Biology:Secretion

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Secretory mechanism.jpg
Short description: Controlled release of substances by cells or tissues

Secretion is the movement of material from one point to another, such as a secreted chemical substance from a cell or gland. In contrast, excretion is the removal of certain substances or waste products from a cell or organism. The classical mechanism of cell secretion is via secretory portals at the plasma membrane called porosomes.[1] Porosomes are permanent cup-shaped lipoprotein structures embedded in the cell membrane, where secretory vesicles transiently dock and fuse to release intra-vesicular contents from the cell.

Secretion in bacterial species means the transport or translocation of effector molecules. For example: proteins, enzymes or toxins (such as cholera toxin in pathogenic bacteria e.g. Vibrio cholerae) from across the interior (cytoplasm or cytosol) of a bacterial cell to its exterior. Secretion is a very important mechanism in bacterial functioning and operation in their natural surrounding environment for adaptation and survival.

In eukaryotic cells

Porosome

Mechanism

Eukaryotic cells, including human cells, have a highly evolved process of secretion. Proteins targeted for the outside are synthesized by ribosomes docked to the rough endoplasmic reticulum (ER). As they are synthesized, these proteins translocate into the ER lumen, where they are glycosylated and where molecular chaperones aid protein folding. Misfolded proteins are usually identified here and retrotranslocated by ER-associated degradation to the cytosol, where they are degraded by a proteasome. The vesicles containing the properly folded proteins then enter the Golgi apparatus.

In the Golgi apparatus, the glycosylation of the proteins is modified and further post-translational modifications, including cleavage and functionalization, may occur. The proteins are then moved into secretory vesicles which travel along the cytoskeleton to the edge of the cell. More modification can occur in the secretory vesicles (for example insulin is cleaved from proinsulin in the secretory vesicles).

Eventually, there is vesicle fusion with the cell membrane at porosomes, by a process called exocytosis, dumping its contents out of the cell's environment.[2]

Strict biochemical control is maintained over this sequence by usage of a pH gradient: the pH of the cytosol is 7.4, the ER's pH is 7.0, and the cis-golgi has a pH of 6.5. Secretory vesicles have pHs ranging between 5.0 and 6.0; some secretory vesicles evolve into lysosomes, which have a pH of 4.8.

Nonclassical secretion

There are many proteins like FGF1 (aFGF), FGF2 (bFGF), interleukin-1 (IL1) etc. which do not have a signal sequence. They do not use the classical ER-Golgi pathway. These are secreted through various nonclassical pathways.

At least four nonclassical (unconventional) protein secretion pathways have been described.[3] They include:

  • direct protein translocation across the plasma membrane likely through membrane transport proteins
  • blebbing
  • lysosomal secretion
  • release via exosomes derived from multivesicular bodies

In addition, proteins can be released from cells by mechanical or physiological wounding[4] and through non-lethal, transient oncotic pores in the plasma membrane induced by washing cells with serum-free media or buffers.[5]

In human tissues

Many human cell types have the ability to be secretory cells. They have a well-developed endoplasmic reticulum, and Golgi apparatus to fulfill this function. Tissues that produce secretions include the gastrointestinal tract which secretes digestive enzymes and gastric acid, the lungs which secrete surfactants, and sebaceous glands which secrete sebum to lubricate the skin and hair. Meibomian glands in the eyelid secrete meibum to lubricate and protect the eye.

In gram-negative bacteria

Main page: Biology:Bacterial secretion system

Secretion is not unique to eukaryotes – it is also present in bacteria and archaea as well. ATP binding cassette (ABC) type transporters are common to the three domains of life. Some secreted proteins are translocated across the cytoplasmic membrane by the SecYEG translocon, one of two translocation systems, which requires the presence of an N-terminal signal peptide on the secreted protein. Others are translocated across the cytoplasmic membrane by the twin-arginine translocation pathway (Tat). Gram-negative bacteria have two membranes, thus making secretion topologically more complex. There are at least six specialized secretion systems in gram-negative bacteria. Many secreted proteins are particularly important in bacterial pathogenesis.[6]

Type I secretion system (T1SS or TOSS)

T1SS.svg

Type I secretion is a chaperone dependent secretion system employing the Hly and Tol gene clusters. The process begins as a leader sequence on the protein to be secreted is recognized by HlyA and binds HlyB on the membrane. This signal sequence is extremely specific for the ABC transporter. The HlyAB complex stimulates HlyD which begins to uncoil and reaches the outer membrane where TolC recognizes a terminal molecule or signal on HlyD. HlyD recruits TolC to the inner membrane and HlyA is excreted outside of the outer membrane via a long-tunnel protein channel.

Type I secretion system transports various molecules, from ions, drugs, to proteins of various sizes (20 – 900 kDa). The molecules secreted vary in size from the small Escherichia coli peptide colicin V, (10 kDa) to the Pseudomonas fluorescens cell adhesion protein LapA of 520 kDa.[7] The best characterized are the RTX toxins and the lipases. Type I secretion is also involved in export of non-proteinaceous substrates like cyclic β-glucans and polysaccharides.

T2SS.svg

Type II secretion system (T2SS)

Main page: Biology:Type II secretion system

Proteins secreted through the type II system, or main terminal branch of the general secretory pathway, depend on the Sec or Tat system for initial transport into the periplasm. Once there, they pass through the outer membrane via a multimeric (12–14 subunits) complex of pore forming secretin proteins. In addition to the secretin protein, 10–15 other inner and outer membrane proteins compose the full secretion apparatus, many with as yet unknown function. Gram-negative type IV pili use a modified version of the type II system for their biogenesis, and in some cases certain proteins are shared between a pilus complex and type II system within a single bacterial species.

Type III secretion system (T3SS or TTSS)

Main page: Biology:Type III secretion system
T3SS.svg

It is homologous to the basal body in bacterial flagella. It is like a molecular syringe through which a bacterium (e.g. certain types of Salmonella, Shigella, Yersinia, Vibrio) can inject proteins into eukaryotic cells. The low Ca2+ concentration in the cytosol opens the gate that regulates T3SS. One such mechanism to detect low calcium concentration has been illustrated by the lcrV (Low Calcium Response) antigen utilized by Yersinia pestis, which is used to detect low calcium concentrations and elicits T3SS attachment. The Hrp system in plant pathogens inject harpins and pathogen effector proteins through similar mechanisms into plants. This secretion system was first discovered in Yersinia pestis and showed that toxins could be injected directly from the bacterial cytoplasm into the cytoplasm of its host's cells rather than simply be secreted into the extracellular medium.[8]

Type IV secretion system (T4SS or TFSS)

T4SS
T4SS.svg
Type IV secretion system
Identifiers
SymbolT4SS
PfamPF07996
InterProIPR012991
SCOP21gl7 / SCOPe / SUPFAM
TCDB3.A.7
OPM superfamily215
OPM protein3jqo
Main page: Biology:Type IV secretion system

It is homologous to conjugation machinery of bacteria, the conjugative pili. It is capable of transporting both DNA and proteins. It was discovered in Agrobacterium tumefaciens, which uses this system to introduce the T-DNA portion of the Ti plasmid into the plant host, which in turn causes the affected area to develop into a crown gall (tumor). Helicobacter pylori uses a type IV secretion system to deliver CagA into gastric epithelial cells, which is associated with gastric carcinogenesis.[9] Bordetella pertussis, the causative agent of whooping cough, secretes the pertussis toxin partly through the type IV system. Legionella pneumophila, the causing agent of legionellosis (Legionnaires' disease) utilizes a type IVB secretion system, known as the icm/dot (intracellular multiplication / defect in organelle trafficking genes) system, to translocate numerous effector proteins into its eukaryotic host.[10] The prototypic Type IVA secretion system is the VirB complex of Agrobacterium tumefaciens.[11]

Protein members of this family are components of the type IV secretion system. They mediate intracellular transfer of macromolecules via a mechanism ancestrally related to that of bacterial conjugation machineries.[12][13]

Function

The Type IV secretion system (T4SS) is the general mechanism by which bacterial cells secrete or take up macromolecules. Their precise mechanism remains unknown. T4SS is encoded on Gram-negative conjugative elements in bacteria. T4SS are cell envelope-spanning complexes, or, in other words, 11–13 core proteins that form a channel through which DNA and proteins can travel from the cytoplasm of the donor cell to the cytoplasm of the recipient cell. T4SS also secrete virulence factor proteins directly into host cells as well as taking up DNA from the medium during natural transformation.[14]

Structure

As shown in the above figure, TraC, in particular consists of a three helix bundle and a loose globular appendage.[13]

Interactions

T4SS has two effector proteins: firstly, ATS-1, which stands for Anaplasma translocated substrate 1, and secondly AnkA, which stands for ankyrin repeat domain-containing protein A. Additionally, T4SS coupling proteins are VirD4, which bind to VirE2.[15]

Type V secretion system (T5SS)

T5SS.svg

Also called the autotransporter system,[16] type V secretion involves use of the Sec system for crossing the inner membrane. Proteins which use this pathway have the capability to form a beta-barrel with their C-terminus which inserts into the outer membrane, allowing the rest of the peptide (the passenger domain) to reach the outside of the cell. Often, autotransporters are cleaved, leaving the beta-barrel domain in the outer membrane and freeing the passenger domain. Some researchers believe remnants of the autotransporters gave rise to the porins which form similar beta-barrel structures.[citation needed] A common example of an autotransporter that uses this secretion system is the Trimeric Autotransporter Adhesins.[17]

Type VI secretion system (T6SS)

Main page: Biology:Type VI secretion system

Type VI secretion systems were originally identified in 2006 by the group of John Mekalanos at the Harvard Medical School (Boston, USA) in two bacterial pathogens, Vibrio cholerae and Pseudomonas aeruginosa.[18][19] These were identified when mutations in the Hcp and VrgG genes in Vibrio cholerae led to decreased virulence and pathogenicity. Since then, Type VI secretion systems have been found in a quarter of all proteobacterial genomes, including animal, plant, human pathogens, as well as soil, environmental or marine bacteria.[20][21] While most of the early studies of Type VI secretion focused on its role in the pathogenesis of higher organisms, more recent studies suggested a broader physiological role in defense against simple eukaryotic predators and its role in inter-bacteria interactions.[22][23] The Type VI secretion system gene clusters contain from 15 to more than 20 genes, two of which, Hcp and VgrG, have been shown to be nearly universally secreted substrates of the system. Structural analysis of these and other proteins in this system bear a striking resemblance to the tail spike of the T4 phage, and the activity of the system is thought to functionally resemble phage infection.[24]

Release of outer membrane vesicles

In addition to the use of the multiprotein complexes listed above, Gram-negative bacteria possess another method for release of material: the formation of bacterial outer membrane vesicles.[25] Portions of the outer membrane pinch off, forming nano-scale spherical structures made of a lipopolysaccharide-rich lipid bilayer enclosing periplasmic materials, and are deployed for membrane vesicle trafficking to manipulate environment or invade at host–pathogen interface. Vesicles from a number of bacterial species have been found to contain virulence factors, some have immunomodulatory effects, and some can directly adhere to and intoxicate host cells. release of vesicles has been demonstrated as a general response to stress conditions, the process of loading cargo proteins seems to be selective.[26]

In gram-positive bacteria

Main page: Biology:Bacterial secretion system

In some Staphylococcus and Streptococcus species, the accessory secretory system handles the export of highly repetitive adhesion glycoproteins.

See also

References

[27]

  1. ↑ "Neuronal porosome proteome: Molecular dynamics and architecture". Journal of Proteomics 75 (13): 3952–62. July 2012. doi:10.1016/j.jprot.2012.05.017. PMID 22659300. 
  2. ↑ "Discovery of the 'porosome'; the universal secretory machinery in cells". Journal of Cellular and Molecular Medicine 10 (1): 126–31. 2006. doi:10.1111/j.1582-4934.2006.tb00294.x. PMID 16563225. 
  3. ↑ "Unconventional mechanisms of protein transport to the cell surface of eukaryotic cells". Annual Review of Cell and Developmental Biology 24: 287–308. 2008. doi:10.1146/annurev.cellbio.24.110707.175320. PMID 18590485. 
  4. ↑ "Plasma membrane disruption: repair, prevention, adaptation". Annual Review of Cell and Developmental Biology 19: 697–731. 2003. doi:10.1146/annurev.cellbio.19.111301.140101. PMID 14570587. 
  5. ↑ "Protein release through nonlethal oncotic pores as an alternative nonclassical secretory pathway". BMC Cell Biology 12: 46. October 2011. doi:10.1186/1471-2121-12-46. PMID 22008609. 
  6. ↑ Wooldridge, K, ed (2009). Bacterial Secreted Proteins: Secretory Mechanisms and Role in Pathogenesis. Caister Academic Press. ISBN 978-1-904455-42-4. [page needed]
  7. ↑ "Structural features of the Pseudomonas fluorescens biofilm adhesin LapA required for LapG-dependent cleavage, biofilm formation, and cell surface localization". Journal of Bacteriology 196 (15): 2775–88. August 2014. doi:10.1128/JB.01629-14. PMID 24837291. 
  8. ↑ Salyers, A. A. & Whitt, D. D. (2002). Bacterial Pathogenesis: A Molecular Approach, 2nd ed., Washington, D.C.: ASM Press. ISBN:1-55581-171-X[page needed]
  9. ↑ "Helicobacter pylori CagA: a new paradigm for bacterial carcinogenesis". Cancer Science 96 (12): 835–43. December 2005. doi:10.1111/j.1349-7006.2005.00130.x. PMID 16367902. 
  10. ↑ "The versatile bacterial type IV secretion systems". Nature Reviews. Microbiology 1 (2): 137–49. November 2003. doi:10.1038/nrmicro753. PMID 15035043. 
  11. ↑ "Biogenesis, architecture, and function of bacterial type IV secretion systems". Annual Review of Microbiology 59: 451–85. 2005. doi:10.1146/annurev.micro.58.030603.123630. PMID 16153176. 
  12. ↑ "Type IV secretion: the Agrobacterium VirB/D4 and related conjugation systems". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 1694 (1–3): 219–34. November 2004. doi:10.1016/j.bbamcr.2004.02.013. PMID 15546668. 
  13. ↑ 13.0 13.1 "Structural and functional characterization of the VirB5 protein from the type IV secretion system encoded by the conjugative plasmid pKM101". Proceedings of the National Academy of Sciences of the United States of America 100 (26): 15947–52. December 2003. doi:10.1073/pnas.2535211100. PMID 14673074. Bibcode: 2003PNAS..10015947Y. 
  14. ↑ "F factor conjugation is a true type IV secretion system". FEMS Microbiology Letters 224 (1): 1–15. July 2003. doi:10.1016/S0378-1097(03)00430-0. PMID 12855161. 
  15. ↑ "Type IV secretion in the obligatory intracellular bacterium Anaplasma phagocytophilum". Cellular Microbiology 12 (9): 1213–21. September 2010. doi:10.1111/j.1462-5822.2010.01500.x. PMID 20670295. 
  16. ↑ "Protein secretion in the absence of ATP: the autotransporter, two-partner secretion and chaperone/usher pathways of gram-negative bacteria (review)". Molecular Membrane Biology 22 (1–2): 63–72. 2005. doi:10.1080/09687860500063290. PMID 16092525. 
  17. ↑ "Protein secretion systems and adhesins: the molecular armory of Gram-negative pathogens". International Journal of Medical Microbiology 297 (6): 401–15. October 2007. doi:10.1016/j.ijmm.2007.03.017. PMID 17482513. 
  18. ↑ "Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system". Proceedings of the National Academy of Sciences of the United States of America 103 (5): 1528–33. January 2006. doi:10.1073/pnas.0510322103. PMID 16432199. Bibcode: 2006PNAS..103.1528P. 
  19. ↑ "A virulence locus of Pseudomonas aeruginosa encodes a protein secretion apparatus". Science 312 (5779): 1526–30. June 2006. doi:10.1126/science.1128393. PMID 16763151. Bibcode: 2006Sci...312.1526M. 
  20. ↑ "Type VI secretion: a beginner's guide". Current Opinion in Microbiology 11 (1): 3–8. February 2008. doi:10.1016/j.mib.2008.01.006. PMID 18289922. http://sure.sunderland.ac.uk/id/eprint/3062/2/pallen_t6ss_2007_revised.pdf. 
  21. ↑ "The type VI secretion toolkit". EMBO Reports 9 (8): 735–41. August 2008. doi:10.1038/embor.2008.131. PMID 18617888. 
  22. ↑ "What is type VI secretion doing in all those bugs?". Trends in Microbiology 18 (12): 531–7. December 2010. doi:10.1016/j.tim.2010.09.001. PMID 20961764. 
  23. ↑ "The Type VI secretion system - a widespread and versatile cell targeting system". Research in Microbiology 164 (6): 640–54. 2013. doi:10.1016/j.resmic.2013.03.017. PMID 23542428. 
  24. ↑ "Structure and regulation of the type VI secretion system". Annual Review of Microbiology 66: 453–72. 2012. doi:10.1146/annurev-micro-121809-151619. PMID 22746332. 
  25. ↑ "Bacterial outer membrane vesicles and the host–pathogen interaction". Genes & Development 19 (22): 2645–55. November 2005. doi:10.1101/gad.1299905. PMID 16291643. 
  26. ↑ "Release of outer membrane vesicles by Gram-negative bacteria is a novel envelope stress response". Molecular Microbiology 63 (2): 545–58. January 2007. doi:10.1111/j.1365-2958.2006.05522.x. PMID 17163978. 
  27. ↑ Z. Esna Ashari, N. Dasgupta, K. Brayton & S. Broschat, “An optimal set of features for predicting type IV secretion system effector proteins for a subset of species based on a multi-level feature selection approach”, PLOS ONE Journal, 2018, 13, e0197041. (doi.org/10.1371/journal.pone.0197041.)

Further reading

External links

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