Identification of Goose PKR Gene: Structure, Expression Profiling, and Antiviral Activity Against Newcastle Disease Virus.

Double-stranded RNA-dependent protein kinase (PKR) is an important antiviral IFN-stimulated gene (ISGs) that recognizes double-stranded RNA (dsRNA) and mediates inhibition of translation initiation and protein synthesis in various types of viral infection. In this study, the complete coding sequence (CDS) of goose PKR (goPKR) is identified and characterized. The open reading frame (ORF) of goPKR is 1668 bp, which encodes a polypeptide of 555 amino acids.

[Gossypol decreases the expression of connexin 43 in Sertoli cells].

Objective: To study the effect of gossypol on the expression of connexin 43 (CX43) in Sertoli cells.

Methods: TM4 Sertoli cells were cultured and treated with gossypol at the concentrations of 1.25, 2.

Gap junctional protein connexin 43 in rat detrusor muscle with unstable bladder.

Background: Unstable bladder is one of the common clinical dysfunctions of the lower urinary tract. Gap junctions (GJs) are the plaques of aqueous channels that facilitate electrical and metabolic communication between the intracellular compartments of adjacent cells, exchange of nutrients and ions between connected cells and transfer of electrical signals. In the present study we investigated the quantitative alterations of the GJ in the rat detrusor muscle and its functional changes related to the developing of unstable bladder (USB).

Gossypol repressed the gap junctional intercellular communication between Sertoli cells by decreasing the expression of Connexin43.

Previous studies showed that gossypol could block the gap junctional intercellular communication (GJIC) between cultured cells. The present study was designed to investigate the effects of gossypol on the GJIC and the expression of connexin43 (Cx43) in the cultured cells. A Sertoli cell line, TM4, was treated with different concentrations of gossypol 1.