Cell–cell fusogens

Cell–cell fusogens are glycoproteins that facilitate the fusion of cell to cell membranes. Cell–cell fusion is critical for the merging of gamete genomes and the development of organs in multicellular organisms. Cell-cell fusion occurs when both actin cytoskeleton and fusogenic proteins properly rearrange across the cell membrane. This process is led by actin-propelled membrane protrusions.[1]

Cell–cell fusion
Identifiers
SymbolEFF-AFF
PfamPF14884
InterProIPR029213
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Identifiers
Effects of EFF-1 and AFF-1 on vesicle morphology.

EFF-AFF are the identifiers for type 1 glycoproteins that makeup cell–cell fusogens. They were first identified when EFF-1 mutants were found to "block cell fusion in all epidermal and vulval epithelia" in the roundworm, Caenorhabditis elegans.[2] EFF-AFF is a family of type I membrane glycoproteins that act as cell–cell fusogens, named from ''Anchor cell fusion failure''. Because it was known that EFF-1 mutants successfully fused the anchor cell and (uterine seam) utse syncytium to produce a continuous uterine-vulval tube, where these connections failed, AFF-1 mutants were discovered. AFF-1 was deemed necessary for this process in addition to the fusion of heterologous cells in C. elegans.[3] The transmembrane forms of these proteins, like most viral fusogens, possess an N-terminal signal sequence followed by a long extracellular portion, a predicted transmembrane domain, and a short intracellular tail. " A striking conservation in the position and number of all 16 cysteines in the extracellular portion" of EFF-AFF proteins from different nematode species suggests that these proteins are folded in a similar 3D structure that is essential for their fusogenic activity.[4] C. elegans AFF-1 and EFF-1 proteins are essential for developmental cell-to-cell fusion and can merge insect cells. "Thus FFs comprise an ancient family of cellular fusogens that can promote fusion when expressed on a viral particle."[5]

Process

Cell–cell fusogens are proteins that promote plasma membrane fusion among different cells. To be considered a fusogen, it must be required for fusion, fuse unfamiliar membranes, and be present on the fusing membrane when need be. These cells include but are not limited too: gametes, trophoblasts, epithelial, and other developmental cells. These fusogens mediate cell-cell fusion and can perform neuron repairs, auto-fusion, and sealing of the phagosomes. Although these proteins promote similar functions among cells, they have individual mechanisms. These are called unilateral (one fusing membrane needed to be present) and bilateral (same or different fusogens present at both membranes) mechanisms. Most fusogen mechanisms begin with hemifusion, but the mechanism for cell-cell fusogens consists of four separate steps.[6]

Step
  1. Cells must identify and be near each other.
  2. Hemifusion occurs.
  3. Fusion pore in hemifusion structure opens, thus allowing for cell contents to merge.
  4. Cells completely join from pore expansion.

Applications

Roles in gamete fertilization

Cell–cell fusogens have several different applications. These chemical agents can play a significant part in sexual and asexual reproduction by promoting the fusion of the membrane bilayers.[6] With sexual reproduction, evidence found to prove that in mice, some mandatory sperm-egg fusogens are responsible for fusion; two particular proteins were IZUMO1 and CD9. After comparing the data of experiments done with plants, fungi, and invertebrates, it was seen that several crucial genes could have been responsible for fertilization. However, like yeasts, there were no genes found to be adequate for the fertilization process.[7] As of late, another protein has been classified as a gamete fusogen (HAP2 or GCS1). Like the previous example, this protein is present in plants, protists, and invertebrates. This fusogen resembles the eukaryotic somatic fusogen mentioned earlier, EFF-1. The presence of HAP2 induces hemifusion and the mixing of cell content.[6] Yet when considering asexual reproduction, somatic cells can also undergo cell-cell fusion or self-fusion. Two particular fusogens observed were SO and MAK-2. Evidence supports that these proteins control and regulate efficient protein concentration and localization.[7]

Roles in neuronal repair

In the medical field, experiments are done to test for the uses of cell-cell fusogens in axonal nerve repairs and to determine their usefulness with other nerve cells. The current method for nerve repair is suturing the cut ends of nerves. This has a long recovery process, with a low functionality rate for the repaired nerves. When considering cell-cell fusogens as a potential answer, researchers divided these fusogens into two groups based on fusion mechanisms: cell aggregation and membrane modification. One fusogen PEG was found to fit in both groups. It was this fusogen that made restoring nerve cells in humans possible. Once operations were within a certain time frame (12 hours for human nerve repair and 24 hours for sciatic rat treatments), patient recovery was almost successful. With this research, there is potential for repairing human nerve grafts. Some potential uses of cell-cell fusogens studied are cancer vaccines and the regeneration of damaged cells. Additionally, any peripheral nerve in the body could be repaired, and transferred tissues could work as soon as the senses return. Finally, any surgery done on nerves could be repaired as well, thus resulting in a quicker recovery.[8]

See also

References
  1. Shilagardi K, Li S, Luo F, Marikar F, Duan R, Jin P, et al. (April 2013). "Actin-propelled invasive membrane protrusions promote fusogenic protein engagement during cell-cell fusion". Science. 340 (6130): 359–63. Bibcode:2013Sci...340..359S. doi:10.1126/science.1234781. PMC 3631436. PMID 23470732.
  2. Mohler WA, Shemer G, del Campo JJ, Valansi C, Opoku-Serebuoh E, Scranton V, et al. (March 2002). "The type I membrane protein EFF-1 is essential for developmental cell fusion". Developmental Cell. 2 (3): 355–62. doi:10.1016/S1534-5807(02)00129-6. PMID 11879640.
  3. Sapir A, Choi J, Leikina E, Avinoam O, Valansi C, Chernomordik LV, et al. (May 2007). "AFF-1, a FOS-1-regulated fusogen, mediates fusion of the anchor cell in C. elegans". Developmental Cell. 12 (5): 683–98. doi:10.1016/j.devcel.2007.03.003. PMC 1975806. PMID 17488621.
  4. Sapir A, Avinoam O, Podbilewicz B, Chernomordik LV (January 2008). "Viral and developmental cell fusion mechanisms: conservation and divergence". Developmental Cell. 14 (1): 11–21. doi:10.1016/j.devcel.2007.12.008. PMC 3549671. PMID 18194649.
  5. Avinoam O, Fridman K, Valansi C, Abutbul I, Zeev-Ben-Mordehai T, Maurer UE, et al. (April 2011). "Conserved eukaryotic fusogens can fuse viral envelopes to cells". Science. 332 (6029): 589–92. Bibcode:2011Sci...332..589A. doi:10.1126/science.1202333. PMC 3084904. PMID 21436398.
  6. Brukman NG, Uygur B, Podbilewicz B, Chernomordik LV (May 2019). "How cells fuse". The Journal of Cell Biology. 218 (5): 1436–1451. doi:10.1083/jcb.201901017. PMC 6504885. PMID 30936162.
  7. Aguilar PS, Baylies MK, Fleissner A, Helming L, Inoue N, Podbilewicz B, et al. (July 2013). "Genetic basis of cell-cell fusion mechanisms". Trends in Genetics. 29 (7): 427–37. doi:10.1016/j.tig.2013.01.011. PMC 4022042. PMID 23453622.
  8. Abdou SA, Henderson PW (January 2019). "Fusogens: Chemical Agents That Can Rapidly Restore Function After Nerve Injury". The Journal of Surgical Research. 233: 36–40. doi:10.1016/j.jss.2018.07.013. PMID 30502271. S2CID 54563954.
This article incorporates text from the public domain Pfam and InterPro: IPR029213
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