Chemotaxis

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Capillary tube assay for chemotaxis. Motile prokaryotes sense chemicals in their environment and change their motility accordingly. Absent chemicals, movement is completely random. When an attractant or repellent is present, runs become longer and tumbles become less frequent. The result is net movement towards or away from the chemical (i.e., up up or down the chemical gradient). The net movement can be seen in the beaker, where the bacteria accumulate around the origin of the attractant, and away from the origin of the repellent.

Chemotaxis (from chemo- + taxis) is the movement of an organism in response to a chemical stimulus.[1] Somatic cells, bacteria, and other single-cell or multicellular organisms direct their movements according to certain chemicals in their environment. This is important for bacteria to find food (e.g., glucose) by swimming toward the highest concentration of food molecules, or to flee from poisons (e.g., phenol). In multicellular organisms, chemotaxis is critical to early development (e.g., movement of sperm towards the egg during fertilization) and subsequent phases of development (e.g., migration of neurons or lymphocytes) as well as in normal function. In addition, it has been recognized that mechanisms that allow chemotaxis in animals can be subverted during cancer metastasis.

Positive chemotaxis occurs if the movement is toward a higher concentration of the chemical in question; negative chemotaxis if the movement is in the opposite direction. Chemically prompted kinesis (randomly directed or nondirectional) can be called chemokinesis.

History of chemotaxis research[edit]

Although migration of cells was detected from the early days of the development of microscopy by Leeuwenhoek, a Caltech lecture regarding chemotaxis propounds that 'erudite description of chemotaxis was only first made by T. W. Engelmann (1881) and W. F. Pfeffer (1884) in bacteria, and H. S. Jennings (1906) in ciliates'.[2] The Nobel Prize laureate I. Metchnikoff also contributed to the study of the field during 1882 to 1886, with investigations of the process as an initial step of phagocytosis.[3] The significance of chemotaxis in biology and clinical pathology was widely accepted in the 1930s, and the most fundamental definitions underlying the phenomenon were drafted by this time.[by whom?] The most important aspects in quality control of chemotaxis assays were described by H. Harris in the 1950s.[4] In the 1960s and 1970s, the revolution of modern cell biology and biochemistry provided a series of novel techniques that became available to investigate the migratory responder cells and subcellular fractions responsible for chemotactic activity.[5] The availability of this technology led to the discovery of C5a, a major chemotactic factor involved in acute inflammation. The pioneering works of J. Adler represented a significant turning point in understanding the whole process of intracellular signal transduction of bacteria.[6][non-primary source needed]

Chemoattractants and chemorepellents[edit]

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Chemoattractants and chemorepellents are inorganic or organic substances possessing chemotaxis-inducer effect in motile cells. Effects of chemoattractants are elicited via described or hypothetic chemotaxis receptors, the chemoattractant moiety of a ligand is target cell specific and concentration dependent. Most frequently investigated chemoattractants are formyl peptides and chemokines. Responses to chemorepellents result in axial swimming and they are considered a basic motile phenomena in bacteria. The most frequently investigated chemorepellents are inorganic salts, amino acids, and some chemokines.

Bacterial chemotaxis—general characteristics[edit]

Correlation of swimming behaviour and flagellar rotation

Some bacteria, such as E. coli, have several flagella per cell (4–10 typically). These can rotate in two ways:

  1. Counter-clockwise rotation aligns the flagella into a single rotating bundle, causing the bacterium to swim in a straight line; and
  2. Clockwise rotation breaks the flagella bundle apart such that each flagellum points in a different direction, causing the bacterium to tumble in place.[citation needed]

The directions of rotation are given for an observer outside the cell looking down the flagella toward the cell.[citation needed]

Behavior[edit]

The overall movement of a bacterium is the result of alternating tumble and swim phases.[citation needed] If one watches a bacterium swimming in a uniform environment, its movement will look like a random walk with relatively straight swims interrupted by random tumbles that reorient the bacterium.[citation needed] Bacteria such as E. coli are unable to choose the direction in which they swim, and are unable to swim in a straight line for more than a few seconds due to rotational diffusion; in other words, bacteria "forget" the direction in which they are going.[citation needed] By repeatedly evaluating their course, and adjusting if they are moving in the wrong direction, bacteria can direct their motion to find favorable locations with high concentrations of attractants (usually food) and avoid repellents (usually poisons).[citation needed]

In the presence of a chemical gradient bacteria will chemotax, or direct their overall motion based on the gradient.[citation needed] If the bacterium senses that it is moving in the correct direction (toward attractant/away from repellent), it will keep swimming in a straight line for a longer time before tumbling; however, if it is moving in the wrong direction, it will tumble sooner and try a new direction at random.[citation needed] In other words, bacteria like E. coli use temporal sensing to decide whether their situation is improving or not, and in this way, find the location with the highest concentration of attractant (usually the source) quite well.[citation needed] Even under very high concentrations, it can still distinguish very small differences in concentration, and fleeing from a repellent works with the same efficiency.[citation needed]

This biased random walk is a result of simply choosing between two methods of random movement; namely tumbling and straight swimming.[7] In fact, chemotactic responses such as forgetting direction and choosing movements resemble the decision-making abilities of higher life-forms with brains that process sensory data.[according to whom?][citation needed]

The helical nature of the individual flagellar filament is critical for this movement to occur, and the protein that makes up the flagellar filament, flagellin, is quite similar among all flagellated bacteria.[citation needed] Vertebrates seem to have taken advantage of this fact by possessing an immune receptor (TLR5) designed to recognize this conserved protein.[citation needed]

As in many instances in biology, there are bacteria that do not follow this rule. Many bacteria, such as Vibrio, are monoflagellated and have a single flagellum at one pole of the cell. Their method of chemotaxis is different. Others possess a single flagellum that is kept inside the cell wall. These bacteria move by spinning the whole cell, which is shaped like a corkscrew.[8][page needed]

Signal transduction[edit]

Domain structure of chemotaxis receptor for Asp

Chemical gradients are sensed through multiple transmembrane receptors, called methyl-accepting chemotaxis proteins (MCPs), which vary in the molecules that they detect.[citation needed] These receptors may bind attractants or repellents directly or indirectly through interaction with proteins of periplasmatic space.[citation needed] The signals from these receptors are transmitted across the plasma membrane into the cytosol, where Che proteins are activated.[citation needed] The Che proteins alter the tumbling frequency, and alter the receptors.[citation needed]

Flagellum regulation[edit]

The proteins CheW and CheA bind to the receptor. The absence of receptor activation results in autophosphorylation in the histidine kinase, CheA, at a single highly conserved histidine residue.[9][better source needed] CheA, in turn, transfers phosphoryl groups to conserved aspartate residues in the response regulators CheB and CheY; CheA is a histidine kinase and it does not actively transfer the phosphoryl group, rather, the response regulator CheB takes the phosphoryl group from CheA.[citation needed] This mechanism of signal transduction is called a two-component system, and it is a common form of signal transduction in bacteria.[citation needed] CheY induces tumbling by interacting with the flagellar switch protein FliM, inducing a change from counter-clockwise to clockwise rotation of the flagellum. Change in the rotation state of a single flagellum can disrupt the entire flagella bundle and cause a tumble.[citation needed]

Receptor regulation[edit]

Signalling pathways of E.coli

CheB, when activated by CheA, acts as a methylesterase, removing methyl groups from glutamate residues on the cytosolic side of the receptor; it works antagonistically with CheR, a methyltransferase, which adds methyl residues to the same glutamate residues.[citation needed] If the level of an attractant remains high, the level of phosphorylation of CheA (and, therefore, CheY and CheB) will remain low, the cell will swim smoothly, and the level of methylation of the MCPs will increase (because CheB-P is not present to demethylate).[citation needed] The MCPs no longer respond to the attractant when they are fully methylated; therefore, even though the level of attractant might remain high, the level of CheA-P (and CheB-P) increases and the cell begins to tumble.[citation needed] The MCPs can be demethylated by CheB-P, and, when this happens, the receptors can once again respond to attractants.[citation needed] The situation is the opposite with regard to repellents: fully methylated MCPs respond best to repellents, while least-methylated MCPs respond worst to repellents.[citation needed] This regulation allows the bacterium to 'remember' chemical concentrations from the recent past, a few seconds, and compare them to those it is currently experiencing, thus 'know' whether it is traveling up or down a gradient.[citation needed] Although the methylation system accounts for the wide range of sensitivity[10][non-primary source needed] that bacteria have to chemical gradients, other mechanisms are involved in increasing the absolute value of the sensitivity on a given background. Well-established examples are the ultra-sensitive response of the motor to the CheY-P signal, and the clustering of chemoreceptors.[11][12] [

Eukaryotic chemotaxis[edit]

Difference of gradient sensing in prokaryotes and eukaryotes

The mechanism that eukaryotic cells employ is quite different from that in bacteria; however, sensing of chemical gradients is still a crucial step in the process.[13][better source needed] Due to their size, prokaryotes cannot detect effective concentration gradients; therefore, these cells scan and evaluate their environment by a constant swimming (consecutive steps of straight swims and tumbles). In contrast, the size of eukaryotic cells allows for the possibility of detecting gradients, which results in a dynamic and polarized distribution of receptors; induction of these receptors by chemoattractants or chemorepellents results in migration towards or away from the chemotactic substance.[citation needed]

Levels of receptors, intracellular signalling pathways and the effector mechanisms all represent diverse, eukaryotic-type components. In eukaryotic unicellular cells, amoeboid movement and cilium or the eukaryotic flagellum are the main effectors (e.g., Amoeba or Tetrahymena).[14][15] Some eukaryotic cells of higher vertebrate origin, such as immune cells also move to where they need to be. Besides immune competent cells (granulocyte, monocyte, lymphocyte) a large group of cells—considered previously to be fixed into tissues—are also motile in special physiological (e.g., mast cell, fibroblast, endothelial cells) or pathological conditions (e.g., metastases).[citation needed] Chemotaxis has high significance in the early phases of embryogenesis as development of germ layers is guided by gradients of signal molecules.[citation needed]

Motility[edit]

Unlike motility in bacterial chemotaxis, the mechanism by which eukaryotic cells physically move is unclear. There appear to be mechanisms by which an external chemotactic gradient is sensed and turned into an intracellular PIP3 gradient, which results in a gradient and the activation of a signaling pathway, culminating in the polymerisation of actin filaments. The growing distal end of actin filaments develops connections with the internal surface of the plasma membrane via different sets of peptides and results in the formation of anteriorpseudopods and posterior uropods. Cilia of eukaryotic cells can also produce chemotaxis; in this case, it is mainly a Ca2+-dependent induction of the microtubular system of the basal body and the beat of the 9+2 microtubules within cilia. The orchestrated beating of hundreds of cilia is synchronized by a submembranous system built between basal bodies. The details of the signaling pathways are still not totally clear.

Chemotaxis related migratory responses[edit]

Chemotaxis related migratory responses

Although chemotaxis is the most frequently studied form of migration there are several other forms of locomotion in the cellular level.

  • Chemokinesis is also induced by molecules of the liquid phase of the surrounding environment; however, the response elicited is a not vectorial, random taxis. Neither amplitude nor frequency of motion has characteristic, directional components, as this behaviour provides more scanning of the environment than migration between two distinct points.
  • In haptotaxis the gradient of the chemoattractant is expressed or bound on a surface, in contrast to the classical model of chemotaxis, in which the gradient develops in a soluble fluid. The most common biologically active haptotactic surface is the extracellular matrix (ECM); the presence of bound ligands is responsible for induction of transendothelial migration and angiogenesis.
  • Necrotaxis embodies a special type of chemotaxis when the chemoattractant molecules are released from necrotic or apoptotic cells. Depending on the chemical character of released substances, necrotaxis can accumulate or repel cells, which underlines the pathophysiological significance of this phenomenon.

Receptors[edit]

In general, eukaryotic cells sense the presence of chemotactic stimuli through the use of 7-transmembrane (or serpentine) heterotrimeric G-protein-coupled receptors, a class representing a significant portion of the genome.[citation needed] Some members of this gene superfamily are used in eyesight (rhodopsins) as well as in olfaction (smelling).[citation needed] The main classes of chemotaxis receptors are triggered by:

However, induction of a wide set of membrane receptors (e.g., amino acids, insulin, vasoactive peptides) also elicit migration of the cell.[citation needed]

Chemotactic selection[edit]

Chemotactic selection

While some chemotaxis receptors are expressed in the surface membrane with long-term characteristics, as they are determined genetically, others have short-term dynamics, as they are assembled ad hoc in the presence of the ligand.[citation needed] The diverse features of the chemotaxis receptors and ligands allows for the possibility of selecting chemotactic responder cells with a simple chemotaxis assay.[citation needed] By chemotactic selection, we can determine whether a still-uncharacterized molecule acts via the long- or the short-term receptor pathway.[citation needed] The term chemotactic selection is also used to designate a technique that separates eukaryotic or prokaryotic cells according to their chemotactic responsiveness to selector ligands.[16][non-primary source needed]

Chemotactic ligands[edit]

Structure of chemokine classes
Three dimensional structure of chemokines

The number of molecules capable of eliciting chemotactic responses is relatively high, and we can distinguish primary and secondary chemotactic molecules.[citation needed] The main groups of the primary ligands are as follows:

  • Formyl peptides are di-, tri-, tetrapeptides of bacterial origin, formylated on the N-terminus of the peptide.[citation needed] They are released from bacteria in vivo or after decomposition of the cell[ a typical member of this group is the N-formylmethionyl-leucyl-phenylalanine (abbreviated fMLF or fMLP).[citation needed] Bacterial fMLF is a key component of inflammation has characteristic chemoattractant effects in neutrophil granulocytes and monocytes.[citation needed] The chemotactic factor ligands and receptors related to formyl peptides are summarized in the related article, Formyl peptide receptors.
  • Complement 3a (C3a) and complement 5a (C5a) are intermediate products of the complement cascade.[citation needed] Their synthesis is joined to the three alternative pathways (classical, lectin-dependent, and alternative) of complement activation by a convertase enzyme.[citation needed] The main target cells of these derivatives are neutrophil granulocytes and monocytes as well.[citation needed]
  • Chemokines belong to a special class of cytokines; not only do their groups (C, CC, CXC, CX3C chemokines) represent structurally related molecules with a special arrangement of disulfide bridges but also their target cell specificity is diverse.[citation needed] CC chemokines act on monocytes (e.g., RANTES), and CXC chemokines are neutrophil granulocyte-specific (e.g., IL-8).[citation needed] Investigations of the three-dimensional structures of chemokines provided evidence that a characteristic composition of beta-sheets and an alpha helix provides expression of sequences required for interaction with the chemokine receptors.[citation needed] Formation of dimers and their increased biological activity was demonstrated by crystallography of several chemokines, e.g. IL-8.[citation needed]
  • Metabolites of polyunsaturated fatty acids

Chemotactic range fitting[edit]

Chemotactic range fitting

Chemotactic responses elicited by the ligand-receptor interactions are, in general, distinguished upon the optimal effective concentration(s) of the ligand. Nevertheless, correlation of the amplitude elicited and ratio of the responder cells compared to the total number are also characteristic features of the chemotactic signaling. Investigations of ligand families (e.g., amino acids or oligo peptides) proved that there is a fitting of ranges (amplitudes; number of responder cells) and chemotactic activities: Chemoattractant moiety is accompanied by wide ranges, whereas chemorepellent character by narrow ranges.

Clinical significance[edit]

A changed migratory potential of cells has relatively high importance in the development of several clinical symptoms and syndromes. Altered chemotactic activity of extracellular (e.g., Escherichia coli) or intracellular (e.g., Listeria monocytogenes) pathogens itself represents a significant clinical target. Modification of endogenous chemotactic ability of these microorganisms by pharmaceutical agents can decrease or inhibit the ratio of infections or spreading of infectious diseases. Apart from infections, there are some other diseases wherein impaired chemotaxis is the primary etiological factor, as in Chédiak–Higashi syndrome, where giant intracellular vesicles inhibit normal migration of cells.

Chemotaxis in diseases[citation needed]
Type of disease Chemotaxis increased Chemotaxis decreased
Infections inflammations AIDS, Brucellosis
Chemotaxis results the disease Chédiak–Higashi syndrome, Kartagener syndrome
Chemotaxis is affected atherosclerosis, arthritis, periodontitis, psoriasis, reperfusion injury, metastatic tumors multiple sclerosis, Hodgkin disease, male infertility
Intoxications asbestos, benzpyrene Hg and Cr salts, ozone

Mathematical models[edit]

Several mathematical models of chemotaxis were developed depending on the type of

  • migration (e.g., basic differences of bacterial swimming, movement of unicellular eukaryotes with cilia/flagellum and amoeboid migration)
  • physico-chemical characteristics of the chemicals (e.g., diffusion) working as ligands
  • biological characteristics of the ligands (attractant, neutral, and repellent molecules)
  • assay systems applied to evaluate chemotaxis (see incubation times, development, and stability of concentration gradients)
  • other environmental effects possessing direct or indirect influence on the migration (lighting, temperature, magnetic fields, etc.)

Although interactions of the factors listed above make the behavior of the solutions of mathematical models of chemotaxis rather complex, it is possible to describe the basic phenomenon of chemotaxis-driven motion in a straightforward way. Indeed, let us denote with the spatially non-uniform concentration of the chemo-attractant and with its gradient. Then the chemotactic cellular flow (also called current) that is generated by the chemotaxis is linked to the above gradient by the law: , where is the spatial density of the cells and is the so-called ’Chemotactic coefficient’. However, note that in many cases is not constant: It is, instead, a decreasing function of the concentration of the chemo-attractant : .

Spatial ecology of soil microorganisms is a function of their chemotactic sensitivities towards substrate and fellow organisms.[22][non-primary source needed] The chemotactic behavior of the bacteria was proven to lead to non-trivial population patterns even in the absence of environmental heterogeneities. The presence of structural pore scale heterogeneities has an extra impact on the emerging bacterial patterns.

Measurement of chemotaxis[edit]

A wide range of techniques is available to evaluate chemotactic activity of cells or the chemoattractant and chemorepellent character of ligands. The basic requirements of the measurement are as follows:

  • concentration gradients can develop relatively quickly and persist for a long time in the system
  • chemotactic and chemokinetic activities are distinguished
  • migration of cells is free toward and away on the axis of the concentration gradient
  • detected responses are the results of active migration of cells

Despite the fact that an ideal chemotaxis assay is still not available, there are several protocols and pieces of equipment that offer good correspondence with the conditions described above. The most commonly used are summarised in the table below:

Type of assay Agar-plate assays Two-chamber assays Others
Examples
  • PP-chamber
  • Boyden chamber
  • Zigmond chamber
  • Dunn chambers
  • Multi-well chambers
  • Capillary techniques
  • T-maze technique
  • Opalescence technique
  • Orientation assays

Artificial chemotactic systems[edit]

Chemical robots that use artificial chemotaxis to navigate autonomously have been designed. Applications include targeted delivery of drugs in the body.[23]

See also[edit]

References[edit]

  1. ^ Wikisource-logo.svg Chisholm, Hugh, ed. (1911). "Chemotaxis". Encyclopædia Britannica. 6 (11th ed.). Cambridge University Press. p. 77. 
  2. ^ Chemotaxis Lecture. Uploaded in 2007. available at: http://www.rpgroup.caltech.edu/courses/aph161/2007/lectures/ChemotaxisLecture.pdf (Last inspected: 15/04/17)
  3. ^ Élie Metchnikoff". Encyclopædia Britannica. Encyclopædia Britannica, Inc.
  4. ^ Keller-Segel Models for Chemotaxis. 2012. available at: http://www.isn.ucsd.edu/courses/Beng221/problems/2012/BENG221_Project%20-%20Roberts%20Chung%20Yu%20Li.pdf (Last inspected by April 2017)
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  8. ^ Berg, Howard C. (2003). E. coli in motion. New York, NY: Springer. ISBN 0387008888. [page needed]
  9. ^ ToxCafe (2 June 2011). "Chemotaxis". Retrieved March 23, 2017 – via YouTube. 
  10. ^ Mello BA & Tu Y (2007). "Effects of Adaptation in Maintaining High Sensitivity Over a Wide Range of Backgrounds for Escherichia coli Chemotaxis". Biophysical Journal. 92 (7): 2329–2337. Bibcode:2007BpJ....92.2329M. doi:10.1529/biophysj.106.097808. PMC 1864821Freely accessible. PMID 17208965. [non-primary source needed]
  11. ^ Cluzel P, Surette M & Leibler, S (2000). "An Ultrasensitive Bacterial Motor Revealed by Monitoring Signaling Proteins in Single Cells". Science. 287 (5458): 1652–1655. Bibcode:2000Sci...287.1652C. doi:10.1126/science.287.5458.1652. PMID 10698740. 
  12. ^ Sourjik V & Tso WW (2004). "Receptor clustering and signal processing in E. coli chemotaxis". Trends in Microbiology. 12 (12): 569–576. doi:10.1016/j.tim.2004.10.003. PMID 15539117. 
  13. ^ Köhidai, Laszio (2016), "Chemotaxis as an Expression of Communication of Tetrahymena", in Witzany, G; Nowacki, M, Biocommunication of Ciliates, pp. 65–82, doi:10.1007/978-3-319-32211-7_5, ISBN 978-3-319-32211-7 
  14. ^ Bagorda A & Parent CA (2008). "Eukaryotic chemotaxis at a glance". Journal of Cell Science. 121 (Pt 16): 2621–4. doi:10.1242/jcs.018077. PMID 18685153. 
  15. ^ Laszlo Kohidai (1999). "Chemotaxis: the proper physiological response to evaluate phylogeny of signal molecules". Acta Biol Hung. 50 (4): 375–94. PMID 10735174. 
  16. ^ Laszlo Kohidai and Gyorgy Csaba (1988). "Chemotaxis and chemotactic selection induced with cytokines (IL-8, RANTES and TNF alpha) in the unicellular Tetrahymena pyriformis". Cytokine. 10 (7): 481–6. doi:10.1006/cyto.1997.0328. PMID 9702410. [non-primary source needed]
  17. ^ a b c d Powell WS, Rokach J (2015). "Biosynthesis, biological effects, and receptors of hydroxyeicosatetraenoic acids (HETEs) and oxoeicosatetraenoic acids (oxo-ETEs) derived from arachidonic acid". Biochimica et Biophysica Acta. 1851 (4): 340–55. doi:10.1016/j.bbalip.2014.10.008. PMID 25449650. Retrieved March 23, 2017. 
  18. ^ Powell WS, Rokach J (2013). "The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor". Prog. Lipid Res. 52 (4; October): 651–65. doi:10.1016/j.plipres.2013.09.001. Retrieved March 23, 2017. 
  19. ^ Matsuoka T, Narumiya S (2007). "Prostaglandin receptor signaling in disease". The Scientific World Journal. 7: 1329–47. doi:10.1100/tsw.2007.182. PMID 17767353. [non-primary source needed]
  20. ^ Yokomizo T (2015). "Two distinct leukotriene B4 receptors, BLT1 and BLT2". Journal of Biochemistry. 157 (2): 65–71. doi:10.1093/jb/mvu078. PMID 25480980. [non-primary source needed]
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  22. ^ Gharasoo, Mehdi; Centler, Florian; Fetzer, Ingo; Thullner, Martin (2014). "How the chemotactic characteristics of bacteria can determine their population patterns". Soil Biology and Biochemistry. 69: 346. doi:10.1016/j.soilbio.2013.11.019. [non-primary source needed]
  23. ^ Lagzi, István (2013). "Chemical Robotics—Chemotactic Drug Carriers". Central European Journal of Medicine. 8 (4): 377–382. doi:10.2478/s11536-012-0130-9. 

Further reading[edit]

External links[edit]