Journal
INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 96, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.intimp.2021.107772
Keywords
Malnutrition; Tooth extracted wound; Inflammation; HMGB1; IL-1 beta; Wound healing
Categories
Funding
- China Scholarship Council [201708050140]
- JSPS KAKENHI [JP 19 K10128]
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Malnutrition leads to delayed wound healing by potentially interfering with the HMGB1-IL-1 beta inflammatory response cascade. This study observed changes in related factors in a malnutrition mouse model and identified the mechanism of delayed wound healing.
Malnutrition causes prolonged inflammation, resulting in delayed wound healing. High mobility group box-1 (HMGB1) is a damage-associated molecular pattern that is present in the nuclei of macrophages and is secreted into the extracellular milieu in response to stimuli. It stimulates the production of interleukin-1 beta (IL-1 beta) through the receptors for advanced glycation end products (RAGE), inducing an inflammatory response, which is an essential response to initiate wound healing. We hypothesized that malnutrition may interfere with this cascade, causing abnormal inflammation and ultimately delaying wound healing. We used tooth-extracted mice with malnutrition fed with low-casein diet for two weeks. On days 3 and 7 after tooth extraction, the wound tissue was histologically observed and analyzed for several factors in the inflammation-regeneration lineage, including IL-1 beta mesenchymal stem cells, myeloperoxidase activity, HMGB1, macrophage polarization, and adenosine 5-triphosphate (ATP). On day 7, delayed wound healing was observed with the following findings under malnutrition conditions: decreased mRNA expression of genes for regeneration and mesenchymal stem cell (MSC) accumulation, an obvious increase in myeloperoxidase and IL-1 beta mRNA expression, an increase in HMGB1 levels, and an increase in ATP concentration in tissues with elevated proportion of M2 macrophages. These results suggest that the significantly increased secretion of HMGB1 associated with the upregulated production of ATP and IL-1 beta secretion via the RAGE pathway may interfere with the resolution of inflammation and wound healing under the state of malnutrition.
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