A chip device to determine surface charge properties of confluent cell monolayers by measuring streaming potential

被引:21
作者
Kincses, Andras [1 ,2 ]
Santa-Maria, Ana R. [1 ,3 ]
Walter, Fruzsina R. [1 ,4 ]
Der, Laszlo [1 ]
Horanyi, Nora [1 ]
Lipka, Dora V. [1 ]
Valkai, Sandor [1 ]
Deli, Maria A. [1 ]
Der, Andras [1 ]
机构
[1] Biol Res Ctr, Inst Biophys, Szeged, Hungary
[2] Univ Szeged, Doctoral Sch Multidisciplinary Med Sci, Szeged, Hungary
[3] Univ Szeged, Doctoral Sch Biol, Szeged, Hungary
[4] Univ Szeged, Dept Cell Biol & Mol Med, Szeged, Hungary
基金
欧盟地平线“2020”;
关键词
BLOOD-BRAIN-BARRIER; IN-VITRO MODEL; TIGHT JUNCTION; PERMEABILITY; CACO-2; FLOW;
D O I
10.1039/d0lc00558d
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cell surface charge is an important element of the function of biological barriers, but no chip device has been described to measure cell surface charge properties of confluent barrier cell monolayers. The aim of this study was the design and fabrication of a dynamic lab-on-a-chip (LOC) device which is suitable to monitor transcellular electrical resistance, as well as streaming potential parallel to the surface of cell layers. We successfully measured the streaming potential of a biological barrier culture model with the help of our previously published versatile lab-on-a-chip device equipped with two Ag/AgCl electrodes. The inclusion of these "zeta electrodes", a voltage preamplifier and an oscilloscope in our set-up made it possible to successfully record signals describing the surface charge properties of brain endothelial cell monolayers, used as a barrier model in our experiments. Data obtained on the new chip device were verified by comparing streaming potential results measured in the LOC device and zeta potential results by the commonly used laser-Doppler velocimetry (LDv) method and model simulations. Changes in the negative surface charge of the barrier model by treatments with neuraminidase enzyme modifying the cell membrane glycocalyx or lidocaine altering the lipid membrane charge could be measured by both the upgraded LOC device and LDv. The new chip device can help to gain meaningful new information on how surface charge is linked to barrier function in both physiological and pathological conditions.
引用
收藏
页码:3792 / 3805
页数:14
相关论文
共 60 条
[1]   Structure and function of the blood-brain barrier [J].
Abbott, N. Joan ;
Patabendige, Adjanie A. K. ;
Dolman, Diana E. M. ;
Yusof, Siti R. ;
Begley, David J. .
NEUROBIOLOGY OF DISEASE, 2010, 37 (01) :13-25
[2]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[3]   Brain-Specific Ultrastructure of Capillary Endothelial Glycocalyx and Its Possible Contribution for Blood Brain Barrier [J].
Ando, Yoshiaki ;
Okada, Hideshi ;
Takemura, Genzou ;
Suzuki, Kodai ;
Takada, Chihiro ;
Tomita, Hiroyuki ;
Zaikokuji, Ryogen ;
Hotta, Yasuaki ;
Miyazaki, Nagisa ;
Yano, Hirohisa ;
Muraki, Isamu ;
Kuroda, Ayumi ;
Fukuda, Hirotsugu ;
Kawasaki, Yuki ;
Okamoto, Haruka ;
Kawaguchi, Tomonori ;
Watanabe, Takatomo ;
Doi, Tomoaki ;
Yoshida, Takahiro ;
Ushikoshi, Hiroaki ;
Yoshida, Shozo ;
Ogura, Shinji .
SCIENTIFIC REPORTS, 2018, 8
[4]   Impedance-based cell monitoring: Barrier properties and beyond [J].
Benson K. ;
Cramer S. ;
Galla H.-J. .
Fluids and Barriers of the CNS, 10 (1)
[5]   Sialic acids regulate microvessel permeability, revealed by novel in vivo studies of endothelial glycocalyx structure and function [J].
Betteridge, Kai B. ;
Arkill, Kenton P. ;
Neal, Christopher R. ;
Harper, Steven J. ;
Foster, Rebecca R. ;
Satchell, Simon C. ;
Bates, David O. ;
Salmon, Andrew H. J. .
JOURNAL OF PHYSIOLOGY-LONDON, 2017, 595 (15) :5015-5035
[6]   Characterization of a microfluidic in vitro model of the blood-brain barrier (μBBB) [J].
Booth, Ross ;
Kim, Hanseup .
LAB ON A CHIP, 2012, 12 (10) :1784-1792
[7]   Role of the Blood-Brain Barrier in the Nutrition of the Central Nervous System [J].
Campos-Bedolla, Patricia ;
Walter, Fruzsina R. ;
Veszelka, Szilvia ;
Deli, Maria A. .
ARCHIVES OF MEDICAL RESEARCH, 2014, 45 (08) :610-638
[8]   Tight junction and polarity interaction in the transporting epithelial phenotype [J].
Cereijido, Marcelino ;
Contreras, Ruben G. ;
Shoshani, Liora ;
Flores-Benitez, David ;
Larre, Isabel .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2008, 1778 (03) :770-793
[9]   A new dynamic in vitro modular capillaries-venules modular system: Cerebrovascular physiology in a box [J].
Cucullo, Luca ;
Hossain, Mohammed ;
Tierney, William ;
Janigro, Damir .
BMC NEUROSCIENCE, 2013, 14
[10]   Permeability studies on in vitro blood-brain barrier models: Physiology, pathology, and pharmacology [J].
Deli, MA ;
Abraham, CS ;
Kataoka, Y ;
Niwa, M .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2005, 25 (01) :59-127