Wound healing in crustaceans preserves the integrity of the integument and prevents entry of pathogens. We studied the interaction between the moulting hormones (ecdysteroids) and the cellular events under the wound during wound healing with or without bacteria infection. Wounding of the carapace by abrasion induced a rapid increase in circulating ecdysteroid levels to a low sustained plateau level for about 12 days, followed by a sharp premoult peak and moulting. Within 48h of wounding, the nuclear receptor for ecdysteroids (EcR) appeared in the nuclei of haemocytes (hyaline, semigranular and granulocytes), visualized by confocal laser scanning microscopy and anti-EcR. Hyaline haematocytes aggregated in layers below the wound site and granulocytes engaged in phagocytosis. Therefore, the immune system responds directly and rapidly to ecdysteroids. Epidermal cells developed EcR only several days after the haemocytes and only under intact carapace, not under the wound where they appeared apoptotic. At the wound margin, EcR-positive epidermal cells and fibroblasts proceeded to migrate across the wound between the layers of haemocytes. Epidermis was fully regenerated by day 15; at this time the ecdysteroid titre began rising towards a premoult peak and EcR disappeared from the nuclei of epidermal cells suggesting that high amounts of ecdysteroids exert negative control on EcR. When bacteria were injected at the time of wounding, both the plateau level of ecdysteroid titre and the cellular events of wound healing were prolonged by 5-7 days, showing that healing of the wound is slower and that the duration of the plateau phase of the titre depends on the degree of assault on the animal. We conclude that the low levels of ecdysteroids induced by wounding activate the immune system to begin healing below the wound and also stimulate adjacent epidermal cells to commence the process of wound repair.
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http://dx.doi.org/10.1016/j.ygcen.2007.01.044 | DOI Listing |
Asian Pac J Cancer Prev
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Cancer Chemoprevention Research Center, Faculty of Pharmacy, Universitas Gadjah Mada Sekip Utara II, 55281 Yogyakarta, Indonesia.
Objective: Programmed cell death-1 (PD-1, encoded by PDCD1) regulatory network participates in glioblastoma multiforme development. However, such a network in trastuzumab-resistant human epidermal growth factor receptor 2-positive (HER2+) breast cancer remains to be determined. Accordingly, this study was aimed to explore the PD-1 regulatory network responsible for the resistance of breast cancer cells to trastuzumab through a bioinformatics approach.
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Dermatology and Venereology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.
Vitiligo is a pigmentary disorder acquired and caused by the loss or destruction of melanocytes from the epidermis. There is strong proof that vitiligo is mainly an autoimmune disease. Cathelicidin (LL37), an antimicrobial polypeptide, is an important part of the innate immune system and has a role in different skin autoimmune diseases.
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Division of Cancer Cell Biology, Department of Pharmaceutical Sciences, Showa University Graduate School of Pharmacy, Tokyo, Japan.
The role of the electron transport chain (ETC) in cell proliferation control beyond its crucial function in supporting ATP generation has recently emerged. In this study, we found that, among the four ETC complexes, the complex I (CI)-mediated NAD regeneration is important for cancer cell proliferation. In cancer cells, a decrease in CI activity by RNA interference (RNAi) against NADH:ubiquinone oxidoreductase core subunit V1 (NDUFV1) arrested the cell cycle at the G/S phase, accompanying upregulation of p21 cyclin-dependent kinase inhibitor expression.
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January 2025
Tissue Biology Research Unit, Department of Surgery, University Children's Hospital Zurich, Lenggstrasse 30, Zurich, 8008, Switzerland.
The bioengineering of vascular networks is pivotal to create complex tissues and organs for regenerative medicine applications. However, bioengineered tissues comprising an arterial and venous plexus alongside a lymphatic capillary network have not been explored yet. Here, scRNA-seq is first employed to investigate the arterio-venous endothelial cell marker patterning in human fetal and juvenile skin.
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Graduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Ferroptosis has been characterised by disruption of the cell membrane through iron-related lipid peroxidation. However, regulation of iron homeostasis in lung cancer cells that are resistant to epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) remains unclear. Transcriptome analysis identified a significant downregulation of apoptosis-associated tyrosine kinase (AATK) mRNA expression in gefitinib-resistant PC9 (PC9-GR) cells, which were found to be more susceptible to ferroptosis inducers.
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