TY - JOUR
T1 - The function of TRP channels in neutrophil granulocytes
AU - Najder, Karolina
AU - Musset, Boris
AU - Lindemann, Otto
AU - Bulk, Etmar
AU - Schwab, Albrecht
AU - Fels, Benedikt
N1 - Funding Information:
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.
Publisher Copyright:
© 2018, Springer-Verlag GmbH Germany, part of Springer Nature.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2018/7/1
Y1 - 2018/7/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85046126816&partnerID=8YFLogxK
U2 - 10.1007/s00424-018-2146-8
DO - 10.1007/s00424-018-2146-8
M3 - Scientific review articles
C2 - 29717355
AN - SCOPUS:85046126816
SN - 0031-6768
VL - 470
SP - 1017
EP - 1033
JO - Pflugers Archiv European Journal of Physiology
JF - Pflugers Archiv European Journal of Physiology
IS - 7
ER -