Analysis of purine receptor expression and functionality in alveolar epithelial cells

Standard

Analysis of purine receptor expression and functionality in alveolar epithelial cells. / Olotu, Cynthia; Kiefmann, Martina; Ronneburg, Cornelia; Lehmensiek, Felix; Cuvenhaus, Annelie; Meidl, Volker; Goetz, Alwin E; Kiefmann, Rainer.

In: PURINERG SIGNAL, Vol. 16, No. 2, 06.2020, p. 213-229.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Olotu, C, Kiefmann, M, Ronneburg, C, Lehmensiek, F, Cuvenhaus, A, Meidl, V, Goetz, AE & Kiefmann, R 2020, 'Analysis of purine receptor expression and functionality in alveolar epithelial cells', PURINERG SIGNAL, vol. 16, no. 2, pp. 213-229. https://doi.org/10.1007/s11302-020-09696-0

APA

Olotu, C., Kiefmann, M., Ronneburg, C., Lehmensiek, F., Cuvenhaus, A., Meidl, V., Goetz, A. E., & Kiefmann, R. (2020). Analysis of purine receptor expression and functionality in alveolar epithelial cells. PURINERG SIGNAL, 16(2), 213-229. https://doi.org/10.1007/s11302-020-09696-0

Vancouver

Bibtex

@article{a476a65f6a874c41bca74dfcfab75ef7,
title = "Analysis of purine receptor expression and functionality in alveolar epithelial cells",
abstract = "Despite its fundamental role in providing an extensive surface for gas exchange, the alveolar epithelium (AE) serves as an immunological barrier through, e.g., the release of proinflammatory cytokines and secretion of surfactant to prevent alveolar collapse. Thus, AE is important for sustaining lung homeostasis. Extracellular ATP secreted by alveolar epithelial cells (AECs) is involved in physiological and pathological conditions and acts mainly through the activation of purine receptors (P2Rs). When studying P2R-mediated processes, primary isolated type II AECs (piAECs) still represent the gold standard in in vitro research, although their preparation is time-consuming and requires the sacrifice of many animals. Hence, cultivated immortalized and tumor-derived AEC lines may constitute a valuable alternative. In this work, we examined P2R expression and functionality in piAECs, in immortalized and tumor-derived AEC lines with the purpose of gaining a better understanding of purinergic signaling in different cell systems and assisting researchers in the choice of a suitable cell line with a certain P2R in demand. We combined mRNA and protein analysis to evaluate the expression of P2R. For pharmacological testing, we conducted calcium ([Ca2+]) measurements and siRNA receptor knockdown. Interestingly, the mRNA and protein levels of P2Y2, P2Y6, and P2X4 were detected on all cell lines. Concerning functionality, P2XR could be narrowed to L2 and piAECs while P2YR were active in all cell lines.",
author = "Cynthia Olotu and Martina Kiefmann and Cornelia Ronneburg and Felix Lehmensiek and Annelie Cuvenhaus and Volker Meidl and Goetz, {Alwin E} and Rainer Kiefmann",
year = "2020",
month = jun,
doi = "10.1007/s11302-020-09696-0",
language = "English",
volume = "16",
pages = "213--229",
journal = "PURINERG SIGNAL",
issn = "1573-9538",
publisher = "Springer Netherlands",
number = "2",

}

RIS

TY - JOUR

T1 - Analysis of purine receptor expression and functionality in alveolar epithelial cells

AU - Olotu, Cynthia

AU - Kiefmann, Martina

AU - Ronneburg, Cornelia

AU - Lehmensiek, Felix

AU - Cuvenhaus, Annelie

AU - Meidl, Volker

AU - Goetz, Alwin E

AU - Kiefmann, Rainer

PY - 2020/6

Y1 - 2020/6

N2 - Despite its fundamental role in providing an extensive surface for gas exchange, the alveolar epithelium (AE) serves as an immunological barrier through, e.g., the release of proinflammatory cytokines and secretion of surfactant to prevent alveolar collapse. Thus, AE is important for sustaining lung homeostasis. Extracellular ATP secreted by alveolar epithelial cells (AECs) is involved in physiological and pathological conditions and acts mainly through the activation of purine receptors (P2Rs). When studying P2R-mediated processes, primary isolated type II AECs (piAECs) still represent the gold standard in in vitro research, although their preparation is time-consuming and requires the sacrifice of many animals. Hence, cultivated immortalized and tumor-derived AEC lines may constitute a valuable alternative. In this work, we examined P2R expression and functionality in piAECs, in immortalized and tumor-derived AEC lines with the purpose of gaining a better understanding of purinergic signaling in different cell systems and assisting researchers in the choice of a suitable cell line with a certain P2R in demand. We combined mRNA and protein analysis to evaluate the expression of P2R. For pharmacological testing, we conducted calcium ([Ca2+]) measurements and siRNA receptor knockdown. Interestingly, the mRNA and protein levels of P2Y2, P2Y6, and P2X4 were detected on all cell lines. Concerning functionality, P2XR could be narrowed to L2 and piAECs while P2YR were active in all cell lines.

AB - Despite its fundamental role in providing an extensive surface for gas exchange, the alveolar epithelium (AE) serves as an immunological barrier through, e.g., the release of proinflammatory cytokines and secretion of surfactant to prevent alveolar collapse. Thus, AE is important for sustaining lung homeostasis. Extracellular ATP secreted by alveolar epithelial cells (AECs) is involved in physiological and pathological conditions and acts mainly through the activation of purine receptors (P2Rs). When studying P2R-mediated processes, primary isolated type II AECs (piAECs) still represent the gold standard in in vitro research, although their preparation is time-consuming and requires the sacrifice of many animals. Hence, cultivated immortalized and tumor-derived AEC lines may constitute a valuable alternative. In this work, we examined P2R expression and functionality in piAECs, in immortalized and tumor-derived AEC lines with the purpose of gaining a better understanding of purinergic signaling in different cell systems and assisting researchers in the choice of a suitable cell line with a certain P2R in demand. We combined mRNA and protein analysis to evaluate the expression of P2R. For pharmacological testing, we conducted calcium ([Ca2+]) measurements and siRNA receptor knockdown. Interestingly, the mRNA and protein levels of P2Y2, P2Y6, and P2X4 were detected on all cell lines. Concerning functionality, P2XR could be narrowed to L2 and piAECs while P2YR were active in all cell lines.

U2 - 10.1007/s11302-020-09696-0

DO - 10.1007/s11302-020-09696-0

M3 - SCORING: Journal article

C2 - 32236789

VL - 16

SP - 213

EP - 229

JO - PURINERG SIGNAL

JF - PURINERG SIGNAL

SN - 1573-9538

IS - 2

ER -