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Published on: January 22, 2019
Effects of SCR-3 on the immunosuppression accompanied with the systemic inflammatory response syndrome
1Department of Anesthesia, General Hospital of Chengdu Military Command Area, Chengdu 610083, Sichuan Province, People's Republic of China.
Abstract:
Steroid receptor coactivator-3 (SRC-3) is a multifunctional protein that plays an important role in mammary gland growth, development, and tumorigenesis. In this study, SCR-3 gene knockout mice were used to study the effects of SCR-3 on the immunosuppression accompanied with systemic inflammatory response syndrome (SIRS). Bacterial clearance assay was performed by blood culture and frozen sections, and the results showed that the absence of SCR-3 protein serious damaged the innate immune system and the body's ability to inactivate or phagocytosis of bacteria was significantly decreased, and the absence of SCR-3 protein also weakened phagocytes' ability to degrade bacteria and their metabolites. Furthermore, animal model of inflammatory reaction was established and the immune function was determined, and the results revealed that SRC-3 protein may play an important role in maintenance of T-cells' immune function, and severe T-cell immune function disorder would be resulted once SRC-3 protein is missing. In addition, the results of our study showed the steady-state of lymphocyte subsets was destroyed after SIRS, leading the suppression of cellular immune function, and the absence of SCR-3 protein may aggravate the suppression of T-lymphocyte function. Therefore, the present study demonstrated that the absence of SCR-3 protein would aggravate immunosuppression. In addition, SRC-3 protein is a significant regulator of infection and inflammation, and SRC-3 protein play an essential role in the development of immunosuppression accompanied with SIRS.
Insights
Steroid receptor coactivator-3 (SRC-3) deficiency severely impairs the innate immune system, hindering bacterial clearance. Absence of SRC-3 exacerbates immunosuppression during systemic inflammatory response syndrome (SIRS).
Area of Science:
- Immunology
- Molecular Biology
- Cellular Biology
Background:
- Steroid receptor coactivator-3 (SRC-3) is a key protein in mammary gland development and tumorigenesis.
- Systemic inflammatory response syndrome (SIRS) is often accompanied by immunosuppression.
- The role of SRC-3 in immune response during SIRS is not well understood.
Purpose of the Study:
- To investigate the role of SRC-3 in the innate immune response during SIRS.
- To determine the effect of SRC-3 deficiency on bacterial clearance and immune cell function.
Main Methods:
- Utilized SRC-3 gene knockout mice.
- Performed bacterial clearance assays using blood cultures and frozen sections.
- Established an animal model of inflammatory reaction to assess immune function.
- Analyzed lymphocyte subsets and T-cell immune function.
Main Results:
- Absence of SRC-3 significantly damaged the innate immune system, decreasing bacterial inactivation and phagocytosis.
- SRC-3 deficiency weakened phagocytes' ability to degrade bacteria and their metabolites.
- SRC-3 plays a crucial role in maintaining T-cell immune function; its absence leads to severe T-cell immune disorder.
- SIRS destroyed lymphocyte subset homeostasis, suppressing cellular immunity, an effect aggravated by SRC-3 absence.
Conclusions:
- SRC-3 deficiency exacerbates immunosuppression during SIRS.
- SRC-3 is a critical regulator of infection and inflammation.
- SRC-3 protein is essential for the development of immunosuppression associated with SIRS.
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