Single ion channel recording in 3D culture of stem cells using patch-clamp technique

• Published in: Biochemical and biophysical research communications Vol. 619; pp. 22 - 26
• Main Authors: Chubinskiy-Nadezhdin, Vladislav I., Sudarikova, Anastasia V., Shorokhova, Mariia A., Vasileva, Valeria Y., Khairullina, Zuleikha M., Negulyaev, Yuri A.
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 03.09.2022
• Subjects: 3D cell culture; Ion channels; Mesenchymal stem cells; Single-channel recording; Spheroids; Stretch-activated channels; 3D cell culture; Single-channel recording; Ion channels; Spheroids; Mesenchymal stem cells; Stretch-activated channels
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2022.06.022

Tri-dimensional (3D) cell aggregates or spheroids are considered to be closer to physiological conditions than traditional 2D cell culture. Mesenchymal stem cells (MSCs) assembling in spheroids have increased the survival of transplanted cells. The organization of stem cells in 3D culture affects cell microenvironment and their mechanical properties. The regulation of the biological processes that maintain crucial physiological reactions of MSCs is closely related to the functioning of ion channels. The pattern of expression, role and regulatory mechanisms of ion channels could be significantly different in 3D compared to 2D culture, and, thus, needed to be properly analyzed on the level of ionic currents. Electrophysiological data on the features of ion channels functioning in 3D cell culture models are currently very limited in the literature. This gap of knowledge may be associated with technical difficulties that exist when researchers try to apply the standard patch clamp method for the registration of ion channels in cells aggregated in spheroids. In this regard, our study focuses on solving emerging technical difficulties and presents an example of their successful solution. Here, we developed a specific approach and have recorded the activity of mechanosensitive stretch-activated ion channels (SACs) in endometrial MSCs (eMSCs) assembled in spheroids. Moreover, we observed functional interplay of SACs with potassium channels of big conductance (BK) in the plasma membrane of eMSC spheroids consistently to revealed earlier in routine 2D cultured cells. Additionally, we observed a significant decrease in the frequency of SACs activation in spheroids that may indicate the differences in the level of functional expression of channels in 3D culture comparing to 2D culture of eMSCs. •A specific protocol for patch formation on 3D culture of stem cells was developed.•The activity of native endogenous ion channels in eMSC from spheroids was recorded.•The differences in SACs activity in 3D comparing to 2D eMSCs culture were identified.•A new approach could be applied for the identification of ion channels in 3D cell cultures.