this review.

Funding information

K.N. is supported by a fellowship from the CIM-IMPRS graduate school. A.S. thanks the support from the Deutsche Forschungsgemeinschaft (DFG; SCHW 407/17-1), Cells-in-Motion Cluster of Excellence (EXC 1003-CiM), University of Münster, Germany, and IZKF Münster (Schw2/020/18). B.F. received support from Cells-in-Motion Cluster of Excellence (EXC 1003-CiM; PP 2016-12), and B.M. is supported by DFG grant MU 3574/4-1.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  • Karolina Najder
    • 1
  • Boris Musset
    • 2
  • Otto Lindemann
    • 1
  • Etmar Bulk
    • 1
  • Albrecht Schwab
    • 1
    Email author
  • Benedikt Fels
    • 1
  1. 1.Institut für Physiologie IIMünsterGermany
  2. 2.Institut für PhysiologieParacelsus Medizinische PrivatuniversitätNürnbergGermany

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