Publications by authors named "Wei-Juan Shao"

Genome-wide association studies (GWAS) have revealed the implication of several Wnt signaling pathway components, including its effector transcription factor 7-like 2 (TCF7L2) in diabetes and other metabolic disorders. As TCF7L2 is expressed in adipocytes, we investigated its expression and function in rodent fat tissue and mature adipocytes. We found that TCF7L2 mRNA expression in C57BL/6 mouse epididymal fat tissue was up-regulated by feeding but down-regulated by intraperitoneal insulin injection.

View Article and Find Full Text PDF

The study aimed to reveal alterations in expression and methylation levels of the growth-related imprinted genes H19 and Igf2 in fetuses of diabetic mice. Diabetes was induced in female mice by intraperitoneal injection of streptozotocin. DNA and total RNA were extracted from fetuses obtained from diabetic and control dams on embryonic day (E) 14.

View Article and Find Full Text PDF

Insulin promotes early embryonic development, but whether this action affects postimplantation fetal development and alters the expression of imprinted genes remain to be determined. This study analyzed the expression and methylation levels of the growth-related imprinted genes H19 and insulin-like growth factor 2 (Igf2) in fetuses exposed to insulin before implantation. We cultured 2-cell embryos in either 0 or 0.

View Article and Find Full Text PDF

Synopsis of recent research by authors named "Wei-Juan Shao"

  • Wei-Juan Shao's research primarily focuses on the impact of metabolic factors, such as Wnt signaling and insulin exposure, on gene expression in adipocytes and during embryonic development.
  • Findings indicate that activation of the Wnt pathway, particularly TCF7L2, positively regulates leptin gene expression in mature adipocytes, while alterations in insulin influence the expression of imprinted genes related to growth in fetuses exposed during preimplantation.
  • The studies reveal significant implications for understanding metabolic disorders and developmental biology, particularly in the context of diabetes-induced changes in gene expression and epigenetic modifications.