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Glioblastoma-mesenchymal stem cell communication modulates expression patterns of kinin receptors: Possible involvement of bradykinin in information flow.
Cytometry A 2016; 89(4):365-75C

Abstract

The most aggressive subtype of brain tumors is glioma WHO grade IV, the glioblastoma (GBM). The present work aims to elucidate the role of kinin receptors in interactions between GBM cells and mesenchymal stem cells (MSC). The GBM cell line U87-MG was stably transfected to express dsRed protein, single cell cloned, expanded, and cultured with MSC, both in the direct co-cultures (DC) and indirect co-cultures (IC) at equal cell number ratio for 72 h. Up- and down-regulation of matrix metalloproteases (MMP)-9 expression in U87-MG and MSC cells, respectively, in direct co-culture points to possible MSC participation in tumor invasion. MMP9 expression is in line with significantly increased expression of kinin B1 (B1R) and B2 receptor (B2R) in U87-MG cells and their decreased levels in MSC, as confirmed by quantitative assessment using flow cytometric analysis. Similarly, in indirect cultures (IC), lacking the contact between GBM and MSC cells, an increase of B1 and B2 receptor expression was again noted in U87-MG cells, and no significant changes in kinin receptors in MSC was observed. Functionality of kinin-B1 and B2 receptors was evidenced by stimulation of intracellular calcium fluxes by their respective agonists, des-Arg9-bradykinin (DBK) and bradykinin (BK). Moreover, BK showed a feedback control on kinin receptor expression in mono-cultures, direct and indirect co-cultures. The treatment with BK resulted in down-regulation of B1 and B2 receptors in MSC, with simultaneous up-regulation of these receptors in U87-MG cells, suggesting that functions of BK in information flow between these cells is important for tumor progression and invasion. © 2015 International Society for Advancement of Cytometry.

Authors+Show Affiliations

Department of Biochemistry, Institute of Chemistry, University of São Paulo, Av. Prof. Lineu Prestes 748, São Paulo, S.P, 05508-000, Brazil.Department of Biochemistry, Institute of Chemistry, University of São Paulo, Av. Prof. Lineu Prestes 748, São Paulo, S.P, 05508-000, Brazil.Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ljubljana, Slovenia.Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ljubljana, Slovenia. Nanosciences and Nanotechnologies Programme, Jožef Stefan International Postgraduate School, Jamova 39, Ljubljana, 1000, Slovenia.Department of Biochemistry, Institute of Chemistry, University of São Paulo, Av. Prof. Lineu Prestes 748, São Paulo, S.P, 05508-000, Brazil.Department of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ljubljana, Slovenia. Nanosciences and Nanotechnologies Programme, Jožef Stefan International Postgraduate School, Jamova 39, Ljubljana, 1000, Slovenia.Department of Biochemistry, Institute of Chemistry, University of São Paulo, Av. Prof. Lineu Prestes 748, São Paulo, S.P, 05508-000, Brazil.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

26671187

Citation

Pillat, Micheli M., et al. "Glioblastoma-mesenchymal Stem Cell Communication Modulates Expression Patterns of Kinin Receptors: Possible Involvement of Bradykinin in Information Flow." Cytometry. Part a : the Journal of the International Society for Analytical Cytology, vol. 89, no. 4, 2016, pp. 365-75.
Pillat MM, Oliveira MN, Motaln H, et al. Glioblastoma-mesenchymal stem cell communication modulates expression patterns of kinin receptors: Possible involvement of bradykinin in information flow. Cytometry A. 2016;89(4):365-75.
Pillat, M. M., Oliveira, M. N., Motaln, H., Breznik, B., Glaser, T., Lah, T. T., & Ulrich, H. (2016). Glioblastoma-mesenchymal stem cell communication modulates expression patterns of kinin receptors: Possible involvement of bradykinin in information flow. Cytometry. Part a : the Journal of the International Society for Analytical Cytology, 89(4), pp. 365-75. doi:10.1002/cyto.a.22800.
Pillat MM, et al. Glioblastoma-mesenchymal Stem Cell Communication Modulates Expression Patterns of Kinin Receptors: Possible Involvement of Bradykinin in Information Flow. Cytometry A. 2016;89(4):365-75. PubMed PMID: 26671187.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Glioblastoma-mesenchymal stem cell communication modulates expression patterns of kinin receptors: Possible involvement of bradykinin in information flow. AU - Pillat,Micheli M, AU - Oliveira,Mona N, AU - Motaln,Helena, AU - Breznik,Barbara, AU - Glaser,Talita, AU - Lah,Tamara T, AU - Ulrich,Henning, Y1 - 2015/12/15/ PY - 2015/06/17/received PY - 2015/10/08/revised PY - 2015/11/03/accepted PY - 2015/12/17/entrez PY - 2015/12/17/pubmed PY - 2017/10/25/medline KW - Bradykinin KW - bone-marrow mesenchymal stem cells KW - direct and indirect cell co-culture KW - glioblastoma KW - kinin-B1 receptor KW - kinin-B2 receptor SP - 365 EP - 75 JF - Cytometry. Part A : the journal of the International Society for Analytical Cytology JO - Cytometry A VL - 89 IS - 4 N2 - The most aggressive subtype of brain tumors is glioma WHO grade IV, the glioblastoma (GBM). The present work aims to elucidate the role of kinin receptors in interactions between GBM cells and mesenchymal stem cells (MSC). The GBM cell line U87-MG was stably transfected to express dsRed protein, single cell cloned, expanded, and cultured with MSC, both in the direct co-cultures (DC) and indirect co-cultures (IC) at equal cell number ratio for 72 h. Up- and down-regulation of matrix metalloproteases (MMP)-9 expression in U87-MG and MSC cells, respectively, in direct co-culture points to possible MSC participation in tumor invasion. MMP9 expression is in line with significantly increased expression of kinin B1 (B1R) and B2 receptor (B2R) in U87-MG cells and their decreased levels in MSC, as confirmed by quantitative assessment using flow cytometric analysis. Similarly, in indirect cultures (IC), lacking the contact between GBM and MSC cells, an increase of B1 and B2 receptor expression was again noted in U87-MG cells, and no significant changes in kinin receptors in MSC was observed. Functionality of kinin-B1 and B2 receptors was evidenced by stimulation of intracellular calcium fluxes by their respective agonists, des-Arg9-bradykinin (DBK) and bradykinin (BK). Moreover, BK showed a feedback control on kinin receptor expression in mono-cultures, direct and indirect co-cultures. The treatment with BK resulted in down-regulation of B1 and B2 receptors in MSC, with simultaneous up-regulation of these receptors in U87-MG cells, suggesting that functions of BK in information flow between these cells is important for tumor progression and invasion. © 2015 International Society for Advancement of Cytometry. SN - 1552-4930 UR - https://www.unboundmedicine.com/medline/citation/26671187/Glioblastoma_mesenchymal_stem_cell_communication_modulates_expression_patterns_of_kinin_receptors:_Possible_involvement_of_bradykinin_in_information_flow_ L2 - https://doi.org/10.1002/cyto.a.22800 DB - PRIME DP - Unbound Medicine ER -