4.6 Article

Mesenchymal stromal cells modulate infection and inflammation in the uterus and mammary gland

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BMC VETERINARY RESEARCH
卷 19, 期 1, 页码 -

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BMC
DOI: 10.1186/s12917-023-03616-1

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Uterus; Metritis; Mastitis; Mesenchymal stromal cells; Murine model; Escherichia coli; Immunomodulation

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The use of mesenchymal stromal cells (MSCs) is a safe and effective treatment for infectious and non-infectious inflammatory diseases in both humans and animals. This study investigated the properties of MSCs and their potential in treating mastitis and metritis, common diseases in dairy cows. The results showed that MSC treatment reduced bacterial load and modulated the inflammatory response in the uterus and mammary gland. This opens new possibilities for the development of MSC-based cell-free therapies.
The use of mesenchymal stromal cells (MSCs) is emerging as an efficacious and safe treatment for many infectious and non-infectious inflammatory diseases in human and veterinary medicine. Such use could be done to treat mastitis and metritis, which are the most common disease conditions affecting dairy cows leading to considerable economic losses and reduced animal welfare. Currently, both disease conditions are commonly treated using local and systemic administration of antibiotics. However, this strategy has many disadvantages including low cure rates and the public health hazards. Looking for alternative approaches, we investigated the properties of MSCs using in-vitro mammary and endometrial cell systems and in-vivo mastitis and metritis murine model systems. In-vitro, co-culture of mammary and uterus epithelial cells constructed with NF-kB reporter system, the master regulator of inflammation, demonstrated their anti-inflammatory effects in response to.LPS. In vivo, we challenge animals with field strains of mammary and utero pathogenic Escherichia coli and evaluated the effects of local and systemic application of MSC in the animal models. Disease outcome was evaluated using histological analysis, bacterial counts and gene expression of inflammatory markers. We show that MSC treatment reduced bacterial load in metritis and significantly modulated the inflammatory response of the uterus and mammary gland to bacterial infection. Most notably are the immune modulatory effects of remotely engrafted intravenous MSCs, which open new avenues to the development of MSC-based cell-free therapies.

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