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1.
Int J Mol Sci ; 21(23)2020 Dec 01.
Article in English | MEDLINE | ID: mdl-33271925

ABSTRACT

In 2020 the world faced the pandemic of COVID-19 severe acute respiratory syndrome caused by a new type of coronavirus named SARS-CoV-2. To stop the spread of the disease, it is crucial to create molecular tools allowing the investigation, diagnoses and treatment of COVID-19. One of such tools are monoclonal antibodies (mAbs). In this study we describe the development of hybridoma cells that can produce mouse mAbs against receptor binding domain of SARS-CoV-2 spike (S) protein. These mAbs are able to specifically detect native and denatured S proteins in all tested applications, including immunoblotting, enzyme-linked immunosorbent assay, immunofluorescence staining of cells and immunohistochemical staining of paraffin embedded patients' tissue samples. In addition, we showed that the obtained mAbs can efficiently block SARS-CoV-2 infection in in vitro experiments. Finally, we determined the amino acid sequence of light and heavy chains of the mAbs. This information will allow the use of corresponding peptides to establish genetically engineered therapeutic antibodies. To date multiple mAbs against SARS-CoV-2 proteins have been established, however, bigger sets of various antibodies will allow the detection and neutralization of SARS-CoV-2, even if the virus acquires novel mutations.


Subject(s)
Antibodies, Monoclonal/metabolism , Antigens, Viral/metabolism , SARS-CoV-2/metabolism , Spike Glycoprotein, Coronavirus/immunology , Amino Acid Sequence , Animals , Antibodies, Monoclonal/chemistry , Antibodies, Monoclonal/immunology , Antigen-Antibody Reactions , Antigens, Viral/immunology , COVID-19/pathology , COVID-19/virology , Enzyme-Linked Immunosorbent Assay , HEK293 Cells , Humans , Hybridomas/cytology , Hybridomas/metabolism , Immunohistochemistry , Lung/pathology , Lung/virology , Mice , Mice, Inbred BALB C , Protein Domains/immunology , Recombinant Proteins/biosynthesis , Recombinant Proteins/immunology , Recombinant Proteins/isolation & purification , SARS-CoV-2/immunology , SARS-CoV-2/isolation & purification , Spike Glycoprotein, Coronavirus/genetics , Spike Glycoprotein, Coronavirus/metabolism
2.
Sci Adv ; 6(29): eaba4174, 2020 07.
Article in English | MEDLINE | ID: mdl-32743068

ABSTRACT

Magnetic levitational bioassembly of three-dimensional (3D) tissue constructs represents a rapidly emerging scaffold- and label-free approach and alternative conceptual advance in tissue engineering. The magnetic bioassembler has been designed, developed, and certified for life space research. To the best of our knowledge, 3D tissue constructs have been biofabricated for the first time in space under microgravity from tissue spheroids consisting of human chondrocytes. Bioassembly and sequential tissue spheroid fusion presented a good agreement with developed predictive mathematical models and computer simulations. Tissue constructs demonstrated good viability and advanced stages of tissue spheroid fusion process. Thus, our data strongly suggest that scaffold-free formative biofabrication using magnetic fields is a feasible alternative to traditional scaffold-based approaches, hinting a new perspective avenue of research that could significantly advance tissue engineering. Magnetic levitational bioassembly in space can also advance space life science and space regenerative medicine.

3.
Biotechnol J ; 15(5): e1900217, 2020 May.
Article in English | MEDLINE | ID: mdl-31995658

ABSTRACT

Reproducible, scalable, and cost effective fabrication and versatile characterization of tissue spheroids (TS) is highly demanded by 3D bioprinting and drug discovery. Consistent geometry, defined mechanical properties, optimal viability, appropriate extracellular matrix/cell organization are required for cell aggregates aimed for application in these fields. A straightforward procedure for fabrication and systematic multiparametric characterization of TS with defined properties and uniform predictable geometry employing non-adhesive technology is suggested. Applying immortalized and primary cells, the reproducibility of spheroid generation, the strong correlation of ultimate spheroid diameter, and growth pattern with cell type and initial seeding concentration are demonstrated. Spheroids viability and mechanical properties are governed by cell derivation. In this study, a new decision procedure to apply for any cell type one starts to work with to prepare and typify TS meeting high quality standards in biofabrication and drug discovery is suggested.


Subject(s)
Biomarkers/metabolism , Spheroids, Cellular/cytology , Tissue Engineering/methods , Animals , Bioprinting , Cell Line , Cell Survival , Fibroblasts/cytology , Fibroblasts/metabolism , HEK293 Cells , Humans , Rats , Spheroids, Cellular/metabolism
4.
Cartilage ; 11(4): 521-531, 2020 10.
Article in English | MEDLINE | ID: mdl-30221989

ABSTRACT

OBJECTIVE: Chondrospheres represent a variant of tissue spheroids biofabricated from chondrocytes. They are already being used in clinical trials for cartilage repair; however, their biomechanical properties have not been systematically investigated yet. The aim of our study was to characterize chondrospheres in long-term in vitro culture conditions for morphometric changes, biomechanical integrity, and their fusion and spreading kinetics. RESULTS: It has been demonstrated that the increase in chondrospheres secant modulus of elasticity is strongly associated with the synthesis and accumulation of extracellular matrix. Additionally, significant interplay has been found between biomechanical properties of tissue spheroids and their fusion kinetics in contrast to their spreading kinetics. CONCLUSIONS: Extracellular matrix is one of the main structural determinants of chondrospheres biomechanical properties during chondrogenic maturation in vitro. The estimation of tissue spheroids' physical behavior in vitro prior to operative treatment can be used to predict and potentially control fusogenic self-assembly process after implantation in vivo.


Subject(s)
Chondrocytes/cytology , Chondrogenesis/physiology , Extracellular Matrix/physiology , Spheroids, Cellular/physiology , Tissue Engineering , Biomechanical Phenomena , Cells, Cultured , Humans , In Vitro Techniques
5.
Exp Eye Res ; 152: 1-9, 2016 11.
Article in English | MEDLINE | ID: mdl-27590659

ABSTRACT

Pigment Epithelium-Derived Factor (PEDF) is a secreted glycoprotein belonging to the family of non-inhibitory serpins. It is known, that in cases of complicated myopia, the content of PEDF in aqueous humor of the anterior chamber is significantly reduced. Here we examined a bulk of Tenon's capsule samples obtained from various groups of myopes, to examine PEDF processing in progressive myopia. We have analyzed the distribution of full length PEDF50 and its truncated form PEDF45 in the soluble and insoluble fractions extracted from Tenon's capsule of myopic and control (non-myopic) patients using SDS-polyacrylamide gel electrophoresis, as well as monitored the proteolytic degradation of PEDF ex vivo by enzyme-linked immunosorbent assay. These results were complemented by PEDF mRNA analysis in correspondent tissues by using qPCR and immunohistochemistry analysis of PEDF distribution in normal and myopic specimens. We found that in the Tenon's capsule of patients suffering from a high myopia the level of "soluble" 45 kDa PEDF reduced by 2-fold, while the content of "insoluble" 50 kDa form of PEDF was increased by 4-fold compared to controls. Excessive amount of PEDF50 in myopic specimens have been shown to correlate with the abrogated PEDF processing rather than with an increase of its expression. Moreover, immunohistochemical staining of the myopic Tenon's capsule tissue sections revealed the halo of deposited PEDF50 in the fibroblast extracellular space. These findings suggest that in myopia limited proteolysis of PEDF is altered or abrogated. Accumulation of full-length PEDF insoluble aggregates in the fibroblast intercellular space may affect cell survival and consequently causes the destructive changes in the extracellular matrix of the eye connective tissues. As a result, the abrogation of full-length PEDF normal processing can be an important mechanism leading to biomechanical destabilization of the scleral capsule and myopia progression.


Subject(s)
Eye Proteins/genetics , Gene Expression Regulation , Myopia, Degenerative/genetics , Nerve Growth Factors/genetics , RNA/genetics , Serpins/genetics , Tenon Capsule/metabolism , Adolescent , Aqueous Humor/metabolism , Blotting, Western , Child , Enzyme-Linked Immunosorbent Assay , Eye Proteins/metabolism , Female , Fibroblasts/metabolism , Fibroblasts/pathology , Humans , Immunohistochemistry , Male , Myopia, Degenerative/diagnosis , Myopia, Degenerative/metabolism , Myopia, Degenerative/physiopathology , Nerve Growth Factors/metabolism , Real-Time Polymerase Chain Reaction , Refraction, Ocular , Serpins/metabolism , Tenon Capsule/pathology , Young Adult
6.
Int J Clin Exp Pathol ; 7(12): 9090-8, 2014.
Article in English | MEDLINE | ID: mdl-25674294

ABSTRACT

An immunohistochemical study on the cells proliferative activity by Ki-67 protein and localization of the matrix metalloproteinase-9 and the inhibitor of matrix metalloproteinase-1 was carried out at the benign prostatic hyperplasia (BPH) and the adenocarcinoma (AC) of different Gleason's grades. A significant decrease of the MMP-9 and TIMP-1 level in the AC of different gradations was observed. A moderate positive correlation between the Gleason score and cell proliferation Ki-67 index (rs = 0.674) and a moderate negative correlation with the level of such a score and expression of MMP-9 (rs = -0.660) was detected. A weak negative correlation exists also between the level of proliferative activity of secretory cells and the expression of MMP-9 by tumor cells (rs = -0.369). The invasive properties of AC cells that promote a degradation of the basal membrane and connective tissue in prostate may be explained by the imbalance between the MMP-9 and TIMP-1, which expression is significantly reduced in AC, in comparison with BPH.


Subject(s)
Adenocarcinoma/enzymology , Biomarkers, Tumor/analysis , Immunohistochemistry , Matrix Metalloproteinase 9/analysis , Prostatic Neoplasms/enzymology , Tissue Inhibitor of Metalloproteinase-1/analysis , Adenocarcinoma/pathology , Aged , Aged, 80 and over , Case-Control Studies , Cell Proliferation , Humans , Ki-67 Antigen , Male , Middle Aged , Neoplasm Grading , Predictive Value of Tests , Prostatic Hyperplasia/enzymology , Prostatic Hyperplasia/pathology , Prostatic Neoplasms/pathology
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