The maintenance effect of β-amyloid injection in the CA1 region of hippocampus on learning and spatial memory in adult male rats

Background: Alzheimer’s disease is one of the most common neurodegenerative diseases that lead to the progressive loss of mental, behavioral and learning abilities. The aim of this study was to investigate the maintenance effect of β-amyloid1-42 (Aβ) injection in the CA1 region of hippocampus on learning and spatial memory of adult male rats using the Morris water maze test. Materials and Methods: In this study, 42 adult male Wistar rats were randomly divided into control (intact), sham (Aβ solvent) and Aβ-injected groups (5 μg/μl). The β-amyloid and its solvent were bilaterally injected into the CA1 region of rats' hippocampus. The first recipient group of Aβ and its solvent after 6, the second group after 11 and the third groups after 31 days were trained by the Morris water maze test. Results: During 4 training days and also in probe and visible tests, there was no significant difference between control and sham groups. The results of the learning steps in Aβ groups showed that traveled distance and escape latency to find the hidden platform was significantly increased compared with the sham groups, but there was no significant difference in the probe and visible tests between these groups. Conclusion: It seems that long exposure to Aβ can lead to more memory and learning loss in animals with Alzheimer

The progress and research trends in oncolytic virotherapy: The bibliometric analysis from 2000 to 2019

Introduction: The objective of the present report is to perform the first comprehensive bibliometric analysis of oncolytic virotherapy research publications. Methods: Scopus was employed as a major database. The total number of publications was found to be 4369, majorly comprising of research articles (n=2895) and reviews (1082). The ANOVA F-test and Welch F-tests were performed to determine the significance (P=0.05). Results: In all publications (3751), the total numbers of authors were 11418 and 10480 different organizations, departments or institutes. We specifically selected seven different viral strains and provided details about the co-authorship network. We also provided details about the top 10 most cited documents. Conclusion: This may provide a quantitative overview about the trends and publications in oncolytic virotherapy research

Fiber manipulation and post-assembly nanobody conjugation for adenoviral vector retargeting through SpyTag-SpyCatcher protein ligation

For adenoviruses (Ads) to be optimally effective in cancer theranostics, they need to be retargeted toward target cells and lose their natural tropism. Typically, this is accomplished by either engineering fiber proteins and/or employing bispecific adapters, capable of bonding Ad fibers and tumor antigen receptors. This study aimed to present a simple and versatile method for generating Ad-based bionanoparticles specific to target cells, using the SpyTag-SpyCatcher system. The SpyTag peptide was inserted into the HI loop of fiber-knob protein, which could act as a covalent anchoring site for a targeting moiety fused to a truncated SpyCatcher (SpyCatcherΔ) pair. After confirming the presence and functionality of SpyTag on the Ad type-5 (Ad5) fiber knob, an adapter molecule, comprising of SpyCatcherΔ fused to an anti-vascular endothelial growth factor receptor 2 (VEGFR2) nanobody, was recombinantly expressed in Escherichia coli and purified before conjugation to fiber-modified Ad5 (fmAd5). After evaluating fmAd5 detargeting from its primary coxsackie and adenovirus receptor (CAR), the nanobody-decorated fmAd5 could be efficiently retargeted to VEGFR2-expressing 293/KDR and human umbilical vein endothelial (HUVEC) cell lines. In conclusion, a plug-and-play platform was described in this study for detargeting and retargeting Ad5 through the SpyTag-SpyCatcher system, which could be potentially applied to generate tailored bionanoparticles for a broad range of specific targets; therefore, it can be introduced as a promising approach in cancer nanotheranostics

Activating Natural Killer Cell Receptors, Selectins, and Inhibitory Siglecs Recognize Ebolavirus Glycoprotein

Expression of the extensively glycosylated Ebolavirus glycoprotein (EBOV-GP) induces physical alterations of surface molecules and plays a crucial role in viral pathogenicity. Here we investigate the interactions of EBOV-GP with host surface molecules using purified EBOV-GP, EBOV-GP-transfected cell lines, and EBOV-GP-pseudotyped lentiviral particles. Subsequently, we wanted to examine which receptors are involved in this recognition by binding studies to cells transfected with the EBOV-GP as well as to recombinant soluble EBOV-GP. As the viral components can also bind to inhibitory receptors of immune cells (e.g., Siglecs, TIM-1), they can even suppress the activity of immune effector cells. Our data show that natural killer (NK) cell receptors NKp44 and NKp46, selectins (CD62E/P/L), the host factors DC-SIGNR/DC-SIGN, and inhibitory Siglecs function as receptors for EBOV-GP. Our results show also moderate to strong avidity of homing receptors (P-, L-, and E-selectin) and DC-SIGNR/DC-SIGN to purified EBOV-GP, to cells transfected with EBOV-GP, as well as to the envelope of a pseudotyped lentiviral vector carrying the EBOV-GP. The concomitant activation and inhibition of the immune system exemplifies the evolutionary antagonism between the immune system and pathogens. Altogether these interactions with activating and inhibitory receptors result in a reduced NK cell-mediated lysis of EBOV-GP-expressing cells. Modulation of these interactions may provide new strategies for treating infections caused by this virus.publishedVersio

Cell 'vision': complementary factor of protein corona in nanotoxicology

peer reviewe

A novel medium-throughput biological assay system for HTLV-1 infectivity and drug discovery

Objective(s): Here, a reporter cell line containing two reporter vectors were developed, in order to monitor the Human T-Lymphotropic Virus type1(HTLV-1) infectivity and the cell viability simultaneously. Materials and Methods: The reporter cell line was constructed by stably transfected baby hamster's kidney cell line (BHK-21), with the genomes expressing two different reporters in separate plasmids.The first reporter gene is transactivated by the HTLV-1 tax protein, while the second reporter is continuously expressed when introduced into a mammalian cell. In order to show its functionality, the effect of the drug mix on HTLV-1 was assayed by this system and was compared to the results obtained by other methods. Results: HTLV-1 reporter cell line was found to produce high level of luciferase when co-cultured with MT-2 and Hut-102 cells but not with Jurkat cell. Moreover, the combination therapy against HTLV-1 can reduce luciferase expression of the cell when co-cultured with MT-2 and Hut-102 comparable to the ELISA (R=0.932, P-value =0.002). In addition, the results revealed the superiority of the present system over the molecular methods. Conclusion: The results demonstrated that the biological assay system is a beneficial tool for the medium-throughput anti-HTLV-1 drug screening and inhibitory effect

Effect of Nanoparticles on cell-life cycle

peer reviewe

The maintenance effect of β-amyloid injection in the CA1 region of hippocampus on learning and spatial memory in adult male rats

Background: Alzheimer’s disease is one of the most common neurodegenerative diseases that lead to the progressive loss of mental, behavioral and learning abilities. The aim of this study was to investigate the maintenance effect of β-amyloid1-42 (Aβ) injection in the CA1 region of hippocampus on learning and spatial memory of adult male rats using the Morris water maze test. Materials and Methods: In this study, 42 adult male Wistar rats were randomly divided into control (intact), sham (Aβ solvent) and Aβ-injected groups (5 μg/μl). The β-amyloid and its solvent were bilaterally injected into the CA1 region of rats' hippocampus. The first recipient group of Aβ and its solvent after 6, the second group after 11 and the third groups after 31 days were trained by the Morris water maze test. Results: During 4 training days and also in probe and visible tests, there was no significant difference between control and sham groups. The results of the learning steps in Aβ groups showed that traveled distance and escape latency to find the hidden platform was significantly increased compared with the sham groups, but there was no significant difference in the probe and visible tests between these groups. Conclusion: It seems that long exposure to Aβ can lead to more memory and learning loss in animals with Alzheimer