AIM To investigate the functional role and underlying molecular mechanism of mi R-29 a in hepatitis B virus(HBV) expression and replication.METHODS The levels of mi R-29 a and SMARCE1 in HBV-infected Hep G2.2.15 cells...AIM To investigate the functional role and underlying molecular mechanism of mi R-29 a in hepatitis B virus(HBV) expression and replication.METHODS The levels of mi R-29 a and SMARCE1 in HBV-infected Hep G2.2.15 cells were measured by quantitative real-time PCR and western blot analysis. HBV DNA replication was measured by quantitative PCR and Southern blot analysis. The relative levels of hepatitis B surface antigen and hepatitis B e antigen were detected by enzyme-linked immunosorbent assay. The Cell Counting Kit-8(CCK-8) was used to detect the viability of Hep G2.2.15 cells. The relationship between mi R-29 a and SMARCE1 were identified by target prediction and luciferase reporter analysis.RESULTS mi R-29 a promoted HBV replication and expression, w h i le S MA R C E 1 r e p r e s s e d H B V r e p lic a t io n a n d expression. Cell viability detection indicated that mi R-29 a transfection had no adverse effect on the host cells. Moreover, SMARCE1 was identified and validated to be a functional target of mi R-29 a. Furthermore, restored expression of SMARCE1 could relieve the increased HBV replication and expression caused by mi R-29 a overexpression.CONCLUSION mi R-29 a promotes HBV replication and expression through regulating SMARCE1. As a potential regulator of HBV replication and expression, mi R-29 a could be a promising therapeutic target for patients with HBV infection.展开更多
To observe the morphologic characteristics of spermatozoon ultramicroscopic structure in uremic subjects.Method Semen sample from lO patients with uremia and 5 healthy men were observed under light microscope and scan...To observe the morphologic characteristics of spermatozoon ultramicroscopic structure in uremic subjects.Method Semen sample from lO patients with uremia and 5 healthy men were observed under light microscope and scanning electronic microscope.Results Abnormalities were found in sperms of uremic patients either in the sperm head （acrosome, acrosomic deficit, nuclear abnormality, pointed head, headless and double head of spermatozoon）, neck （rupture, separation and enlargement）, or tail （mitochondrial swelling, mitochondrial deficit, tailless, double tail, short tail and curled tail）; whereas none of the above-mentioned abnormalities was observed in healthy men. Conclusion Sperms of uremic patients had many morphologic and structural abnormalities in the head, neck and tail.展开更多
文摘AIM To investigate the functional role and underlying molecular mechanism of mi R-29 a in hepatitis B virus(HBV) expression and replication.METHODS The levels of mi R-29 a and SMARCE1 in HBV-infected Hep G2.2.15 cells were measured by quantitative real-time PCR and western blot analysis. HBV DNA replication was measured by quantitative PCR and Southern blot analysis. The relative levels of hepatitis B surface antigen and hepatitis B e antigen were detected by enzyme-linked immunosorbent assay. The Cell Counting Kit-8(CCK-8) was used to detect the viability of Hep G2.2.15 cells. The relationship between mi R-29 a and SMARCE1 were identified by target prediction and luciferase reporter analysis.RESULTS mi R-29 a promoted HBV replication and expression, w h i le S MA R C E 1 r e p r e s s e d H B V r e p lic a t io n a n d expression. Cell viability detection indicated that mi R-29 a transfection had no adverse effect on the host cells. Moreover, SMARCE1 was identified and validated to be a functional target of mi R-29 a. Furthermore, restored expression of SMARCE1 could relieve the increased HBV replication and expression caused by mi R-29 a overexpression.CONCLUSION mi R-29 a promotes HBV replication and expression through regulating SMARCE1. As a potential regulator of HBV replication and expression, mi R-29 a could be a promising therapeutic target for patients with HBV infection.
文摘To observe the morphologic characteristics of spermatozoon ultramicroscopic structure in uremic subjects.Method Semen sample from lO patients with uremia and 5 healthy men were observed under light microscope and scanning electronic microscope.Results Abnormalities were found in sperms of uremic patients either in the sperm head （acrosome, acrosomic deficit, nuclear abnormality, pointed head, headless and double head of spermatozoon）, neck （rupture, separation and enlargement）, or tail （mitochondrial swelling, mitochondrial deficit, tailless, double tail, short tail and curled tail）; whereas none of the above-mentioned abnormalities was observed in healthy men. Conclusion Sperms of uremic patients had many morphologic and structural abnormalities in the head, neck and tail.
