Constitutive apoptosis in equine peripheral blood neutrophils in vitro.
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
The researchers conducted this study to gain a deeper understanding of apoptosis (programmed cell death) in equine (horse) peripheral blood neutrophils (a type of white blood cell) and how various factors might change the rate of this process. They discovered that these neutrophils undergo spontaneous apoptosis when left in culture for up to 36 hours, which showed similar characteristics to apoptosis observed in various other cells, including human neutrophils. They also found that certain agents had an impact on equine neutrophil apoptosis rates.
Detailed Assessment of Constitutive Apoptosis
- Neutrophils, a type of essential white blood cell in horses, were identified to undergo time-dependent constitutive apoptosis, a natural cell death process vital for the body to replace old cells with new ones, when cultured for up to 36 hours.
- This spontaneous cell death was found similar to apoptosis in other cells, including human neutrophils, indicating that the apoptosis processes in these horse white blood cells have common features and mechanisms with other cell types.
The Role of ZAS and PMA
- The researchers noted that neutrophils under apoptosis showed diminished responses to ZAS-stimulated chemiluminescence, a measure of the neutrophils’ activity, suggesting that apoptotic cells are less energetically active.
- However, these cells maintained their responsiveness to PMA, a potent activator of cells, indicating that even in an apoptotic state, these neutrophils could still be activated.
Impact of Other Agents on Equine Neutrophil Apoptosis
- LPS, tumor necrosis factor α, and phagocytosis of opsonised ovine erythrocytes were all found to promote equine neutrophil apoptosis, showing that these elements can stimulate the cell death process.
- Contrarily, the introduction of dexamethasone and ZAS showed an inhibitive effect on apoptosis, showing that these agents could potentially slow down the natural cell death processes.
- Interestingly, several agents such as formyl-Met-Leu-Phe, leukotriene B4, platelet activating factor, and PMA, which commonly affect other cells, found no significant effect on equine neutrophil apoptosis.
- These findings signify areas of differentiation between human and horse neutrophils, in terms of their response to LPS and the time-dependent response to dexamethasone.
In summary, this study deepens our understanding of immune cell function in horses and the mechanisms that underlie white blood cell lifespan, which have implications for equine health and disease.
Cite This Article
Publication
Researcher Affiliations
- Royal (Dick) School of Veterinary Studies and the Roslin Institute, University of Edinburgh, Roslin, Midlothian EH25 9RG, UK.
- Royal (Dick) School of Veterinary Studies and the Roslin Institute, University of Edinburgh, Roslin, Midlothian EH25 9RG, UK.
- Queen's Medical Research Institute (QMRI), Medical School, University of Edinburgh, Edinburgh EH16 4TJ, UK.
- Rayne Laboratory, Medical School, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.
- Royal (Dick) School of Veterinary Studies and the Roslin Institute, University of Edinburgh, Roslin, Midlothian EH25 9RG, UK. Electronic address: bruce.mcgorum@ed.ac.uk.
MeSH Terms
- Animals
- Apoptosis
- Cells, Cultured
- Horses
- Neutrophils / physiology
Grant Funding
- G0901697 / Medical Research Council
- MR/J014702/1 / Medical Research Council
- Wellcome Trust
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Citations
This article has been cited 3 times.- Degroote RL, Weigand M, Hauck SM, Deeg CA. IL8 and PMA Trigger the Regulation of Different Biological Processes in Granulocyte Activation.. Front Immunol 2019;10:3064.
- Otrocka-Domagała I, Paździor-Czapula K, Gesek M. Dexamethasone-induced impairment of post-injury skeletal muscle regeneration.. BMC Vet Res 2019 Feb 11;15(1):56.
- Herteman N, Vargas A, Lavoie JP. Characterization of Circulating Low-Density Neutrophils Intrinsic Properties in Healthy and Asthmatic Horses.. Sci Rep 2017 Aug 10;7(1):7743.