Thymosin beta-4

Thymosin beta-4 is a protein that in humans is encoded by the TMSB4X gene.[3][4][5] Recommended INN (International Nonproprietary Name) for thymosin beta-4 is 'timbetasin', as published by the World Health Organization (WHO).[6]

TMSB4X
Available structures PDB Human UniProt search: PDBe RCSB List of PDB id codes 4PL7, 4PL8
Identifiers
Aliases	TMSB4X, FX, PTMB4, TB4X, TMSB4, thymosin beta 4, X-linked, thymosin beta 4 X-linked
External IDs	OMIM: 300159 GeneCards: TMSB4X
Gene location (Human) Chr. X chromosome (human)[1] Band Xp22.2 Start 12,975,110 bp[1] End 12,977,227 bp[1]
RNA expression pattern More reference expression data
Gene ontology Molecular function • actin binding • GO:0001948 protein binding • RNA binding • actin monomer binding • enzyme binding Cellular component • cytoskeleton • platelet alpha granule lumen • intracellular • cell nucleus • cytoplasm • cytosol • extracellular region Biological process • platelet degranulation • actin filament organization • cytoplasmic sequestering of NF-kappaB • negative regulation of NF-kappaB transcription factor activity • tumor necrosis factor-mediated signaling pathway • sequestering of actin monomers • positive regulation of blood vessel endothelial cell migration • regulation of inflammatory response • regulation of NIK/NF-kappaB signaling • negative regulation of NIK/NF-kappaB signaling • negative regulation of RNA polymerase II regulatory region sequence-specific DNA binding • positive regulation of proton-transporting ATP synthase activity, rotational mechanism • negative regulation of interleukin-8 secretion • positive regulation of endothelial cell chemotaxis • positive regulation of ATP biosynthetic process • osteoblast differentiation • regulation of cell migration Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	7114	n/a
Ensembl	ENSG00000205542	n/a
UniProt	P62328	n/a
RefSeq (mRNA)	NM_021109	n/a
RefSeq (protein)	NP_066932	n/a
Location (UCSC)	Chr X: 12.98 – 12.98 Mb	n/a
PubMed search	[2]	n/a
Wikidata
View/Edit Human

The protein consists (in humans) of 43 amino acids (sequence: SDKPDMAEI EKFDKSKLKK TETQEKNPLP SKETIEQEKQ AGES) and has a molecular weight of 4921 g/mol.[7]

Thymosin-β₄ is a major cellular constituent in many tissues. Its intracellular concentration may reach as high as 0.5 mM.[8] Following Thymosin α1, β₄ was the second of the biologically active peptides from Thymosin Fraction 5 to be completely sequenced and synthesized.[9]

Function

This gene encodes an actin sequestering protein which plays a role in regulation of actin polymerization. The protein is also involved in cell proliferation, migration, and differentiation. This gene escapes X inactivation and has a homolog on chromosome Y (TMSB4Y).[5]

Biological activities of thymosin β₄

Any concepts of the biological role of thymosin β₄ must inevitably be coloured by the demonstration that total ablation of the thymosin β₄ gene in the mouse allows apparently normal embryonic development of mice which are fertile as adults.[10]

Actin binding

Thymosin β₄ was initially perceived as a thymic hormone. However this changed when it was discovered that it forms a 1:1 complex with G (globular) actin, and is present at high concentration in a wide range of mammalian cell types.[11] When appropriate, G-actin monomers polymerize to form F (filamentous) actin, which, together with other proteins that bind to actin, comprise cellular microfilaments. Formation by G-actin of the complex with β-thymosin (= "sequestration") opposes this.

Due to its profusion in the cytosol and its ability to bind G-actin but not F-actin, thymosin β₄ is regarded as the principal actin-sequestering protein in many cell types. Thymosin β₄ functions like a buffer for monomeric actin as represented in the following reaction:[12]

F-actin ↔ G-actin + Thymosin β₄ ↔ G-actin/Thymosin β₄

Release of G-actin monomers from thymosin β₄ occurs as part of the mechanism that drives actin polymerization in the normal function of the cytoskeleton in cell morphology and cell motility.

The sequence LKKTET, which starts at residue 17 of the 43-aminoacid sequence of thymosin beta-4, and is strongly conserved between all β-thymosins, together with a similar sequence in WH2 domains, is frequently referred to as "the actin-binding motif" of these proteins, although modelling based on X-ray crystallography has shown that essentially the entire length of the β-thymosin sequence interacts with actin in the actin-thymosin complex.[13]

"Moonlighting"

In addition to its intracellular role as the major actin-sequestering molecule in cells of many multicellular animals, thymosin β₄ shows a remarkably diverse range of effects when present in the fluid surrounding animal tissue cells. Taken together, these effects suggest that thymosin has a general role in tissue regeneration. This has suggested a variety of possible therapeutic applications, and several have now been extended to animal models and human clinical trials.

It is considered unlikely that thymosin β₄ exerts all these effects via intracellular sequestration of G-actin. This would require its uptake by cells, and moreover, in most cases the cells affected already have substantial intracellular concentrations.

The diverse activities related to tissue repair may depend on interactions with receptors quite distinct from actin and possessing extracellular ligand-binding domains. Such multi-tasking by, or "partner promiscuity" of, proteins has been referred to as protein moonlighting.[14] Proteins such as thymosins which lack stable folded structure in aqueous solution, are known as intrinsically unstructured proteins (IUPs). Because IUPs acquire specific folded structures only on binding to their partner proteins, they offer special possibilities for interaction with multiple partners.[15] A candidate extracellular receptor of high affinity for thymosin β₄ is the β subunit of cell surface-located ATP synthase, which would allow extracellular thymosin to signal via a purinergic receptor.[16]

Some of the multiple activities of thymosin β₄ unrelated to actin may be mediated by a tetrapeptide enzymically-cleaved from its N-terminus, N-acetyl-ser-asp-lys-pro, brand names Seraspenide or Goralatide, best known as an inhibitor of the proliferation of haematopoietic (blood-cell precursor) stem cells of bone marrow.

Tissue regeneration

Work with cell cultures and experiments with animals have shown that administration of thymosin β₄ can promote migration of cells, formation of blood vessels, maturation of stem cells, survival of various cell types and lowering of the production of pro-inflammatory cytokines. These multiple properties have provided the impetus for a worldwide series of on-going clinical trials of potential effectiveness of thymosin β₄ in promoting repair of wounds in skin, cornea and heart.[17]

Such tissue-regenerating properties of thymosin β₄ may ultimately contribute to repair of human heart muscle damaged by heart disease and heart attack. In mice, administration of thymosin β₄ has been shown to stimulate formation of new heart muscle cells from otherwise inactive precursor cells present in the outer lining of adult hearts,[18] to induce migration of these cells into heart muscle[19] and recruit new blood vessels within the muscle.[20]

Anti-inflammatory role for sulfoxide

In 1999 researchers in Glasgow University found that an oxidised derivative of thymosin β₄ (the sulfoxide, in which an oxygen atom is added to the methionine near the N-terminus) exerted several potentially anti-inflammatory effects on neutrophil leucocytes. It promoted their dispersion from a focus, inhibited their response to a small peptide (F-Met-Leu-Phe) which attracts them to sites of bacterial infection and lowered their adhesion to endothelial cells. (Adhesion to endothelial cells of blood vessel walls is pre-requisite for these cells to leave the bloodstream and invade infected tissue). A possible anti-inflammatory role for the β₄ sulfoxide was supported by the group's finding that it counteracted artificially-induced inflammation in mice.

The group had first identified the thymosin sulfoxide as an active factor in culture fluid of cells responding to treatment with a steroid hormone, suggesting that its formation might form part of the mechanism by which steroids exert anti-inflammatory effects. Extracellular thymosin β₄ would be readily oxidised to the sulfoxide in vivo at sites of inflammation, by the respiratory burst.[21]

Terminal deoxynucleotidyl transferase

Thymosin β₄ induces the activity of the enzyme terminal deoxynucleotidyl transferase in populations of thymocytes (thymus-derived lymphocytes). This suggests that the peptide may contribute to the maturation of these cells.[9]

Clinical significance

Tβ4 has been studied in a number of clinical trials.[22]

In phase 2 trials with patients having pressure ulcers, venous pressure ulcers, and epidermolysis bullosa, Tβ4 accelerated the rate of repair. It was also found to be safe and well tolerated.[23]

In human clinical trials, Tβ4 improves the conditions of dry eye and neurotrophic keratopathy with effects lasting long after the end of treatment.[24]

See also: Thymosin_beta-4 § Tissue_regeneration

Doping in Sports

See also: Essendon Football Club supplements saga and Drugs in sport in Australia

Thymosin beta-4 was allegedly used by some players in various Australian football codes and is under investigation by the Australian Sports Anti-Doping Authority for anti-doping violations.[25][26]

On 30 March 2015, the Australian Football League anti-doping tribunal initially cleared players of the Essendon Football Club over the use of thymosin beta-4, however after an appeal by the World Anti-Doping Agency, this was overturned on 12 January 2016.[27]

Interactions

TMSB4X has been shown to interact with ACTA1[28][29] and ACTG1.[30][31]

See also

• Beta thymosins
• Thymosin beta-4, Y-chromosomal
• Thymosins

References

1. GRCh38: Ensembl release 89: ENSG00000205542 - Ensembl, May 2017
2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
3. Gómez-Márquez J, Dosil M, Segade F, Bustelo XR, Pichel JG, Dominguez F, Freire M (Oct 1989). "Thymosin-beta 4 gene. Preliminary characterization and expression in tissues, thymic cells, and lymphocytes". Journal of Immunology. 143 (8): 2740–4. PMID 2677145.
4. Lahn BT, Page DC (Oct 1997). "Functional coherence of the human Y chromosome". Science. 278 (5338): 675–80. Bibcode:1997Sci...278..675L. doi:10.1126/science.278.5338.675. PMID 9381176.
5. "Entrez Gene: TMSB4X thymosin, beta 4, X-linked".
6. "Lists of Recommended and Proposed INNs: List 80". 2018.
7. "protein NP_066932". NCBI.
8. Hannappel E (September 2007). "beta-Thymosins". Annals of the New York Academy of Sciences. 1112 (1): 21–37. Bibcode:2007NYASA1112...21H. doi:10.1196/annals.1415.018. PMID 17468232.
9. Low TL, Hu SK, Goldstein AL (February 1981). "Complete amino acid sequence of bovine thymosin beta 4: a thymic hormone that induces terminal deoxynucleotidyl transferase activity in thymocyte populations". Proceedings of the National Academy of Sciences of the United States of America. 78 (2): 1162–6. Bibcode:1981PNAS...78.1162L. doi:10.1073/pnas.78.2.1162. PMC 319967. PMID 6940133.
10. Banerjee I, Zhang J, Moore-Morris T, Lange S, Shen T, Dalton ND, Gu Y, Peterson KL, Evans SM, Chen J (Feb 2012). "Thymosin beta 4 is dispensable for murine cardiac development and function". Circ Res. 110 (3): 456–64. doi:10.1161/CIRCRESAHA.111.258616. PMC 3739283. PMID 22158707.
11. Safer D, Elzinga M, Nachmias VT (March 1991). "Thymosin beta 4 and Fx, an actin-sequestering peptide, are indistinguishable". J. Biol. Chem. 266 (7): 4029–32. PMID 1999398.
12. Lodish, Harvey F. (2000). "Chapter 18. Cell Motility and Shape I: Microfilaments. 18.2. The Dynamics of Actin Assembly". Molecular cell biology. San Francisco: W.H. Freeman. ISBN 978-0-7167-3706-3.
13. Xue B, Aguda AH, Robinson RC (September 2007). "Models of the actin-bound forms of the beta-thymosins". Annals of the New York Academy of Sciences. 1112 (1): 56–66. Bibcode:2007NYASA1112...56X. doi:10.1196/annals.1415.010. PMID 17468228.
14. Jeffery CJ (January 1999). "Moonlighting proteins". Trends Biochem. Sci. 24 (1): 8–11. doi:10.1016/S0968-0004(98)01335-8. PMID 10087914.
15. Tompa P, Szász C, Buday L (September 2005). "Structural disorder throws new light on moonlighting". Trends Biochem. Sci. 30 (9): 484–9. doi:10.1016/j.tibs.2005.07.008. PMID 16054818.
16. Freeman KW, Bowman BR, Zetter BR (November 2010). "Regenerative protein thymosin {beta}-4 is a novel regulator of purinergic signaling". FASEB J. 25 (3): 907–15. doi:10.1096/fj.10-169417. PMID 21106936.
17. Philp D, Kleinman HK (April 2010). "Animal studies with thymosin beta, a multifunctional tissue repair and regeneration peptide". Annals of the New York Academy of Sciences. 1194 (1): 81–6. Bibcode:2010NYASA1194...81P. doi:10.1111/j.1749-6632.2010.05479.x. PMID 20536453.
18. Smart N, Bollini S, Dubé KN, Vieira JM, Zhou B, Davidson S, Yellon D, Riegler J, Price AN, Lythgoe MF, Pu WT, Riley PR (June 2011). "De novo cardiomyocytes from within the activated adult heart after injury". Nature. 474 (7353): 640–4. doi:10.1038/nature10188. PMC 3696525. PMID 21654746. Lay summary – BBC News.
19. Smart N, Riley PR (February 2009). Derivation of epicardium-derived progenitor cells (EPDCs) from adult epicardium. Curr Protoc Stem Cell Biol. Chapter 2. pp. Unit2C.2. doi:10.1002/9780470151808.sc02c02s8. ISBN 978-0470151808. PMID 19235142.
20. Riley PR, Smart N (December 2009). "Thymosin beta4 induces epicardium-derived neovascularization in the adult heart". Biochem. Soc. Trans. 37 (Pt 6): 1218–20. doi:10.1042/BST0371218. PMID 19909250.
21. Young JD, Lawrence AJ, MacLean AG, Leung BP, McInnes IB, Canas B, Pappin DJ, Stevenson RD (December 1999). "Thymosin beta 4 sulfoxide is an anti-inflammatory agent generated by monocytes in the presence of glucocorticoids". Nature Medicine. 5 (12): 1424–7. doi:10.1038/71002. PMID 10581087.
22. Crockford D, Turjman N, Allan C, Angel J (April 2010). "Thymosin beta4: structure, function, and biological properties supporting current and future clinical applications". Annals of the New York Academy of Sciences. 1194 (1): 179–89. Bibcode:2010NYASA1194..179C. doi:10.1111/j.1749-6632.2010.05492.x. PMID 20536467.
23. Kleinman HK, Sosne G (2016). Thymosin β4 Promotes Dermal Healing. review. Vitamins and Hormones. 102. pp. 251–75. doi:10.1016/bs.vh.2016.04.005. ISBN 9780128048184. PMID 27450738.
24. Sosne G, Kleinman HK (August 2015). "Primary Mechanisms of Thymosin β4 Repair Activity in Dry Eye Disorders and Other Tissue Injuries". Investigative Ophthalmology & Visual Science. 56 (9): 5110–7. doi:10.1167/iovs.15-16890. PMID 26241398.
25. Koh B. "Cronulla Sharks and thymosin beta-4 … is it doping?". The Conversation.
26. Ho EN, Kwok WH, Lau MY, Wong AS, Wan TS, Lam KK, Schiff PJ, Stewart BD (Nov 2012). "Doping control analysis of TB-500, a synthetic version of an active region of thymosin β₄, in equine urine and plasma by liquid chromatography-mass spectrometry". Journal of Chromatography A. 1265: 57–69. doi:10.1016/j.chroma.2012.09.043. PMID 23084823.
27. "Essendon supplements saga: ASADA backs Court of Arbitration for Sport decision to upheld WADA appeal". ABC News (Australian Broadcasting Corporation).
28. Ballweber E, Hannappel E, Huff T, Stephan H, Haener M, Taschner N, Stoffler D, Aebi U, Mannherz HG (Jan 2002). "Polymerisation of chemically cross-linked actin:thymosin beta(4) complex to filamentous actin: alteration in helical parameters and visualisation of thymosin beta(4) binding on F-actin". Journal of Molecular Biology. 315 (4): 613–25. doi:10.1006/jmbi.2001.5281. PMID 11812134.
29. Safer D, Sosnick TR, Elzinga M (May 1997). "Thymosin beta 4 binds actin in an extended conformation and contacts both the barbed and pointed ends". Biochemistry. 36 (19): 5806–16. doi:10.1021/bi970185v. PMID 9153421.
30. Hertzog M, van Heijenoort C, Didry D, Gaudier M, Coutant J, Gigant B, Didelot G, Préat T, Knossow M, Guittet E, Carlier MF (May 2004). "The beta-thymosin/WH2 domain; structural basis for the switch from inhibition to promotion of actin assembly". Cell. 117 (5): 611–23. doi:10.1016/S0092-8674(04)00403-9. PMID 15163409.
31. Van Troys M, Dewitte D, Goethals M, Carlier MF, Vandekerckhove J, Ampe C (Jan 1996). "The actin binding site of thymosin beta 4 mapped by mutational analysis". The EMBO Journal. 15 (2): 201–10. doi:10.1002/j.1460-2075.1996.tb00350.x. PMC 449934. PMID 8617195.

Further reading

• Huff T, Müller CS, Otto AM, Netzker R, Hannappel E (Mar 2001). "beta-Thymosins, small acidic peptides with multiple functions". The International Journal of Biochemistry & Cell Biology. 33 (3): 205–20. doi:10.1016/S1357-2725(00)00087-X. PMID 11311852.
• Bubb MR (2003). Thymosin beta 4 interactions. Vitamins & Hormones. 66. pp. 297–316. doi:10.1016/S0083-6729(03)01008-2. ISBN 9780127098661. PMID 12852258.
• Goldschmidt-Clermont PJ, Furman MI, Wachsstock D, Safer D, Nachmias VT, Pollard TD (Sep 1992). "The control of actin nucleotide exchange by thymosin beta 4 and profilin. A potential regulatory mechanism for actin polymerization in cells". Molecular Biology of the Cell. 3 (9): 1015–24. doi:10.1091/mbc.3.9.1015. PMC 275662. PMID 1330091.
• Sanders MC, Goldstein AL, Wang YL (May 1992). "Thymosin beta 4 (Fx peptide) is a potent regulator of actin polymerization in living cells". Proceedings of the National Academy of Sciences of the United States of America. 89 (10): 4678–82. Bibcode:1992PNAS...89.4678S. doi:10.1073/pnas.89.10.4678. PMC 49146. PMID 1584803.
• Safer D, Elzinga M, Nachmias VT (Mar 1991). "Thymosin beta 4 and Fx, an actin-sequestering peptide, are indistinguishable". The Journal of Biological Chemistry. 266 (7): 4029–32. PMID 1999398.
• Clauss IM, Wathelet MG, Szpirer J, Islam MQ, Levan G, Szpirer C, Huez GA (Jan 1991). "Human thymosin-beta 4/6-26 gene is part of a multigene family composed of seven members located on seven different chromosomes". Genomics. 9 (1): 174–80. doi:10.1016/0888-7543(91)90236-8. PMID 2004759.
• Soma G, Murata M, Kitahara N, Gatanaga T, Shibai H, Morioka H, Andoh T (Oct 1985). "Detection of a countertranscript in promyelocytic leukemia cells HL60 during early differentiation by TPA". Biochemical and Biophysical Research Communications. 132 (1): 100–9. doi:10.1016/0006-291X(85)90994-5. PMID 2998351.
• Gondo H, Kudo J, White JW, Barr C, Selvanayagam P, Saunders GF (Dec 1987). "Differential expression of the human thymosin-beta 4 gene in lymphocytes, macrophages, and granulocytes". Journal of Immunology. 139 (11): 3840–8. PMID 3500230.
• Friedman RL, Manly SP, McMahon M, Kerr IM, Stark GR (Oct 1984). "Transcriptional and posttranscriptional regulation of interferon-induced gene expression in human cells". Cell. 38 (3): 745–55. doi:10.1016/0092-8674(84)90270-8. PMID 6548414.
• Erickson-Viitanen S, Ruggieri S, Natalini P, Horecker BL (Mar 1983). "Distribution of thymosin beta 4 in vertebrate classes". Archives of Biochemistry and Biophysics. 221 (2): 570–6. doi:10.1016/0003-9861(83)90177-7. PMID 6838210.
• Pantaloni D, Carlier MF (Dec 1993). "How profilin promotes actin filament assembly in the presence of thymosin beta 4". Cell. 75 (5): 1007–14. doi:10.1016/0092-8674(93)90544-Z. PMID 8252614.
• Van Troys M, Dewitte D, Goethals M, Carlier MF, Vandekerckhove J, Ampe C (Jan 1996). "The actin binding site of thymosin beta 4 mapped by mutational analysis". The EMBO Journal. 15 (2): 201–10. doi:10.1002/j.1460-2075.1996.tb00350.x. PMC 449934. PMID 8617195.
• Feinberg J, Heitz F, Benyamin Y, Roustan C (May 1996). "The N-terminal sequences (5-20) of thymosin beta 4 binds to monomeric actin in an alpha-helical conformation". Biochemical and Biophysical Research Communications. 222 (1): 127–32. doi:10.1006/bbrc.1996.0709. PMID 8630056.
• Safer D, Sosnick TR, Elzinga M (May 1997). "Thymosin beta 4 binds actin in an extended conformation and contacts both the barbed and pointed ends". Biochemistry. 36 (19): 5806–16. doi:10.1021/bi970185v. PMID 9153421.
• Malinda KM, Goldstein AL, Kleinman HK (May 1997). "Thymosin beta 4 stimulates directional migration of human umbilical vein endothelial cells". FASEB Journal. 11 (6): 474–81. doi:10.1096/fasebj.11.6.9194528. PMID 9194528.
• Chen J, Peterson RT, Schreiber SL (Jun 1998). "Alpha 4 associates with protein phosphatases 2A, 4, and 6". Biochemical and Biophysical Research Communications. 247 (3): 827–32. doi:10.1006/bbrc.1998.8792. PMID 9647778.
• Huff T, Ballweber E, Humeny A, Bonk T, Becker C, Müller CS, Mannherz HG, Hannappel E (Dec 1999). "Thymosin beta(4) serves as a glutaminyl substrate of transglutaminase. Labeling with fluorescent dansylcadaverine does not abolish interaction with G-actin". FEBS Letters. 464 (1–2): 14–20. doi:10.1016/S0014-5793(99)01670-1. PMID 10611475.
• De La Cruz EM, Ostap EM, Brundage RA, Reddy KS, Sweeney HL, Safer D (May 2000). "Thymosin-beta(4) changes the conformation and dynamics of actin monomers". Biophysical Journal. 78 (5): 2516–27. Bibcode:2000BpJ....78.2516D. doi:10.1016/S0006-3495(00)76797-X. PMC 1300842. PMID 10777749.