Feeling low: How social media influences employees' knowledge hidings and innovative behavior.

Prior research has identified both positive and negative consequences arising from the widespread integration of social media within the organizations. The present research suggests that upward social comparison (USC) in social media is related to psychological disengagement resulting in knowledge hiding and lower innovative behavior of individuals. It further suggests that mindfulness mitigates the impact of USC in social media. A two-wave longitudinal survey reveals that individuals who engage in comparative self-assessment with friends projecting an aura of unattainable success on social media unwittingly cause psychological disengagement, a phenomenon which, in turn, precipitates a palpable decline in their innovative behavior and rise in knowledge hiding. Furthermore, our exploration unravels an intricate layer of this narrative - mindfulness of employees for online social interactions reduces this adverse cascade. This study draws attention to the necessity for vigilant managerial oversight. It serves as a clarion call, illuminating the concealed facets of social media, dappled with the intricate interplay of online social comparisons. This research transcends traditional paradigms by introducing a unique perspective on employee engagement with social media, contemplated in the context of online social comparison. It augments the current body of knowledge by shedding light on the complex interplay of these variables within the modern workforce.

KISS-1 knockdown inhibits cell growth, migration, and invasion in HTR-8/SVneo cells by regulating the GRP54-mediated PI3K/AKT signaling pathway.

Recurrent spontaneous abortions (RSA) affect reproductive health and increase the risk of subsequent abortions. To investigate the role of KISS-1/GPR-54 signaling in RSA progression. Villus tissue was collected from RSA patients, and human trophoblastic HTR-8/SVneo cells were used. KISS-1 and GRP54 levels were detected using RT-qPCR and immunohistochemistry. Western blotting was performed to analyze ZO-1 and ZEB1 levels. Cell proliferation was determined via CCK-8 and cell clone formation assays. Transwell assays were performed to assess cell migration and invasion abilities. KISS-1 was down-regulated in the villus tissues of RSA patients. KISS-1 overexpression dramatically inhibited trophoblast proliferation, migration, and invasion. Mechanistically, ZEB1 expression was down-regulated, whereas ZO-1 expression was up-regulated, after KISS-1 overexpression. GPR54 silencing neutralized the effect of KISS-1 in HTR-8/SVneo cells. Additionally, KISS-1 overexpression inactivated the PI3K/AKT signaling pathway through GRP54. The KISS-1/GPR-54 signaling axis regulates RSA progression by regulating the PI3K/AKT signaling pathway.

[Analysis of genetic diversity and biological functional site of HIV-1 gp120 from a patient with AIDS dementia complex].

To explore the relationship between the genetic diversity and biological functional site of human immunodeficiency virus HIV-1 gp120 and the pathogenesis of AIDS dementia complex (ADC), the full length sequences of gp120 gene was amplified with PCR from genomic DNA which was extracted from lymphoid and different brain department (periaortic lymphoid, temporal gray/white matter junction, periventricular tissue, choroids plexus, occipital white matter and occipital gray/white matter junction.) of a patient who died of ADC. PCR products were cloned into the pGEM-T vector and positive clones were sequenced. The analysis of neighbor-joining tree, N-glycosylation sites, values of ds/dn, and loop were then all performed. The samples were all identified as HIV-1 B and genetic variation existed in HIV-1 gp120 isolated from different tissues. Compared with standard HIV-1B gp120, biological functional sites of HIV-1 gp120 isolated from the patient changed to some extent. In addition, there were differences in some biological functional sites of HIV-1 gp120 between lymphoid and brain. Therefore, genetic diversity and alterations of some biological functional sites of HIV-1 gp120 might be associated with the pathogenesis of ADC.

Amino acid substitutions in leucine zipper motif in the F-specific domain of human parainfluenza virus 3 HN protein play important roles in the protein function.

OBJECTIVES: To explore the effects of leucine zipper motif in F-specificity domain of human parainfluenza virus 3 (hPIV3) HN protein on the membrane fusion promotion activity. METHODS: Site-directed mutagenesis was performed to generate mutants in leucine zipper motif of hPIV3 HN protein. Combined mutants were obtained from individual mutants. Each mutant was co-expressed with the wild-type (wt) hPIV3 F gene in eukaryotes, using the vaccinia-T7 RNA polymerase expression system. Cell fusion functions were assayed with Giemsa staining and reporter gene method. The expression of HN protein on cell surface was analyzed with fluorescence-activated cell sorter (FACS). Hemadsorption assay was performed to determine the receptor-binding activity of HN mutants. RESULTS: The conserved amino acids in the F-specificity domain of the hPIV3 HN protein were mutated and 9 single mutants were obtained. Based on the single mutants, 2 combined mutants were obtained. Compared to the wt HN protein, the membrane fusion promotion activity of each mutant HN protein was, to some extent, decreased. Among these single mutants, I125A showed the lowest fusion promotion activity, with 34.8% of fusion promotion activity compared to wt HN. In contrast, the fusion promotion activity of I128A was the highest, showing 90.9% of wt HN. In combined mutations, no cell fusion was observed, suggesting fusion promotion activity was negligible. All mutants had a limited effect on receptor-binding activity, and I125A showed the lowest activity, with 85.86% of wt HN. FACS analysis indicated that all mutants were expressed on the cell surface. CONCLUSIONS: Leucine zipper motif in the F-specificity domain had an important effect on the fusion promotion ability of hPIV3 HN protein. A mutation in the motif will diminish or abolish the fusion promotion activity of hPIV3 HN protein. A complete leucine zipper motif was prerequisite to the fusion promotion of HN protein.

[Cloning and sequence analysis of envelope glycoprotein G2 gene of hantavirus in Shandong province].

OBJECTIVE: To construct the cloning vector of glycoprotein G2 gene of hantavirus (HV), to analyze the sequence of G2 gene by the phylogenetic tree, and to study the differences among glycoprotein G2 genes from the world around. METHODS: Envelope glycoprotein G2 gene was amplified from four specimens of Shandong province by RT-PCR, and the product recombined into the PMD-18T vector. The clones that carry the G2 gene were identified. After sequencing, the gene sequence was handled with the software DNASTAR, compared with 24 strains worldwide and the phylogenetic tree was drawn. RESULTS: HV G2 gene was amplified by RT-PCR from 4 specimens, named GM04-38.G2, ZB8.G2, JUN5-14.G2, RCH5.G2, respectively. The map of the phylogenetic tree showed that all the 4 strains belonged to SEO-type hantavirus. The analysis of the sequence showed that all the four HV strains had the highest rates of homology with Z37 strain. The sequence homology of SEO-type HV strains was from 82.3% to 99.8%. CONCLUSION: The four cloning vectors containing the glycoprotein G2 genes were successfully constructed. Envelope glycoprotein G2 gene of four specimens from Shandong province had high homology rates.

Genetic properties of medium (M) and small (S) genomic RNA segments of Seoul hantavirus isolated from Rattus norvegicus and antigenicity analysis of recombinant nucleocapsid protein.

A novel isolate of Seoul (SEO) hantaviruses was detected and identified in Rattus norvegicus in Shandong Province, China and designated as JUN5-14. The partial M segment and the coding region of nucleocapsid protein (NP) in the S segment of JUN5-14 were PCR-amplified and sequenced. Nucleotide sequence analysis of the partial M segment (300 bp) revealed that JUN5-14 isolate was closely related to former SEO isolates in Shandong (97.3-99.0% homology) and non-Shandong SEO viruses (84.1-97.7% homology) but distantly related to other hantaviruses (61.5-75.1% homology). Consistent with the M segment, the coding region of the NP showed 87.5-97.8% and 97.9-99.8% identity with SEO viruses and 55.2-75.8% and 47.2-84.4% homology with other hantaviruses, at nucleotide and amino acid level, respectively. The virus isolate was identified as a member of the subtype 3 (S3) of SEO viruses by phylogenetic trees generated from the nucleotide sequences of the S and M segments. In order to develop a diagnostic assay for hantavirus infection in human, the full-length NP gene of JUN5-14 was expressed in BHK21 cells using the T7 RNA polymerase expression system. The NP expression was confirmed by indirect immunofluorescence assay (IFA) and Western blotting. The expressed NP protein was used as antigen to detect antibody response against NP in patients with hemorrhagic fever with renal syndrome (HFRS) in an IgG-IFA. Sixteen out of seventeen serum samples showed positive for the presence of anti-NP antibodies, indicating that the recombinant NP (rNP) protein of JUN5-14 was a good antigen for detecting hantavirus infection in human.

Effects of heptad repeat regions of f protein on the specific membrane fusion in paramyxoviruses.

OBJECTIVES: To identify the effects of heptad repeat regions (HR1 and HR2) of F on the specific membrane fusion in paramyxoviruses. METHODS: Site-directed mutagenesis was used to create same enzyme sites on the F genes of Newcastle disease virus (NDV) and human parainfluenza virus (hPIV). Gene recombination was used to get chimeric F proteins NDV C-HR1 and hPIV C-HR1 by exchanging HR1 fragments each other; NDV C-HR2 and hPIV C-HR2 were also obtained by the same way. All the chimeric F proteins were co-expressed with their homologous or heterogeneous HN in eukaryocytes. Cell fusion functions were assayed by Giemsa staining and reporter gene method. The expression efficiencies of F proteins were assayed with fluorescence-activated cell sorter (FACS). RESULTS: NDV C-HR1 and hPIV C-HR1 had 53.91 and 83.15% of fusion activities, and NDV C-HR2 and hPIV C-HR2 had 107.23 and 12.01% of fusion activities, respectively, as compared with their relevant wild types. The analysis of FACS indicated that the expression efficiencies of all the chimeric F proteins except NDV C-HR2 were lower than those of their relevant wild types. CONCLUSIONS: HR1 of NDV F might be important for its specific membrane fusion, but HR2 of NDV F may not; both HR1 and HR2 of hPIV F may be important for its specific membrane fusion.

[Studies on anti-HSV effect of Ficus carica leaves].

OBJECTIVE: To study the anti-HSV effect of the extract from the leaves of Ficos carica. METHODS: The effective ingredient was extracted from the leaves of Ficus carica, and the anti-virus effect was observed on Hep-2, BHK21 and PRK cells. RESULTS: The water extract from the leaves of Ficus carica possessed distinct anti-HSV-1 effect. The MTC was 0.5 mg/ml, TDO was 15 mg/ml, and TI was 30.0. It possessed low toxicity and directly killing-virus effect on HSV-1. CONCLUSIONS: The leaves of Ficus carica possess anti-HSV-1 effect, and their application on the area of medicine, food and drugs has expansive foreground.

[Inhibition effects of rhubarb ethanol extract on herpes simplex virus infection in vivo].

OBJECTIVE: To know the anti-viral effects of rhubarb ethanol extract (REE) on herpes simplex virus(HSV) infection in vivo. METHODS: BALB/c mice inoculated from tail vein with 0.15 ml of HSV (TCID50=10(3)) were injected hypodermically with REE next day. After divided into seven groups, three groups of mice were given different doses of REE respectively and the other groups as controls. Pathological sections from the liver, spleen, kidney were made at different times of postinfection, and their pathological changes were observed under microscope; the virus titers in viscera were assayed by using plaque formation technique and the rhubarb inhibitions to the infection of HSV in vivo?were observed. RESULTS: No toxic response to mice were observed for REE injected hypodermically; no pathological changes were observed in different therapy groups of spleens. And those in livers and kidneys at medium- and high-dosed groups disappeared quickly. The effect of low-dosed group was equal to that of positive control group, acyclovir(ACV); the results of the titer tests showed that the virus decreased rapidly by using REE, especially in the medium- and high-dosed groups which were much more marked than the low-dosed group; Q test of the data showed that total mean value had statistical significance (F=49.1459, P<0.01); moreover there were statistical significance between therapy groups (ACV, DH1, DH2, DH3) and non-therapy groups (VC) (P<0.01 ) and between DH2, DH3 and DH1 (P<0.01); no statistical significance were found between DH1, DH2 or DH3 and ACV (P>0.05). Results show that as to the effect of decreasing the average of the total titer, rhubarb is as effective as ACV; furthermore, the medium- and high-dosed groups are superior to the low-dosed group. CONCLUSIONS: REE has significant anti-viral effect on HSV in vivo; there will be a wide application foreground of it in clinical usage.

Characteristics and mechanisms of isolated rubella virus, strain JR23: infection of the central nervous system of BALB/c mice.

OBJECTIVE: To investigate the correlation between rubella virus (RuV) antigen in peripheral lymphocytes, the immune status and RuV infection in the central nervous system (CNS). METHODS: BALB/c mice were used as a model and treated with immunoaffecting medicines. Then, the mice were infected with RuV via the abdominal cavity, and the antigen level in peripheral lymphocytes was examined 1, 3, 7 and 14 days postinfection. RuV in the CNS was detected by immunohistochemical methods. BALB/c mice were given dexamethasone and cytoxan before infection with the RuV JR23 strain. Immune functions and RuV invasion of the CNS were assayed on day 21 postinfection via the abdominal cavity, and their relationship was analyzed. RESULTS: The mean antigen detection rates at different times were 3.1, 4.1, 9.6 and 2.4%, respectively, in the dexamethasone group, and 14.2, 12.7, 9.9 and 3.1%, respectively, in the cytoxan group. In the group without any intervention, the detection rates were 4.63, 10.25, 6.88 and 1.75%, respectively. The antigen detection rates in peripheral lymphocytes among the three groups 24 h postinfection were significantly different (F = 0.0317, p < 0.05). Comparisons between groups showed that antigen detection rates in the cytoxan group were much higher than those in other groups, but there was no difference between the dexamethasone and control groups. The animals with persistent presence of antigen were much more susceptible to cerebral infection than those with short-term presence (p < 0.001). T cell functions of the cytoxan group were significantly lower than those of other groups (p < 0.05), as detected by the MTT method. Infection rates of the dexamethasone, cytoxan and control groups were 60, 90 and 50%, respectively. Cell immune functions of the mice with CNS infection were obviously worse than those of the mice without CNS infection (p < 0.001). RuV-specific antibodies were assayed in all groups by ELISA and the results showed that there were no significant differences among groups (p < 0.05) or between the groups with and without CNS infection. CONCLUSION: Cytoxan can affect virus detection rates in peripheral lymphocytes. At the early phase of infection, the persistent presence of RuV in peripheral lymphocytes increases the incidence of CNS infection. RuV infection in the CNS was related to the cell immune situation before specific antibody was produced in the body.

[Immune status of BALB/c mice and rubella virus JR23 strain infection of central nervous system].

BACKGROUND: To investigate the relationship between immune status and rubella virus (RV) infection of central nervous system (CNS). METHODS: BALB/c mice were given dexamethaxone and cytoxan before RV JR23 strain infection. Immune functions and RV invasion to CNS were assayed at 21 days postinfection via abdominal cavity and their relationship was analyzed. RESULTS: T cell functions of cytoxan group were obviously worse than those of other groups (P <0.05) by MTT method. Infection rates of dexamethaxone and cytoxan and the group without any intervention were 60%, 90% and 50% (P >0.05), respectively. Cellular immune functions of the mice with CNS infection were obviously worse than those of the mice without CNS infection (P <0.001). Specific antibodies (Ab) were assayed in all groups with ELISA and the results showed that there were no significant differences among groups (P >0.05), neither between the groups with and without CNS infections. CONCLUSIONS: RV infection of CNS may relate to cellular immune status before specific antibody was produced in the body.