Difference between revisions of "Neutrophils"
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This is the process of granule fusion with the plasma membrane, causing the release of the granule contents into the immediate vicinity. Contents can include vasoactive peptides, for example, histamine and bradykinin which, as their name suggests, activate the endothelium. This causes the endothelium to become more "leaky" causing a great increase in extravasation of blood granulocytes and monocytes, and the diffusion of plasma proteins to the site of infection. These peptides, released from other cells as well as neutrophils (e.g. [[Mast cells|Mast cells]], are responsible for the classical signs of inflammation: redness (rubor), heat (calor), swelling (tumor), and pain (dolor), often accompanied by loss of function. | This is the process of granule fusion with the plasma membrane, causing the release of the granule contents into the immediate vicinity. Contents can include vasoactive peptides, for example, histamine and bradykinin which, as their name suggests, activate the endothelium. This causes the endothelium to become more "leaky" causing a great increase in extravasation of blood granulocytes and monocytes, and the diffusion of plasma proteins to the site of infection. These peptides, released from other cells as well as neutrophils (e.g. [[Mast cells|Mast cells]], are responsible for the classical signs of inflammation: redness (rubor), heat (calor), swelling (tumor), and pain (dolor), often accompanied by loss of function. | ||
| − | ===Further amplification of inflammation=== | + | ====Further amplification of inflammation==== |
| − | Neutrophils have many mechanisms to increase inflammation. These include [[Cytokines|cytokine]] release and exocytosis of vasoactive peptides as mentioned above. Neutrophil activation in an inflammatory lesion can also result in the release of prostaglandins, through synthesis by cyclo-oxygenase 2, which are responsible for vasoactive changes and for pain (N.B. These are reduced with cyclo-oxygenase (COX) inhibition for example with the NSAID (non-steriodal anti-inflammatory drugs)'s Aspirin and Ibuprofen). | + | Neutrophils have many mechanisms to increase inflammation. These include [[Cytokines|cytokine]] release and exocytosis of vasoactive peptides as mentioned above. Neutrophil activation in an inflammatory lesion can also result in the release of prostaglandins, through synthesis by cyclo-oxygenase 2, which are responsible for vasoactive changes and for pain (N.B. These are reduced with cyclo-oxygenase (COX) inhibition for example with the NSAID (non-steriodal anti-inflammatory drugs)'s Aspirin and Ibuprofen). |
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===Interactions=== | ===Interactions=== | ||
<p>Il-6, Il-8 and C5a are all chemoattractants for neutrophils.</p> | <p>Il-6, Il-8 and C5a are all chemoattractants for neutrophils.</p> | ||
Revision as of 10:14, 2 May 2012
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Introduction
Neutrophils represent up to 70% of all leukocytes in the blood stream and are distinguished by their irregular multi-lobed nucleus and indistinct granular appearance. They are 10-12µm and circulate in the blood for minutes to hours (average 6-8 hours) and lasting for 1-2 days in tissue. Although the most abundant leukocyte in the blood the vast majority of neutrophils are found in the bone marrow (5x more) mostly as functionally immature precursor cells, although this varies between species with mice having a large pool of functional neutrophils in their bone marrow. Neutrophils play a key role during bacterial infections and have both phagocytic and killing actions.
Neutrophils are called heterophils in birds, reptiles and some mammals.
Development
The neutrophil is a granulocyte and has a similar development to the other granulocytes; this process is called granulopoiesis.
Granules
Three types of granules are present in neutrophils:
- Primary granules (azurophilic) are present in all granulocytes and contain myeloperoxidase which creates anti-bacterial compounds, acid hydrolases and defensins.
- Secondary granules (specific) are the most numerous type and contain complement activators and enzymes e.g. collagenases.
- Finally tertiary granules are either phosphatases or metalloproteinases with the later aiding movement through connective tissue.
Movement
Neutrophils are extremely motile and express a number of adhesion molecules on their surface which allows them to attach to the walls of capillaries.
Selection molecules expressed on the surface of neutrophil bind to receptors on the capillary endothelium causing a loose attachment. This allows the neutrophil to “roll” along the surface of capillaries. Stimulation by chemokines causes further attachment between the neutrophils intergrin molecules and associated receptors on the endothelium. Finally signalling molecules or cytokines such as tumour necrosis factors (TNF) and interleukin 1 (Il-1) cause the expression of inter-cellular adhesion molecule 1 (ICAM-1) and vascular cell adhesion molecule 1 (VCAM-1) on the neutrophil which causes firm attachment.
The neutrophil then exhibits amoeboid movement and can pass through holes in the capillary wall that are smaller than themselves (diapedesis). This is achieved by extending a small part of the cell (a pseudopodium) through the capillary; the neutrophil's cytoplasm and contents then passes through. This process is assisted by the release of histamine and other vasodilators by other inflammatory cells.
Once within the tissue, neutrophils respond to chemotactic substances such as cytokines or bacterial products which attract the neutrophil to the area of damage/ infection. This process is called chemotaxis. Once neutrophils have entered tissue they do not return to the blood stream.
Actions
Neutrophils are the first inflammatory cells to enter damaged tissue from the blood after tissue damage has being caused. They are the predominant cell 4 - 6 hours after the beginning of an inflammatory reaction; at 12 hours there are also substantial numbers of macrophages and at 24 hours there are equal numbers of neutrophils and macrophages.
Phagocytosis
The main role of the neutrophil is to engulf and destroy foreign material through phagocytosis. They uptake this material via endocytosis and this surrounds the material in the neutrophil membrane forming a phagosome. Lysosomes inside the neutrophil then fuse with the phagosome and release their contents degrading the foreign material. Phagocytosing material shortens the lifespan of the neutrophil due to the build up of toxins both from the degraded bacteria etc. and also from its own lysosomes contents. Most neutrophils die after phagocytosing 5-25 bacteria; sufficient numbers of dead neutrophils form pus.
Neutrophils do not always destroy engulfed particles and may instead transport them to local lymph nodes to be dealt with by other host defence mechanisms. This means that acute inflammation in tissue can be accompanied by an acute inflammation in the lymph nodes.
Recognition
To function correctly neutrophils need to correctly identify material that is either foreign (non-self) or which requires removal, such as damaged cells. They are able to recognise some foreign material directly but in other circumstances proteins (opsonins) that bind to bacteria are required to increase the chances of successfully binding the foreign material to the neutrophil.
Killing
This occurs using either oxygen dependant pathways or oxygen independent pathways.
Oxygen dependant killing requires the production of reactive oxygen atoms that damage bacterial membranes. These atoms are generated during a burst of respiration following phagocytosis where increased amounts of oxygen are produced. Hydrochloric acid is also produced during this process.
Oxygen independent killing uses lysosomes, cathepsin (a protease) and other mechanisms. Lysozymes are particularly effective against gram positive bacteria as they hydrolyse the glycopeptide coating of the bacterial organisms.
Exocytosis
This is the process of granule fusion with the plasma membrane, causing the release of the granule contents into the immediate vicinity. Contents can include vasoactive peptides, for example, histamine and bradykinin which, as their name suggests, activate the endothelium. This causes the endothelium to become more "leaky" causing a great increase in extravasation of blood granulocytes and monocytes, and the diffusion of plasma proteins to the site of infection. These peptides, released from other cells as well as neutrophils (e.g. Mast cells, are responsible for the classical signs of inflammation: redness (rubor), heat (calor), swelling (tumor), and pain (dolor), often accompanied by loss of function.
Further amplification of inflammation
Neutrophils have many mechanisms to increase inflammation. These include cytokine release and exocytosis of vasoactive peptides as mentioned above. Neutrophil activation in an inflammatory lesion can also result in the release of prostaglandins, through synthesis by cyclo-oxygenase 2, which are responsible for vasoactive changes and for pain (N.B. These are reduced with cyclo-oxygenase (COX) inhibition for example with the NSAID (non-steriodal anti-inflammatory drugs)'s Aspirin and Ibuprofen).
Interactions
Il-6, Il-8 and C5a are all chemoattractants for neutrophils.
In pathology
- Classically a cell involved in acute inflammation
- Liquefactive necrosis in the formation of pus
- Are pyrogenic (fever producing)
- Neutrophilia/Neutropenia
| Neutrophils Learning Resources | |
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 Selection of relevant PowerPoint tutorials |
Tutorial about histology of blood cells |