Features of primary hippocampal cultures formation on scaffolds based on hyaluronic acid glycidyl methacrylate Текст научной статьи по специальности «Фундаментальная медицина»

Features of Primary Hippoca on Scaffolds Based on Hyaluronic Glycidyl Methacrylate

DOI: 10.17691/stm2018.10.1.13 Received October 25, 2017

T.A. Mishchenko, PhD, Senior Researcher, Laboratory for Neuroprotection Methods I Center for Translational Technologies1; Senior Researcher, Molecular and Cell Technologif Central Scientific Research Laboratory2;

E.V. Mitroshina, PhD, Associate Professor, Department of Neurotechnologies, Institute of Bio and Biomedicine1; Senior Researcher, Laboratory for Neuroprotection Methods Development, Center for Translational Technologies1; Senior Researcher, Molecular and Cell Technologies Departmen Central Scientific Research Laboratory2;

A.I. Kuznetsova, Student, Department of Neurotechnologies, Institute of Biology and Biomedicine1; O.M. Shirokova, Junior Researcher, Electron Microscopy Department, Central Scientific Research Laboratory2; E.V. Khaydukov, PhD, Head of Laboratory of Laser Biomedicine3; Head of Laboratory of Photon Bioengineering4;

A.G. Savelyev, PhD Student, Junior Researcher, Laboratory of Laser Biomedicine3; Junior Researcher, Laboratory of Photonic Bioengineering4;

V.K. Popov, DSc, Head of the Supercritical Fluid Technology Laboratory3;

A.V. Zvyagin, DSc, Leading Researcher, Laboratory of Optical Theranostics, Institute of Biology

and Biomedicine1; Director of the Centre of Biomedical Engineering, Institute of Molecular Medicine4;

Associate Professor, Head of the Optical Biomedical Imaging and Sensing Group, ARC Centre of Excellence

for Nanoscale BioPhotonics (CNBP)5;

M.V. Vedunova, DSc, Leading Researcher, Director of the Institute of Biology and Biomedicine1

1Lobachevsky State University of Nizhni Novgorod, 23 Prospekt Gagarina, Nizhny Novgorod, 603950, Russia; 2Privolzhsky Research Medical University, 10/1 Minin and Pozharsky Square, Nizhny Novgorod, 603005, Russia; 3Federal Scientific Research Centre "Crystallography and Photonics", Russian Academy of Sciences, 59 Leninskiy Prospekt, Moscow, 119333, Russia;

4I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya St., Moscow, 119991, Russia; 5Macquarie University, Balaclava Road, North Ryde NSW, Sydney, 2109, Australia

The aim of the study was to investigate the morphological and metabolic features of primary hippocampal cultures formation on hydrogel films and scaffolds based on hyaluronic acid glycidyl methacrylate.

Materials and Methods. Hydrogel films and scaffolds with certain architectonics were developed by micromolding technique on the basis of hyaluronic acid glycidyl methacrylate. Primary hippocampal cells obtained from С57ВL/6 mouse embryos (E18) were cultured on the created constructs more than 14 days. Testing cell viability, morphometric assessment, and analysis of spontaneous calcium activity of primary hippocampal cultures were performed on day 14 of cultures development in vitro.

Results. This study revealed that the material for the development of scaffolds with given architectonics is non-toxic for the nervous system cells. Dissociated hippocampal cells were actively attached to the scaffold surface and were assembled into cell conglomerates, which exhibited spontaneous calcium activity.

Conclusion. Scaffolds designed on the basis of hyaluronic acid glycidyl methacrylate have a high biocompatibility with the nervous system cells. Architectonics and adhesive properties of scaffold contribute to the formation of functionally active cell conglomerates.

Key words: scaffold; hyaluronic acid; biocompatibility; calcium imaging; primary hippocampal cultures.

How to cite: Mishchenko T.A., Mitroshina Е.V., Kuznetsova A.I., Shirokova O.M., Khaydukov E.V., Savelyev A.G., Popov V.K., Zvyagin A.V., Vedunova M.V. Features of primary hippocampal cultures formation on scaffolds based on hyaluronic acid glycidyl methacrylate. Sovremennye tehnologii v medicine 2018; 10(1): 103-110, https://doi.org/10.17691/stm2018.10.1.13

Corresponding author: Tatiana A. Mishchenko, e-mail: saHarnova87@mail.ru

Особенности формирования первичных культур клеток гиппокампа на скаффолдах, полученных из метакрилированной гиалуроновой кислоты

Цель исследования — изучение морфологических и метаболических особенностей формирования первичных культур клеток гиппокампа на гидрогелевых пленках и скаффолдах, полученных на основе метакрилированной гиалуроновой кислоты.

Материалы и методы. На основе метакрилированной гиалуроновой кислоты методом микромолдинга изготовлены гидроге-левые пленки и скаффолды заданной архитектоники. Диссоциированные клетки гиппокампа полученные от 18-дневных эмбрионов мыши линии С57ВL/6 культивировали на разработанных конструктах более 14 дней. На 14-й день культивирования проводили морфометрический анализ, оценку жизнеспособности и анализ спонтанной кальциевой активности первичных гиппокампальных культур.

Результаты. Установлено, что материал, применяемый для разработки скаффолда заданной архитектоники, не токсичен для клеток нервной системы. Диссоциированные клетки гиппокампа активно прикреплялись на поверхность скаффолда и образовывали клеточные конгломераты, проявляющие спонтанную кальциевую активность.

Заключение. Скаффолды, созданные на основе метакрилированной гиалуроновой кислоты, обладают высокой биосовместимостью с клетками нервной системы. Архитектоника и адгезивные свойства скаффолда способствуют формированию функционально активных клеточных конгломератов.

Ключевые слова: скаффолд; гиалуроновая кислота; биосовместимость; кальциевый имиджинг; первичные культуры клеток гиппокампа.

Russian

Introduction

In recent decades, there has been a growing interest in research and development of high-efficiency methods for morphological and functional brain tissue reconstruction. Loss of structural and functional elements of the central nervous system due to the development of pathological processes induced by trauma or diseases with various etiology (ischemia, neoplasm, neurodegenerative diseases, etc.), entails growth of an acute neurological deficit, violations in mnestic and cognitive functions that leads to severe patient disability. Engineering reconstruction of nervous tissue is necessary not only for negation the induced pathological changes but also for stimulation endogenous neuroreparative processes in the damaged area [1-5]. The effectiveness of using three-dimensional constructs (scaffolds) for replacement therapy after a spinal cord injury, in bone and cartilage tissue reparation was already shown [6-10].

Application of three-dimensional constructs with a given architectonics for brain injury correction also seems promising. Strict requirements imposed on materials of scaffolds for neurotransplantation are the absence of cytotoxicity, provision of cell adhesion, proliferation or differentiation. In addition, the material should be efficiently degraded without forming toxic products. These conditions are necessary to minimize risk of neurotransplant rejection and to maintain certain anatomical structure in the lesion focus for providing free transport of biological fluids and its gradual substitution with a natural tissue [3, 5, 11, 12].

Hyaluronic acid is regarded as a potent material for the development of biocompatible three-dimensional constructs [13-16]. Recent studies have shown that hyaluronic acid is an active component of a brain extracellular matrix, which not only structures the nervous tissue but also actively participates in synaptic plasticity, neuronal outgrowth, and cell migration [17-18].

In this regard, the aim of the study was to investigate the morphological and metabolic features of primary hippocampal cultures formation on hydrogel films and scaffolds based on hyaluronic acid glycidyl methacrylate.

Materials and Methods

Formation of hydrogel films. Spacers (thickness 150 |jm) were imposed on coverslip. Photocurable composition consisting of 22% hyaluronic acid glycidyl methacrylate, 2% poly(ethylene glycol) diacrylate (Mn=575) (Sigma Aldrich, USA), 0.005% riboflavin mononucleotide dissolved in 2% collagen solution (Belcozin, Russia) was placed between spacers and then top covered with the second coverslip. The exposure was conducted at 450 nm wavelength (intensity 70 mW/cm2) for 20 min. Then the coverslips were carefully separated. The sample was treated with ultraviolet (intensity 10 mW/cm2). The obtained sample was stored in phosphate buffered saline before the cell culturing.

Fabrication of scaffolds. For the preparation of photocurable composition, 20 wt% hyaluronic acid glycidyl methacrylate (>4 MDa), 2.5 wt% poly(ethylene glycol) diacrylate (Sigma Aldrich, USA), 0.0004 wt%

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104 СТМ J 2018 — V0l. 10, No.1 T.A. Mishchenko, E.V. Mitroshina, A.I. Kuznetsova, O.M. Shirokova, E.V. Khaydukov, ..., M.V. Vedunova

riboflavin mononucleotide were dissolved in 2% collagen solution (Belcozin, Russia) under sonication during 30 min. Thereafter, the composition was incubated at room temperature for 12 h and then placed in ultrasonic bath until formation of uniform consistency.

Scaffolds were produced using micromolding technique [19]. Photocurable composition was placed in a specially made silicone master mold and covered with a coverslip. The exposure was carried out for 20 min using the light emitting diode at 365 nm wavelength (intensity 20 mW/cm2). Then the coverslip was carefully removed and the crosslinked hydrogel scaffold was pulled out from the master mold and placed in a phosphate buffered saline before the cell culturing (Figure 1).

Primary hippocampal cultures were obtained according to the previously developed technique from C57BL/6 mouse embryos (E18) [20]. The main rules of keeping and caring for experimental animals corresponded to the norms provided in the order of the Ministry of Health of the Russian Federation No.708n dated 23.08.2010 "Concerning Approval of the Rules for Laboratory Practice in Russian Federation" and the ethical principles established by European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes (Strasbourg, 2006) and approved by the Ethics Committee of Lobachevsky State University of Nizhni Novgorod.

After enzymatic digestion of hippocampal tissue by 0.25% trypsin solution (Life Technologies, USA) cells were resuspended in Neurobasal™ (Thermo Fisher Scientific, USA) containing B27 supplement (Thermo Fisher Scientific, USA), L-glutamine (Thermo Fisher Scientific, USA), and fetal bovine serum (PanEco, Russia) and then were centrifuged at 1000 rpm within 3 min. The cells were subsequently seeded on hydrogel films and scaffolds in approximate initial density of the cells — 9000 cells/mm2. In control cultures, the same concentration of cells was placed on culture dish and coverslips (18*18 mm) pre-treated by polyethyleneimine (PEI) for increasing cell adhesion. The viability of the primary hippocampal cultures was maintained under the constant conditions of 35.5°C, 5% CO2 and a humidified atmosphere in a cell culture incubator. All experimental cultures were divided into the following groups: "Control 1" — primary hippocampal cultures, obtained by the standard protocol with using specific adhesive substance PEI; "Control 2" — primary hippocampal cultures, cultivated on culture dish without PEI; primary hippocampal cultures cultured on hydrogel films; primary hippocampal cultures cultured on scaffolds.

The viability of primary hippocampal cells were estimated on day 14 of culture development in vitro (DIV) by counting in a inverted fluorescence microscope Leica DMIL HC (Leica, Germany) the number of cell nuclei stained by propidium iodide (Sigma, USA) (dead cells) and the number of cell nuclei stained by bis-benzimide (Sigma, USA) (all cells in a culture). The proportion of dead cells was calculated as the percentage ratio

Figure 1. Representative microscopy imaging of scaffold based on hyaluronic acid glycidyl methacrylate. Scale bar is 250

between bis-benzimide-positive and propidium iodide-positive cells [20].

To investigate the features of metabolic activity of primary hippocampal cell cultures a method of functional calcium imaging was used. Detection of calcium events was performed by using a specific calcium-sensitive dye Oregon Green 488 BAPTA-1 AM (Invitrogen, USA) and a confocal laser-scanning microscope Zeiss LSM 510 (Zeiss, Germany). The time series of the fluorescent images were registered. Determination and analysis of calcium events were conducted in original software Astroscanner (registration certificate for computer program No.20114662670). It was analyzed the records of the F(t) function of the average fluorescence intensity of calcium-sensitive dye in selected region (coinciding with the cell body) from time. To determine the start time (Tstart) and the end time (Tend) of the oscillations, the deviation threshold of the fluorescence level was taken from the mean value at the size of the standard quadratic error F(t). The following parameters were analyzed: the duration of the calcium oscillations (s), the frequency of the calcium oscillations (the number of oscillations per minute), and the percentage of cells exhibited calcium activity [21].

Scanning electron microscopy. This part of the study was carried out on the equipment of the Collective Usage Center "New Materials and Resource-saving Technologies" (Lobachevsky State University of Nizhni Novgorod). Experimental samples were placed in 2.5% glutaraldehyde solution for 12 h at 4°C. After fixation, the samples were washed in 0.01 M phosphate buffered saline (pH 7.4) (Sigma, USA) and then consistently dehydrated at 4°C in a battery of aqueous ethanol solution at increasing concentration: 30, 50, 70, 90, 100%. To remove ethanol, the samples were placed in hexamethyldisilazane (Sigma Aldrich, USA) for 30 min and then were dried in air. The samples were examined

in an electronic scanning microscope JEOL JSM-IT300 (Jeol, Japan). Two types of signal were detected: the backscattered electrons and the secondary electron. In freeware ImageJ, the surface area of individual cells and their conglomerates (|jm2) and the Feret diameter (jm) (maximum distance between the edges of cell body) were calculated.

Statistical analysis. All quantified data are presented as the mean ± standard error of the mean (SEM). Statistical analyses were performed using ANOVA implemented in the Sigma Plot 11.0 software (Systat Software, Inc.). Differences between groups were considered significant if the corresponding p-value was less than 0.05.

Results

One of the key requirements offered for developing scaffold for neurotransplantation is the absence of cytotoxicity of material for the nervous system cells. Thus, the first stage of the research dedicated to the toxicity assessment of hydrogel films based on hyaluronic acid glycidyl methacrylate for primary hippocampal cultures. It was shown the intensive attachment of the dissociated hippocampal cells to the culture dish near the hydrogel film during the first day of culture development in vitro. Further observations revealed the formation of neuronal and glial outgrowth, that during the cultivation transformed into complex intertwined structures, evidencing the creation of a network-like structure (Figure 2). Neurons and glial cells had a typical structure in the field of view there were no cells with morphopathology (rounded, swollen or cells without outgrowth). Directly on the experimental material, a fewer number of cells that formed cellular conglomerates were visualized. Similar conglomerates, but in greater number, were observed in the PEI-

untreated group of cultures ("Control 2"). It is assumed that low concentration of cells on the material is mediated by the lack of architectonics facilitated the effective cell attachment to the hydrogel film.

Cell viability assessment on 14 DIV did not reveal significant differences in the number of dead cells relative to control groups of cultures. The percentage of living cells in the "Control" 1 was 97.0±2.3%, in "Control 2" — 94.0±3.5%, in the experimental group — 95.0±1.9%. Thus it was shown that the tested material is non-toxic for the nervous system cells.

Based on hyaluronic acid glycidyl methacrylate we produced scaffolds with given architectonics (the main parameters and method of preparation are described in "Materials and Methods") on which further cultivation of primary hippocampal cultures was conducted.

We found that scaffolds have more adhesive properties compared with hydrogel films. During the first 24 h of cultivation, the dissociated hippocampal cells were actively attached to the scaffold surface. Neuronal and glial cells were assembled into clusters, which subsequently formed the cell conglomerates (see Figure 2). These conglomerates were connected to each other by complex plexuses of neuronal and glial outgrowth but in a fewer number than conglomerates in the "Control 2" group.

Electron scanning microscopy data revealed that morphometric parameters of single cell and cell conglomerates formed on scaffold had some differences from the parameters of the "Control 2" group (Figure 3). On the background of indistinguishable Feret diameter ("Control 2" — 11.77±0.44 jm, "Scaffold" — 10.84±0.39 jm), the surface area of single cells and the surface area of cell conglomerates were statistically lower than in the control group of cultures (See the Table) (p<0.05, ANOVA).

Figure 2. Representative microscopy images of primary hippocampal cultures cultivated on different substrates, 14 DIV:

(a) "Control 1"; (b) "Control 2"; (c) culture on hydrogel film; (d) culture on scaffold. Scale bar is 50 jm

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106 CTM J 2018 — v0l. 10, N0.1 T.A. Mishchenko, E.V. Mitroshina, A.I. Kuznetsova, O.M. Shirokova, E.V. Khaydukov, ..., M.V. Vedunova

Figure 3. Representative scanning electron microscopy images of primary hippocampal cultures cultivated on different substrates, 14 DIV:

Vertical columns: (a) "Control 1"; (b) "Control 2"; (c) culture cultivated on scaffolds

Using the method of calcium imaging, functional characteristics of the primary hippocampal cultures cultured on the scaffold were evaluated on 14 DIV. On this day of culture development, we observed the spontaneous calcium activity in the control cultures ("Control 1") (Figure 4). The percentage of cells exhibiting calcium activity was equal to 74.4±15.8%; duration of calcium oscillations was 8.8±0.1 s and the frequency of calcium oscillations per minute was 1.0±0.07. Such level of calcium activity is typical for this period of primary cultures development of medium density [22]. Dissociated hippocampal cultures cultivated on scaffolds also showed functional calcium activity. However, the number of cells exhibited calcium activity (25.2±11.6%) was significantly lower than in the "Control 1" group. Changes in the oscillatory profile manifested in

The main morphometric parameters of primary hippocampal cultures cultivated on different substrates

Groups Feret diameter (Hm) The surface area of single cells (pm2) Surface area of cell conglomerates (pm2)

"Control 1" 13.67±0.36 127.26±3.41 No conglomerates

"Control 2" 11.77±0.44* 74.96i1.89* 33,138.98±4535.89

"Scaffold" 10.84±0.39* 61.53±0.99*# 13,216.04±1253.20#

Note: * versus "Control 1"; # versus "Control 2"; p<0.05, ANOVA, N=4 in each group.

fivefold decrease in the frequency of calcium events (0.2±0.01 osc/min) and in the increase of the duration of calcium oscillations (12.6±1.2 s) are also noted. The decrease in the frequency of calcium events against the background of the increase of calcium oscillations duration suggests the predominant role of glial elements

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attachment of neural and glial cells and contribute to the development of neuronal outgrowth and the formation of network-like structure exhibiting functional metabolic activity.

Thus, scaffolds based on hyaluronic acid glycidyl methacrylate could be considered as a promising material for neurotransplantation.

Conclusion

Scaffolds designed on the basis of hyaluronic acid glycidyl methacrylate have a high biocompatibility with the nervous system cells. Architectonics and adhesive properties of scaffold contribute to the formation of functionally active cell conglomerates.

Financial support. The reported study was funded by RFBR according to the research projects No. 18015-00391, 17-04-01128, 16-04-00245 and Grant of the President of the Russian Federation MD-2634.2017.4. Also, this publication has been prepared as part of the state projects "Provision of scientific research" No.6.6379.2017/8.9, 17.3335.2017/4.6, and 6.6659.2017/6.7. This work was supported by the Federal Agency of Scientific Organizations (Agreement No.007-r3/H3363/26) in the part of synthesis of hydrogel films and scaffolds.

Conflict of interests. The authors declare no conflict of the interests mandatory to be reported.

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110 СТМ J 2018 — vol. 10, No.1 T.A. Mishchenko, RV. Mitroshina, A.I. Kuznetsova, O.M. Shirokova, E.V. Khaydukov, ..., M.V. Vedunova