Cell signaling

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For the journal, see Cellular Signalling.

Cell signalling is part of a complex system of communication that governs basic cellular activities and coordinates cell actions. The ability of cells to perceive and correctly respond to their microenvironment is the basis of development, tissue repair, and immunity as well as normal tissue homeostasis. Errors in cellular information processing are responsible for diseases such as cancer, autoimmunity, and diabetes. By understanding cell signalling, diseases may be treated effectively and, theoretically, artificial tissues may be created.[citation needed]

Traditional work in biology has focused on studying individual parts of cell signaling pathways. Systems biology research helps us to understand the underlying structure of cell signaling networks and how changes in these networks may affect the transmission and flow of information. Such networks are complex systems in their organization and may exhibit a number of emergent properties including bistability and ultrasensitivity. Analysis of cell signaling networks requires a combination of experimental and theoretical approaches including the development and analysis of simulations and modeling.[citation needed] Long-range allostery is often a significant component of cell signaling events.[1]

Unicellular and multicellular organism cell signaling[edit]

Figure 1. Example of signaling between bacteria. Salmonella enteritidis uses acyl-homoserine lactone for Quorum sensing (see: Inter-Bacterial Communication)

Cell signaling has been most extensively studied in the context of human diseases and signaling between cells of a single organism. However, cell signaling may also occur between the cells of two different organisms. In many mammals, early embryo cells exchange signals with cells of the uterus.[2] In the human gastrointestinal tract, bacteria exchange signals with each other and with human epithelial and immune system cells.[3] For the yeast Saccharomyces cerevisiae during mating, some cells send a peptide signal (mating factor pheromones) into their environment. The mating factor peptide may bind to a cell surface receptor on other yeast cells and induce them to prepare for mating.[4]

Classification[edit]

Main article: Endocrine System

Signaling within, between, and among cells is subdivided into the following classifications:

  • Intracrine signals are produced by the target cell that stay within the target cell.
  • Autocrine signals are produced by the target cell, are secreted, and effect the target cell itself via receptors. Sometimes autocrine cells can target cells close by if they are the same type of cell as the emitting cell. An example of this are immune cells.
  • Juxtacrine signals target adjacent (touching) cells. These signals are transmitted along cell membranes via protein or lipid components integral to the membrane and are capable of affecting either the emitting cell or cells immediately adjacent.
  • Paracrine signals target cells in the vicinity of the emitting cell. Neurotransmitters represent an example.
  • Endocrine signals target distant cells. Endocrine cells produce hormones that travel through the blood to reach all parts of the body.
Figure 2. Notch-mediated juxtacrine signal between adjacent cells.

Cells communicate with each other via direct contact (juxtacrine signaling), over short distances (paracrine signaling), or over large distances and/or scales (endocrine signaling).

Some cell–cell communication requires direct cell–cell contact. Some cells can form gap junctions that connect their cytoplasm to the cytoplasm of adjacent cells. In cardiac muscle, gap junctions between adjacent cells allows for action potential propagation from the cardiac pacemaker region of the heart to spread and coordinately cause contraction of the heart.

The notch signaling mechanism is an example of juxtacrine signaling (also known as contact-dependent signaling) in which two adjacent cells must make physical contact in order to communicate. This requirement for direct contact allows for very precise control of cell differentiation during embryonic development. In the worm Caenorhabditis elegans, two cells of the developing gonad each have an equal chance of terminally differentiating or becoming a uterine precursor cell that continues to divide. The choice of which cell continues to divide is controlled by competition of cell surface signals. One cell will happen to produce more of a cell surface protein that activates the Notch receptor on the adjacent cell. This activates a feedback loop or system that reduces Notch expression in the cell that will differentiate and that increases Notch on the surface of the cell that continues as a stem cell.[5]

Many cell signals are carried by molecules that are released by one cell and move to make contact with another cell. Endocrine signals are called hormones. Hormones are produced by endocrine cells and they travel through the blood to reach all parts of the body. Specificity of signaling can be controlled if only some cells can respond to a particular hormone. Paracrine signals such as retinoic acid target only cells in the vicinity of the emitting cell.[6] Neurotransmitters represent another example of a paracrine signal. Some signaling molecules can function as both a hormone and a neurotransmitter. For example, epinephrine and norepinephrine can function as hormones when released from the adrenal gland and are transported to the heart by way of the blood stream. Norepinephrine can also be produced by neurons to function as a neurotransmitter within the brain.[7] Estrogen can be released by the ovary and function as a hormone or act locally via paracrine or autocrine signaling.[8] Active species of oxygen and nitric oxide can also act as cellular messengers. This process is dubbed redox signaling.

Cell signaling in multicellular organisms[edit]

In a multicellular organism, signaling between cells occurs either through release into the extracellular space, divided in paracrine signaling (over short distances) and endocrine signaling (over long distances), or by direct contact, known as juxtacrine signaling.[9] Autocrine signaling is a special case of paracrine signaling where the secreting cell has the ability to respond to the secreted signaling molecule.[10] Synaptic signaling is a special case of paracrine signaling (for chemical synapses) or juxtacrine signaling (for electrical synapses) between neurons and target cells. Signaling molecules interact with a target cell as a ligand to cell surface receptors, and/or by entering into the cell through its membrane or endocytosis for intracrine signaling. This generally results in the activation of second messengers, leading to various physiological effects.

A particular molecule is generally used in diverse modes of signaling, and therefore a classification by mode of signaling is not possible. At least three important classes of signaling molecules are widely recognized, although non-exhaustive and with imprecise boundaries, as such membership is non-exclusive and depends on the context:

Signaling molecules can belong to several chemical classes: lipids, phospholipids, amino acids, monoamines, proteins, glycoproteins, or gases. Signaling molecules binding surface receptors are generally large and hydrophilic (e.g. TRH, Vasopressin, Acetylcholine), while those entering the cell are generally small and hydrophobic (e.g. glucocorticoids, thyroid hormones, cholecalciferol, retinoic acid), but important exceptions to both are numerous, and a same molecule can act both via surface receptor or in an intracrine manner to different effects.[10] In intracrine signaling, once inside the cell, a signaling molecule can bind to intracellular receptors, other elements, or stimulate enzyme activity (e.g. gasses). The intracrine action of peptide hormones remains a subject of debate.[11]

Hydrogen sulfide is produced in small amounts by some cells of the human body and has a number of biological signaling functions. Only two other such gases are currently known to act as signaling molecules in the human body: nitric oxide and carbon monoxide.[12]

Receptors for cell motility and differentiation[edit]

Cells receive information from their neighbors through a class of proteins known as receptors. Notch is a cell surface protein that functions as a receptor. Animals have a small set of genes that code for signaling proteins that interact specifically with Notch receptors and stimulate a response in cells that express Notch on their surface. Molecules that activate (or, in some cases, inhibit) receptors can be classified as hormones, neurotransmitters, cytokines, and growth factors, but all of these are called receptor ligands. The details of ligand-receptor interactions are fundamental to cell signaling.[citation needed]

As shown in Figure 2 (above, left), notch acts as a receptor for ligands that are expressed on adjacent cells. While some receptors are cell surface proteins, others are found inside cells. For example, estrogen is a hydrophobic molecule that can pass through the lipid bilayer of the membranes. As part of the endocrine system, intracellular Estrogen receptors from a variety of cell types can be activated by estrogen produced in the ovaries.

A number of transmembrane receptors[13][14] for small molecules and peptide hormones[15] as well as intracellular receptors for steroid hormones exist, giving cells the ability to respond to a great number of hormonal and pharmacological stimuli. In diseases, often, proteins that interact with receptors are aberrantly activated, resulting in constitutively activated downstream signals.[16]

For several types of intercellular signaling molecules that are unable to permeate the hydrophobic cell membrane due to their hydrophilic nature, the target receptor is expressed on the membrane. When such signaling molecule activates its receptor, the signal is carried into the cell usually by means of a second messenger such as cAMP.[17][18]

Signaling pathways[edit]

Overview of signal transduction pathways.
Figure 3. Diagram showing key components of a signal transduction pathway. See the MAPK/ERK pathway article for details.

In some cases, receptor activation caused by ligand binding to a receptor is directly coupled to the cell's response to the ligand. For example, the neurotransmitter GABA can activate a cell surface receptor that is part of an ion channel. GABA binding to a GABA A receptor on a neuron opens a chloride-selective ion channel that is part of the receptor. GABA A receptor activation allows negatively-charged chloride ions to move into the neuron, which inhibits the ability of the neuron to produce action potentials. However, for many cell surface receptors, ligand-receptor interactions are not directly linked to the cell's response. The activated receptor must first interact with other proteins inside the cell before the ultimate physiological effect of the ligand on the cell's behavior is produced. Often, the behavior of a chain of several interacting cell proteins is altered following receptor activation. The entire set of cell changes induced by receptor activation is called a signal transduction mechanism or pathway.[19]

In the case of Notch-mediated signaling, the signal transduction mechanism can be relatively simple. As shown in Figure 2 (above, left), activation of Notch can cause the Notch protein to be altered by a protease. Part of the Notch protein is released from the cell surface membrane and takes part in gene regulation. Cell signaling research involves studying the spatial and temporal dynamics of both receptors and the components of signaling pathways that are activated by receptors in various cell types.[citation needed]

A more complex signal transduction pathway is shown in Figure 3. This pathway involves changes of protein-protein interactions inside the cell, induced by an external signal. Many growth factors bind to receptors at the cell surface and stimulate cells to progress through the cell cycle and divide. Several of these receptors are kinases that start to phosphorylate themselves and other proteins when binding to a ligand. This phosphorylation can generate a binding site for a different protein and thus induce protein-protein interaction. In Figure 3, the ligand (called epidermal growth factor (EGF)) binds to the receptor (called EGFR). This activates the receptor to phosphorylate itself. The phosphorylated receptor binds to an adaptor protein (GRB2), which couples the signal to further downstream signaling processes. For example, one of the signal transduction pathways that are activated is called the mitogen-activated protein kinase (MAPK) pathway. The signal transduction component labeled as "MAPK" in the pathway was originally called "ERK," so the pathway is called the MAPK/ERK pathway. The MAPK protein is an enzyme, a protein kinase that can attach phosphate to target proteins such as the transcription factor MYC and, thus, alter gene transcription and, ultimately, cell cycle progression. Many cellular proteins are activated downstream of the growth factor receptors (such as EGFR) that initiate this signal transduction pathway.[citation needed]

Some signaling transduction pathways respond differently, depending on the amount of signaling received by the cell. For instance, the hedgehog protein activates different genes, depending on the amount of hedgehog protein present.[citation needed]

Complex multi-component signal transduction pathways provide opportunities for feedback, signal amplification, and interactions inside one cell between multiple signals and signaling pathways.[citation needed]

Intraspecies and interspecies signaling[edit]

Molecular signaling can occur between different organisms, whether unicellular or multicellular, the emitting organism produces the signaling molecule, secrete it into the environment, where it diffuses, and it is sensed or internalized by the receiving organism. In some cases of interspecies signaling, the emitting organism can actually be a host of the receiving organism, or vice-versa.

Intraspecies signaling occurs especially in bacteria, yeast, social insects, but also many vertebrates. The signaling molecules used by multicellular organisms are often called pheromones, they can have such purposes as alerting against danger, indicating food supply, or assisting in reproduction.[20] In unicellular organisms such as bacteria, signaling can be used to 'activate' peers from a dormant state, enhance virulence, defend against bacteriophages, etc.[21] In quorum sensing, which is also found in social insects, the multiplicity of individual signals has the potentiality to create a positive feedback loop, generating coordinated response, in this context the signaling molecules are called autoinducers.[22][23][24] This signaling mechanism may have been involved in evolution from unicellular to multicellular organisms.[22][25] Bacteria also use contact-dependent signaling, notably to limit their growth.[26]

Molecular signaling can also occur between individuals of different species, this has been particularly studied in bacteria.[27][28][29] Different bacterial species can coordinate to colonize a host and participate in common quorum sensing.[30] Therapeutic strategies to disrupt this phenomenon are being investigated.[31][32] Interactions mediated through signaling molecules are also thought to occur between the gut flora and their host, as part of their commensal or symbiotic relationship.[32][33] Gram negative microbes deploy bacterial outer membrane vesicles for intra- and inter-species signaling in natural environments and at the host-pathogen interface.

See also[edit]

References[edit]

  1. ^ Bu Z, Callaway DJ (2011). "Proteins MOVE! Protein dynamics and long-range allostery in cell signaling". Advances in Protein Chemistry and Structural Biology. Advances in Protein Chemistry and Structural Biology 83: 163–221. doi:10.1016/B978-0-12-381262-9.00005-7. ISBN 978-0-12-381262-9. PMID 21570668. 
  2. ^ Mohamed OA, Jonnaert M, Labelle-Dumais C, Kuroda K, Clarke HJ, Dufort D (June 2005). "Uterine Wnt/β-catenin signaling is required for implantation". Proc Natl Acad Sci U.S.A. 102 (24): 8579–84. doi:10.1073/pnas.0500612102. PMC 1150820. PMID 15930138. 
  3. ^ Clarke MB, Sperandio V (June 2005). "Events at the host-microbial interface of the gastrointestinal tract III. Cell-to-cell signaling among microbial flora, host, and pathogens: there is a whole lot of talking going on". Am. J. Physiol. Gastrointest. Liver Physiol. 288 (6): G1105–9. doi:10.1152/ajpgi.00572.2004. PMID 15890712. 
  4. ^ Lin JC, Duell K, Konopka JB (March 2004). "A Microdomain Formed by the Extracellular Ends of the Transmembrane Domains Promotes Activation of the G Protein-Coupled α-Factor Receptor". Mol Cell Biol 24 (5): 2041–51. doi:10.1128/MCB.24.5.2041-2051.2004. PMC 350546. PMID 14966283. 
  5. ^ Greenwald I (June 1998). "LIN-12/Notch signaling: lessons from worms and flies". Genes Dev 12 (12): 1751–62. doi:10.1101/gad.12.12.1751. PMID 9637676. 
  6. ^ Duester G (September 2008). "Retinoic Acid Synthesis and Signaling during Early Organogenesis". Cell 134 (6): 921–31. doi:10.1016/j.cell.2008.09.002. PMC 2632951. PMID 18805086. 
  7. ^ Cartford MC, Samec A, Fister M, Bickford PC (2004). "Cerebellar norepinephrine modulates learning of delay classical eyeblink conditioning: Evidence for post-synaptic signaling via PKA". Learn Mem 11 (6): 732–7. doi:10.1101/lm.83104. PMC 534701. PMID 15537737. 
  8. ^ Jesmin S, Mowa CN, Sakuma I, et al. (October 2004). "Aromatase is abundantly expressed by neonatal rat penis but downregulated in adulthood". J Mol Endocrinol 33 (2): 343–59. doi:10.1677/jme.1.01548. PMID 15525594. 
  9. ^ Gilbert, Scott F. (2000). "Juxtacrine Signaling". In NCBI bookshelf. Developmental biology (6. ed.). Sunderland, Mass.: Sinauer Assoc. ISBN 0878932437. 
  10. ^ a b Bruce Alberts et al (2002). "General Principles of Cell Communication". In NCBI bookshelf. Molecular biology of the cell (4th ed.). New York: Garland Science. ISBN 0815332181. 
  11. ^ Re, R (October 1999). "The nature of intracrine peptide hormone action". Hypertension 34 (4 Pt 1): 534–8. doi:10.1161/01.HYP.34.4.534. PMID 10523322. 
  12. ^ Hausman, Geoffrey M. Cooper, Robert E. (2000). "Signaling Molecules and Their Receptors". In NCBI bookshelf. The cell : a molecular approach (2nd ed.). Washington, D.C.: ASM Press. ISBN 087893300X. 
  13. ^ Domazet I, Holleran BJ, Martin SS, Lavigne P, Leduc R, Escher E, Guillemette G (2009-05-01). "The Second Transmembrane Domain of the Human Type 1 Angiotensin II Receptor Participates in the Formation of the Ligand Binding Pocket and Undergoes Integral Pivoting Movement during the Process of Receptor Activation". J Biol Chem 284 (18): 11922–9. doi:10.1074/jbc.M808113200. PMC 2673261. PMID 19276075. 
  14. ^ Hislop JN, Henry AG, Marchese A, von Zastrow M (2009-07-17). "Ubiquitination Regulates Proteolytic Processing of G Protein-coupled Receptors after Their Sorting to Lysosomes". J Biol Chem 284 (29): 19361–70. doi:10.1074/jbc.M109.001644. PMC 2740561. PMID 19433584. 
  15. ^ Meng H, Zhang X, Hankenson KD, Wang MM (2009-03-20). "Thrombospondin 2 Potentiates Notch3/Jagged1 Signaling". J Biol Chem 284 (12): 7866–74. doi:10.1074/jbc.M803650200. PMC 2658079. PMID 19147503. 
  16. ^ Copland JA, Sheffield-Moore M, Koldzic-Zivanovic N, Gentry S, Lamprou G, Tzortzatou-Stathopoulou F, Zoumpourlis V, Urban RJ, Vlahopoulos SA (June 2009). "Sex steroid receptors in skeletal differentiation and epithelial neoplasia: is tissue-specific intervention possible?". BioEssays 31 (6): 629–41. doi:10.1002/bies.200800138. PMID 19382224. 
  17. ^ Goh SL, Looi Y, Shen H, Fang J, Bodner C, Houle M, Ng AC, Screaton RA, Featherstone M (2009-07-10). "Transcriptional Activation by MEIS1A in Response to Protein Kinase A Signaling Requires the Transducers of Regulated CREB Family of CREB Co-activators". J Biol Chem 284 (28): 18904–12. doi:10.1074/jbc.M109.005090. PMC 2707216. PMID 19473990. 
  18. ^ Wojtal KA, Hoekstra D, Van IJzendoorn SC (February 2008). "cAMP-dependent protein kinase A and the dynamics of epithelial cell surface domains: moving membranes to keep in shape". BioEssays 30 (2): 146–55. doi:10.1002/bies.20705. PMID 18200529. 
  19. ^ Dinasarapu AR,et al (2011). "Signaling gateway molecule pages—a data model perspective". Bioinformatics 27 (12): 1736–1738. doi:10.1093/bioinformatics/btr190. PMC 3106186. PMID 21505029. 
  20. ^ Tirindelli, R; Dibattista, M; Pifferi, S; Menini, A (July 2009). "From pheromones to behavior". Physiological reviews 89 (3): 921–56. doi:10.1152/physrev.00037.2008. PMID 19584317. 
  21. ^ Mukamolova, GV; Kaprelyants, AS; Young, DI; Young, M; Kell, DB (Jul 21, 1998). "A bacterial cytokine". Proceedings of the National Academy of Sciences of the United States of America 95 (15): 8916–21. doi:10.1073/pnas.95.15.8916. PMC 21177. PMID 9671779. 
  22. ^ a b Miller, Melissa B.; Bassler, Bonnie L. (1 October 2001). "Quorum sensing in bacteria". Annual Review of Microbiology 55 (1): 165–199. doi:10.1146/annurev.micro.55.1.165. PMID 11544353. 
  23. ^ Kaper, JB; Sperandio, V (June 2005). "Bacterial cell-to-cell signaling in the gastrointestinal tract". Infection and immunity 73 (6): 3197–209. doi:10.1128/IAI.73.6.3197-3209.2005. PMC 1111840. PMID 15908344. 
  24. ^ Camilli, A.; Bonnie L. Bassler (24 February 2006). "Bacterial Small-Molecule Signaling Pathways". Science 311 (5764): 1113–1116. doi:10.1126/science.1121357. PMC 2776824. PMID 16497924. 
  25. ^ Stoka, AM (June 1999). "Phylogeny and evolution of chemical communication: an endocrine approach". Journal of molecular endocrinology 22 (3): 207–25. doi:10.1677/jme.0.0220207. PMID 10343281. 
  26. ^ Blango, Matthew G; Mulvey, Matthew A (31 March 2009). "Bacterial landlines: contact-dependent signaling in bacterial populations". Current Opinion in Microbiology 12 (2): 177–181. doi:10.1016/j.mib.2009.01.011. PMC 2668724. PMID 19246237. 
  27. ^ Shank, Elizabeth Anne; Kolter, Roberto (31 March 2009). "New developments in microbial interspecies signaling". Current Opinion in Microbiology 12 (2): 205–214. doi:10.1016/j.mib.2009.01.003. PMC 2709175. PMID 19251475. 
  28. ^ Ryan, R. P.; Dow, J. M. (1 July 2008). "Diffusible signals and interspecies communication in bacteria". Microbiology 154 (7): 1845–1858. doi:10.1099/mic.0.2008/017871-0. 
  29. ^ Ryan, Robert P.; Dow, J. Maxwell (28 February 2011). "Communication with a growing family: diffusible signal factor (DSF) signaling in bacteria". Trends in Microbiology 19 (3): 145–152. doi:10.1016/j.tim.2010.12.003. PMID 21227698. 
  30. ^ Déziel, E; Lépine, F; Milot, S; He, J; Mindrinos, MN; Tompkins, RG; Rahme, LG (Feb 3, 2004). "Analysis of Pseudomonas aeruginosa 4-hydroxy-2-alkylquinolines (HAQs) reveals a role for 4-hydroxy-2-heptylquinoline in cell-to-cell communication". Proceedings of the National Academy of Sciences of the United States of America 101 (5): 1339–44. doi:10.1073/pnas.0307694100. PMC 337054. PMID 14739337. 
  31. ^ Federle, Michael J.; Bassler, Bonnie L. (31 October 2003). "Interspecies communication in bacteria". Journal of Clinical Investigation 112 (9): 1291–1299. doi:10.1172/JCI20195. PMC 228483. PMID 14597753. 
  32. ^ a b Sperandio, V.; et al (14 July 2003). "Bacteria-host communication: The language of hormones". Proceedings of the National Academy of Sciences 100 (15): 8951–8956. doi:10.1073/pnas.1537100100. PMC 166419. 
  33. ^ Hooper, LV; Gordon, JI (May 11, 2001). "Commensal host-bacterial relationships in the gut". Science 292 (5519): 1115–1118. doi:10.1126/science.1058709. PMID 11352068. 

External links[edit]