View source for Neutrophils

==Introduction==
[[Image:LH Neutrophil Histology Smaller.jpg|200px|thumb|right|<div style="text-align: center;"><p>'''Higher power'''</p><sup>©RVC 2008</sup></div>]] 
[[Image:LH Neutrophil Histology.jpg|200px|thumb|right|<div style="text-align: center;"><p>'''Lower power'''</p><sup>©RVC 2008</sup></div>]]
[[Image:LH_Avian_Heterophils_Histology.jpg|thumb|200px|right|<div style="text-align: center;"><p>'''Avian Heterophil'''</p><sup>©RVC 2008</sup></div>]]
Neutrophils represent up to 70% of all [[Leukocytes|leukocytes]] in the blood stream (in humans there are approximately 4.4 million neutrophils / millilitre of blood) 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 - Anatomy & Physiology|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.
<p>Neutrophils are called '''[[Heterophils|heterophils]]''' in birds, reptiles and some mammals.</p>

==Development==
The neutrophil is a [[Blood Cells - Overview|granulocyte]] and has a similar development to the other granulocytes; this process is called [[Leukopoiesis#Granulopoiesis|granulopoiesis]].

==Granules==
Three types of granules are present in neutrophils:
*Primary granules (azurophilic) are present in all [[Blood Cells - Overview|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==
[[File:Extravasation.png|thumb|right|300px|Extravasation (the Movement of Leukocytes from the Bloodstream) - R.J. Francis, RVC 2012]]
<p>Neutrophils are extremely motile and express a number of adhesion molecules on their surface which allows them to attach to the walls of capillaries. </p>
<p>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|cytokines]] such as tumour necrosis factor alpha (TNF-α) 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 enothelium enabling the neutrophils to form a firm attachment through the β2 integrin adhesion molecules (in particular LFA-1). </p>
<p>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.</p>
<p>Once within the tissue, neutrophils respond to chemotactic substances such as [[Cytokines|cytokines]] or bacterial products which attract the neutrophil to the area of damage/ infection. This process is called '''chemotaxis''' (see below for a link to a video of this process). Once neutrophils have entered tissue they do not return to the blood stream but instead undergo cell death (see below) .</p>

==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|macrophages]] and at 24 hours there are equal numbers of neutrophils and macrophages. 

===Phagocytosis===
<p>The main role of the neutrophil is to engulf and destroy foreign material through [[Phagocytosis|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 undergo programmed cell death after phagocytosing 5-25 bacteria (see below) </p>
<p>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.</p>

===Recognition===
<p>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. Some examples of opsonins include [[Complement|complement]] component C3bi and bound [[Immunoglobulins|antibody]].  </p>

===Killing===
<p>This occurs using either oxygen dependant pathways or oxygen independent pathways.</p>
<p>'''Oxygen dependant''' killing requires the production of reactive oxygen species (ROS)(O<sub>2</sub><sup>-</sup>), hydrogen peroxide (OH), reactive nitrogen species (RNS) (nitric oxide (NO)) and chlorine (Cl*) free-radicals that damage bacterial membranes (OH + Cl* = HOCl (otherwise known as bleach!)). These reactive species are generated during a burst of respiration following [[Phagocytosis|phagocytosis]] where increased amounts of oxygen are produced. Hydrochloric acid (HCl) is also produced during this process.</p>
<p>'''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. </p>

===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 anti-microbial peptides and enzymes, as well as vasoactive peptides, for example, histamine and bradykinin. These vasoactive peptides can, 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 - Introduction|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 [[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).

===Interactions===
<p>IL-6, IL-8 and [[Complement| complement]] component C5a and C3a are all chemoattractants for neutrophils, as well as bacteria specific peptides, for example fMLP (N-formylated Met-Leu-Phe). These are only a few examples of many chemoattractants that interact with neutrophils.</p>

===Cell Death===
Neutrophils have a limited life span as they cannot synthesise protein or produce ATP through the electron transfer chain in mitochondria. They hence undergo a process called '''apoptosis''' (otherwise reffered to as ''Programmed Cell Death'' or ''Cell Suicide''). This enables the neutrophils to be cleared by tissue [[Macrophages|macrophages]], and therefore the physiological resolution of inflammation. However, in pathological conditions, where the neutrophils that have undergone apoptosis cannot be cleared as there are too few macrophages, or the pathogen is causing the death of the neutrophils, they undergo a process called '''necrosis'''. This results in the release of all of the intracellular contents, and therefore the amplification of the inflammatory response. It is these neutrophils that have undergone necrosis that forms what is known as [[Necrosis - Pathology#Pus Formation|'''pus''']].

==In pathology==
*Classically a cell involved in [[Acute Inflammation|acute inflammation]]
*[[Necrosis - Pathology#Liquefactive Necrosis|Liquefactive necrosis]] in the formation of [[Necrosis - Pathology#Pus Formation|pus]]
*Neutrophils are pyrogenic (fever producing)
*[[Neutrophilia|Neutrophilia]]/[[Neutropenia|Neutropenia]]
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{{Template:Learning
|powerpoints = [[Blood and Haemopoiesis resource|Tutorial about histology of blood cells]]
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==Links==
*[http://www.youtube.com/watch?v=I_xh-bkiv_c&feature=fvwrel Video of chemotaxis and phagocytosis]
*[http://www.youtube.com/watch?v=9wxK6oLA5oc Z Stack (3D) of Many Neutrophils Extravasating out of a Blood Vessel]
*[http://www.youtube.com/watch?v=ZUUfdP87Ssg&feature=related Chemotaxis in Response to an Artificial Stimulus (out of a micropipette)]
*[http://www.youtube.com/watch?v=bnSr_UjKXTo&feature=related Necrosis of a Neutrophil]


{{Robert J Francis
|date = May 3, 2012}}

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[[Category:Blood_Cells]] [[Category:Robert J Francis reviewed]]