Nonspecific immune cell

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A non-specific immune cell is an immune cell (such as a macrophage, neutrophil, or dendritic cell) that responds to many antigens, not just one antigen. Non-specific immune cells function in the first line of defense against infection or injury. The innate immune system is always present at the site of infection and ready to fight the bacteria; it can also be referred to as the "natural" immune system. The cells of the innate immune system do not have specific responses and respond to each foreign invader using the same mechanism. [1]

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The innate immune system

There are two categories to which parts of the immune system are assigned: the non-specific, or innate immune system and the adaptive immune system. The non-specific response is a generalized response to pathogen infections involving the use of several white blood cells and plasma proteins. Non-specific immunity, or innate immunity, is the immune system with which you were born, made up of phagocytes and barriers. Phagocytosis, derived from the Greek words phagein, meaning to eat, kytos or cell, and “osis” meaning process, was first described by Élie Metchnikoff, who won the Nobel Prize 100 years ago. Phagocytosis involves the internalization of solids, such as bacteria, by an organism.

Phagocytosis in Three Steps Phagocytosis in three steps.png
Phagocytosis in Three Steps

Macrophages, neutrophils, and dendritic cells are all cells of the innate immune system that utilize phagocytosis and are equipped with Toll-like receptors (TLR). Toll-like receptors are present on each of these cells and recognize a variety of microbial products resulting in the induction of more specific immune responses. [2] When a phagocytic cell engulfs bacteria, a phagosome is formed around it and the entire complex is ultimately trafficked to the lysosome for degradation. These cells that participate in the non-specific immune system response do not differentiate between types of microorganisms but do have the ability to discern between what is self and what is non-self. The cells of this system are known as non-specific immune cells. [3]

Cells of the innate immune system

Neutrophils are a type of phagocyte, abundant in blood, that phagocytize pathogens in acute inflammation. Neutrophils, along with eosinophils and basophils, make up the category of granulocytes. Macrophages, also known as monocytes, will phagocytize a wide range of molecules. Dendritic cells are tree-like cells that bind antigens and alert the lymphocytes of infection, essentially directing T cells to make an immune response. Complement proteins are proteins that play a role in the non-specific immune responses alongside these non-specific immune cells to make up the first line of immune defense. [4]

The non-specific immune response is an immediate antigen-independent response, however it is not antigen-specific. Non-specific immunity results in no immunologic memory. There are mechanical, chemical, and biological factors affecting the effectiveness and results of the non-specific immune response. These factors include the epithelial surfaces forming a physical barrier, fatty acids that inhibit the growth of bacteria, and the microflora of the gastrointestinal tract serving to prevent the colonization of pathogenic bacteria. The non-specific immune system involves cells to which antigens are not specific in regards to fighting infection. The non-specific immune cells mentioned above (macrophages, neutrophils, and dendritic cells) will be discussed regarding their immediate response to infection. [5]

Macrophages

Macrophage infected with bacteria. Macrophage Infected with Francisella tularensis Bacteria (5950310835).jpg
Macrophage infected with bacteria.

Macrophages display a plasticity that allows them to respond to numerous types of infections, permitting them to change their physiology, while serving as a common “janitorial cell” to the immune system. [6] Macrophages are produced through the differentiation of monocytes, and after ingestion of bacteria, secrete enzymes to destroy the ingested particle. These cells reside in every tissue of the body, and upon infected tissue, are recruited to the tissue. Once recruited, macrophages will differentiate into specific tissue macrophages. The receptors of macrophages consist of a broad specificity that allows them to discern between self and non-self in the non-specific recognition of foreign substances. There are type I and type II receptors present on macrophages, which are trimeric membrane glycoproteins each containing an NH2-terminal intracellular domain, an extracellular domain with a spacer region and an alpha-helical domain. [7] Contrary to the structure of type II, type I receptors have a cysteine-rich COOH-terminal domain. These characteristics of macrophage receptors confer the broad specificity, which allow them to function as a general non-specific immune cell.

Neutrophils

Neutrophil ingesting Methicillin-resistant Staphylococcus aureus (MRSA). Methicillin-resistant Staphylococcus aureus (MRSA) Ingestion by a Neutrophil (6830921049).jpg
Neutrophil ingesting Methicillin-resistant Staphylococcus aureus (MRSA).

Neutrophils are some of the first immune cells to travel to sites of infection that aid in fighting infection by ingesting microorganisms and providing the enzymes to kill them. This process characterizes neutrophils as a type of phagocyte. [8] Neutrophils contain neutrophil extracellular traps (NETs), composed of granule and nuclear constituents, which play a role in breaking up and killing bacteria that has invaded the immune system. NETs, composed of activated neutrophils, are fragile structures consisting of smooth stretches and globular domains, as shown via high-resolution scanning electron microscopy. [9]

After stimulation of the neutrophil response, neutrophils lose their shape, allowing euchromatin and heterochromatin to homogenize, later resulting in the mixing of NET components. The formation of NETs happens once the nuclear envelope and granule membrane of the neutrophils disintegrates. The NETs are released as the cell membrane breaks, resulting in a unique process of cell death. These NET structures of neutrophils bind Gram-positive and Gram-negative bacteria, as well as fungi, which confers broad specificity of neutrophils, explaining their role in the first line of defense once microbes have invaded. [10]

Dendritic cells

Dendritic cell. Follicular Dendritic Cell.jpg
Dendritic cell.

The classification of dendritic cells as another type of white blood cell occurred over thirty-five years ago by Ralph Steinmann and Zanvil A. Cohn and has provided an essential link in the innate immune system. [11] Dendritic cells line airways and intestines, participate in a rich network making up part of the epidermal layer of the skin, and play a unique role in initiating a primary immune response. Dendritic cells are named after their structure that resembles that of a dendrite of an axon, and they have two vital functions: display antigens, which are recognized by T cells and alert lymphocytes of the presence of an injury or infection. When the body is introduced to infection or injury, dendritic cells migrate to immune or lymphoid tissues. These two types of tissues are rich in T cells, the cells whose actions are induced by dendritic cells. Dendritic cells will capture antigens and engulf them through the process of phagocytosis. Dendritic cells contain Toll-like receptors (TLR) that will recognize a broad variety of microorganisms in the case of invasion. [12] The activation of these receptors stimulates specific antigen responses and development of antigen-specific adaptive immunity. A unique feature of dendritic cells is that they are able to open up the tight junctions between epithelial cells and sample invaders themselves, all while maintaining the integrity of the epithelial barrier with expression of their own tight-junction proteins. A real life example of dendritic cell functions is displayed in the rejection of organ transplants.

Related Research Articles

<span class="mw-page-title-main">Immune system</span> Biological system protecting an organism against disease

The immune system is a network of biological processes that protects an organism from diseases. It detects and responds to a wide variety of pathogens, from viruses to parasitic worms, as well as cancer cells and objects such as wood splinters, distinguishing them from the organism's own healthy tissue. Many species have two major subsystems of the immune system. The innate immune system provides a preconfigured response to broad groups of situations and stimuli. The adaptive immune system provides a tailored response to each stimulus by learning to recognize molecules it has previously encountered. Both use molecules and cells to perform their functions.

An immune response is a physiological reaction which occurs within an organism in the context of inflammation for the purpose of defending against exogenous factors. These include a wide variety of different toxins, viruses, intra- and extracellular bacteria, parasites, and fungi which could cause serious problems to the health of the host organism if not cleared from the body.

<span class="mw-page-title-main">Macrophage</span> Type of white blood cell

Macrophages are a type of white blood cell of the innate immune system that engulf and digest pathogens, such as cancer cells, microbes, cellular debris, and foreign substances, which do not have proteins that are specific to healthy body cells on their surface. This process is called phagocytosis, which acts to defend the host against infection and injury.

<span class="mw-page-title-main">Phagocytosis</span> Process by which a cell uses its plasma membrane to engulf a large particle

Phagocytosis is the process by which a cell uses its plasma membrane to engulf a large particle, giving rise to an internal compartment called the phagosome. It is one type of endocytosis. A cell that performs phagocytosis is called a phagocyte.

<span class="mw-page-title-main">Neutrophil</span> Most abundant type of granulocytes and the most abundant white blood cell

Neutrophils are the most abundant type of granulocytes and make up 40% to 70% of all white blood cells in humans. They form an essential part of the innate immune system, with their functions varying in different animals.

<span class="mw-page-title-main">Phagocyte</span> Cells that ingest harmful matter within the body

Phagocytes are cells that protect the body by ingesting harmful foreign particles, bacteria, and dead or dying cells. Their name comes from the Greek phagein, "to eat" or "devour", and "-cyte", the suffix in biology denoting "cell", from the Greek kutos, "hollow vessel". They are essential for fighting infections and for subsequent immunity. Phagocytes are important throughout the animal kingdom and are highly developed within vertebrates. One litre of human blood contains about six billion phagocytes. They were discovered in 1882 by Ilya Ilyich Mechnikov while he was studying starfish larvae. Mechnikov was awarded the 1908 Nobel Prize in Physiology or Medicine for his discovery. Phagocytes occur in many species; some amoebae behave like macrophage phagocytes, which suggests that phagocytes appeared early in the evolution of life.

<span class="mw-page-title-main">Granulocyte</span> Category of white blood cells

Granulocytes are cells in the innate immune system characterized by the presence of specific granules in their cytoplasm. Such granules distinguish them from the various agranulocytes. All myeloblastic granulocytes are polymorphonuclear. They have varying shapes (morphology) of the nucleus ; and are referred to as polymorphonuclear leukocytes. In common terms, polymorphonuclear granulocyte refers specifically to "neutrophil granulocytes", the most abundant of the granulocytes; the other types have varying morphology. Granulocytes are produced via granulopoiesis in the bone marrow.

<span class="mw-page-title-main">Cell-mediated immunity</span> Immune response that does not involve antibodies

Cell-mediated immunity or cellular immunity is an immune response that does not involve antibodies. Rather, cell-mediated immunity is the activation of phagocytes, antigen-specific cytotoxic T-lymphocytes, and the release of various cytokines in response to an antigen.

Opsonins are extracellular proteins that, when bound to substances or cells, induce phagocytes to phagocytose the substances or cells with the opsonins bound. Thus, opsonins act as tags to label things in the body that should be phagocytosed by phagocytes. Different types of things ("targets") can be tagged by opsonins for phagocytosis, including: pathogens, cancer cells, aged cells, dead or dying cells, excess synapses, or protein aggregates. Opsonins help clear pathogens, as well as dead, dying and diseased cells.

<span class="mw-page-title-main">Adaptive immune system</span> Subsystem of the immune system

The adaptive immune system, also known as the acquired immune system, or specific immune system is a subsystem of the immune system that is composed of specialized, systemic cells and processes that eliminate pathogens or prevent their growth. The acquired immune system is one of the two main immunity strategies found in vertebrates.

<span class="mw-page-title-main">Antigen-presenting cell</span> Cell that displays antigen bound by MHC proteins on its surface

An antigen-presenting cell (APC) or accessory cell is a cell that displays antigen bound by major histocompatibility complex (MHC) proteins on its surface; this process is known as antigen presentation. T cells may recognize these complexes using their T cell receptors (TCRs). APCs process antigens and present them to T-cells.

<span class="mw-page-title-main">Phagosome</span>

In cell biology, a phagosome is a vesicle formed around a particle engulfed by a phagocyte via phagocytosis. Professional phagocytes include macrophages, neutrophils, and dendritic cells (DCs).

Gut-associated lymphoid tissue (GALT) is a component of the mucosa-associated lymphoid tissue (MALT) which works in the immune system to protect the body from invasion in the gut.

<span class="mw-page-title-main">Innate immune system</span> One of the two main immunity strategies

The innate, or nonspecific, immune system is one of the two main immunity strategies in vertebrates. The innate immune system is an alternate defense strategy and is the dominant immune system response found in plants, fungi, insects, and primitive multicellular organisms.

<span class="mw-page-title-main">Alveolar macrophage</span>

An alveolar macrophage, pulmonary macrophage, is a type of macrophage, a professional phagocyte, found in the airways and at the level of the alveoli in the lungs, but separated from their walls.

<span class="mw-page-title-main">Neutrophil extracellular traps</span> Networks of fibres which bind pathogens

Neutrophil extracellular traps (NETs) are networks of extracellular fibers, primarily composed of DNA from neutrophils, which bind pathogens. Neutrophils are the immune system's first line of defense against infection and have conventionally been thought to kill invading pathogens through two strategies: engulfment of microbes and secretion of anti-microbials. In 2004, a novel third function was identified: formation of NETs. NETs allow neutrophils to kill extracellular pathogens while minimizing damage to the host cells. Upon in vitro activation with the pharmacological agent phorbol myristate acetate (PMA), Interleukin 8 (IL-8) or lipopolysaccharide (LPS), neutrophils release granule proteins and chromatin to form an extracellular fibril matrix known as NET through an active process.

The mannose receptor is a C-type lectin primarily present on the surface of macrophages, immature dendritic cells and liver sinusoidal endothelial cells, but is also expressed on the surface of skin cells such as human dermal fibroblasts and keratinocytes. It is the first member of a family of endocytic receptors that includes Endo180 (CD280), M-type PLA2R, and DEC-205 (CD205).

<span class="mw-page-title-main">Ocular immune system</span>

The ocular immune system protects the eye from infection and regulates healing processes following injuries. The interior of the eye lacks lymph vessels but is highly vascularized, and many immune cells reside in the uvea, including mostly macrophages, dendritic cells, and mast cells. These cells fight off intraocular infections, and intraocular inflammation can manifest as uveitis or retinitis. The cornea of the eye is immunologically a very special tissue. Its constant exposure to the exterior world means that it is vulnerable to a wide range of microorganisms while its moist mucosal surface makes the cornea particularly susceptible to attack. At the same time, its lack of vasculature and relative immune separation from the rest of the body makes immune defense difficult. Lastly, the cornea is a multifunctional tissue. It provides a large part of the eye's refractive power, meaning it has to maintain remarkable transparency, but must also serve as a barrier to keep pathogens from reaching the rest of the eye, similar to function of the dermis and epidermis in keeping underlying tissues protected. Immune reactions within the cornea come from surrounding vascularized tissues as well as innate immune responsive cells that reside within the cornea.

Adenylate cyclase toxin (CyaA) is released from bacterium Bordetella pertussis by the T1SS and released in the host’s respiratory tract in order to suppress its early innate and subsequent adaptive immune defense.

Phagoptosis is a type of cell death caused by the cell being phagocytosed by another cell, and therefore this form of cell death is prevented by blocking phagocytosis.

References

  1. Alberts B. et al. Molecular Biology of the Cell. 4th edition. New York: Garland Science; 2002. Innate Immunity. Available from: https://www.ncbi.nlm.nih.gov/books/NBK26846/
  2. Lien, Egil; Ingalls, Robin (January 2002). "Toll-like Receptors". Society of Critical Care Medicine. 30 (1).
  3. Lodish, Harvey; Berk, Arnold; Kaiser, Chris; Krieger, Monty; Bretscher, Anthony; Ploegh, Hidde; Amon, Angelika; Scott, Matthew. Molecular Cell Biology (Seventh ed.). W.H. Freeman and Company. pp. 1062–1065.
  4. Muller, Michael. "The Immune System" . Retrieved 15 November 2015.
  5. Mayer, Gene. "Innate (Non-specific) Immunity". Microbiology and Immunology Online.
  6. Mosser DM, Edwards JP (2008). "Exploring the full spectrum of macrophage activation". Nature Reviews Immunology. 8 (12): 958–969. doi:10.1038/nri2448. PMC   2724991 . PMID   19029990.
  7. Elomaa, Outi; Sankala, Marko; Pikkarainen, Timo; Bergmann, Ulrich; Tuuttila, Ari; Sariola, Hannu; Trggvason, Karl; Raatikainen- Ahokas, Anne (20 February 1998). "Structure of the Human Macrophage MARCO Receptor and Characterization of its Bacteria-Binding Region". Journal of Biological Chemistry. 273 (8): 4530–4538. doi: 10.1074/jbc.273.8.4530 . PMID   9468508.
  8. "Neutrophils". PubMed Health. National Cancer Institute.
  9. Brinkman, Volker; Reichard, Ulrike; Goosmann, Christian; Fauler, Beatrix; Uhlemann, Yvonne; Weiss, David; Weinrauch, Yvette; Zychlinsky, Arturo (24 December 2003). "Neutrophil Extracellular Traps Kill Bacteria". Science. 303 (5663): 1532–1535. Bibcode:2004Sci...303.1532B. doi:10.1126/science.1092385. PMID   15001782. S2CID   21628300.
  10. Fuchs Tobias A.; Abed Ulrike; Goosmann Christian; Hurwitz Robert; Schulze Ilka; Wahn Volker; Weinrauch Yvette; Brinkmann Volker; Zychlinsky Arturo (2007). "Novel cell death program leads to neutrophil extracellular traps". J Cell Biol. 176 (2): 231–241. doi:10.1083/jcb.200606027. PMC   2063942 . PMID   17210947.
  11. "Laboratory of Cellular Biology and Physiology". The Rockefeller University. The Rockefeller University. Retrieved 16 November 2015.
  12. Takeda, Kiyoshi; Kaisho, Tsuneyasu; Akira, Shizuo (April 2003). "Toll-Like Receptors". Annual Review of Immunology. 21: 335–376. doi:10.1146/annurev.immunol.21.120601.141126. PMID   12524386.

PD-icon.svg This article incorporates public domain material from Dictionary of Cancer Terms. U.S. National Cancer Institute.