Preview

Russian journal of neurosurgery

Advanced search

Materials based on spider silk for regenerative medicine

https://doi.org/10.63769/1683-3295-2026-28-2-113-121

Abstract

Spider silk is an unusually strong, flexible, biocompatible natural biomaterial that is becoming attractive for scientific research with the possibility of translation into clinical practice. Female orb-weaving spiders of the genus Nephila clavipes produce up to seven different types of silk, using various silk glands and spinning organs located at the posterior end of the spider’s abdomen. The main proteins are the main ampulla spidroins MaSp1 and MaSp2, which can be used to create recombinant spider silk due to the limitation of web collection in vivo. The review highlights studies dedicated to the use of spider silk-based materials in the field of tissue engineering in vitro. In particular, data on the use of two-dimensional and three-dimensional models and scaffolds for tissue engineering with the possibility of using modern technologies such as bioprinting are summarized. 

About the Authors

S. V. Piatnitskaia
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

Svetlana Viktorovna Piatnitskaia  

3 Lenina St., Ufa 450008 



Sh. M. Safin
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



R. A. Zamanova
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



A. I. Fairushina
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



D. Z. Makhyanov
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



N. I. Abdullina
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



G. R. Kireeva
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



I. F. Faskhutdinov
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



V. A. Smirnov
Sklifosovsky Research Institute for Emergency Medicine, Moscow Healthcare Department
Russian Federation

3 Bolshaya Sukharevskaya Ploshchad, Moscow 129090 



V. V. Krylov
Sklifosovsky Research Institute for Emergency Medicine, Moscow Healthcare Department; Russian Center of Neurology and Neuroscience; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia
Russian Federation

3 Bolshaya Sukharevskaya Ploshchad, Moscow 129090 

80 Volokolamskoye Shosse, Moscow 125367 

1 Ostrovityanova St., Moscow 117513 



V. N. Pavlov
Bashkir State Medical University, Ministry of Health of Russia
Russian Federation

3 Lenina St., Ufa 450008 



References

1. Vincent J.F., Bogatyreva O.A., Bogatyrev N.R. et al. Biomimetics: its practice and theory. J R Soc Interface 2006;3(9):471–82. DOI: 10.1098/rsif.2006.0127

2. Oladele I.O., Onuh L., Taiwo A.S. et al. Mechanical, wear and thermal conductivity characteristics of snail shell-derived hydroxyapatite reinforced epoxy bio-composites for adhesive biomaterials applications. Int J Sustain  Eng 2022;15(1):122–35.

3. Li H., Hu C., Yu H., Chen C. Chitosan composite scaffolds for articular cartilage defect repair: a review. RSC Adv 2018;8(7):3736–49. DOI: 10.1039/c7ra11593h

4. Rogina A., Pušić M., Štefan L. et al. Characterization of chitosanbased scaffolds seeded with sheep nasal chondrocytes for cartilage tissue engineering. Ann Biomed Eng 2021;49(6):1572–86. DOI: 10.1007/s10439-020-02712-9

5. Che X., Zhao T., Hu J. et al. Application of chitosan-based hydrogel in promoting wound healing: a review. Polymers (Basel) 2024;16(3):344. DOI: 10.3390/polym16030344

6. Liu H., Lv P., Zhu Y. et al. Salidroside promotes peripheral nerve regeneration based on tissue engineering strategy using Schwann cells and PLGA: in vitro and in vivo. Sci Rep 2017;7:39869. DOI: 10.1038/srep39869

7. Allmeling C., Jokuszies A., Reimers K. et al. Spider silk fibres in artificial nerve constructs promote peripheral nerve regeneration. Cell Prolif 2008;41(3):408–20. DOI: 10.1111/j.1365-2184.2008.00534.x

8. Allmeling C., Jokuszies A., Reimers K. et al. Use of spider silk fibres as an innovative material in a biocompatible artificial nerve conduit. J Cell Mol Med 2006;10(3):770–7. DOI: 10.1111/j.1582-4934.2006.tb00436.x

9. Rising A., Johansson J. Toward spinning artificial spider silk. Nat Chem Biol 2015;11(5):309–15. DOI: 10.1038/nchembio.1789

10. Babb P.L., Lahens N.F., Correa-Garhwal S.M. et al. The Nephila clavipes genome highlights the diversity of spider silk genes and their complex expression. Nat Genet 2017;49(6):895–903. DOI: 10.1038/ng.3852

11. Kluge J.A., Rabotyagova O., Leisk G.G., Kaplan D.L. Spider silks and their applications. Trends Biotechnol 2008;26(5):244–51. DOI: 10.1016/j.tibtech.2008.02.006

12. Shanafelt M., Larracas C., Dyrness S. et al. Egg case protein 3: a constituent of black widow spider tubuliform silk. Molecules 2021;26(16):5088. DOI: 10.3390/molecules26165088

13. Peakall D.B. Synthesis of silk, mechanism and location. Am Zool 1969;9(1):71–9.

14. Arndt T., Jaudzems K., Shilkova O. et al. Spidroin  N-terminal domain forms amyloid-like fibril based hydrogels and provides a protein immobilization platform. Nat Commun 2022;13(1):4695. DOI: 10.1038/s41467-022-32093-7

15. Collin M.A., Clarke T.H. 3rd, Ayoub N.A., Hayashi C.Y. Genomic perspectives of spider silk genes through target capture sequencing: conservation of stabilization mechanisms and homology-based structural models of spidroin terminal regions. Int J Biol Macromol 2018;113:829–40. DOI: 10.1016/j.ijbiomac.2018.02.032

16. Garb J.E., Haney R.A., Schwager E.E. et al. The transcriptome of Darwin’s bark spider silk glands predicts proteins contributing to dragline silk toughness. Commun Biol 2019;2:275. DOI: 10.1038/s42003-019-0496-1

17. Saric M., Eisoldt L., Döring V., Scheibel T. Interplay of different major ampullate spidroins during assembly and implications for fiber mechanics. Adv Mater 2021;33(9). DOI: 10.1002/adma.202006499

18. Arakawa K., Kono N., Malay A.D. et al. 1000 spider silkomes: linking sequences to silk physical properties. Sci Adv 2022;8(41). DOI: 10.1126/sciadv.abo6043

19. Li J., Li S., Huang J. et al. Spider silk-inspired artificial fibers. Adv Sci (Weinh) 2022;9(5). DOI: 10.1002/advs.202103965

20. Ramezaniaghdam M., Nahdi N.D., Reski R. Recombinant spider silk: promises and bottlenecks. Front Bioeng Biotechnol 2022;10:835637. DOI: 10.3389/fbioe.2022.835637

21. Agnarsson I., Kuntner M., Blackledge T.A. Bioprospecting finds the toughest biological material: extraordinary silk from a giant riverine orb spider. PLoS One 2010;5(9):e11234. DOI: 10.1371/journal.pone.0011234

22. Liu R., Deng Q., Yang Z. et al. “Nano-fishnet” structure making silk fibers tougher. Adv Funct Mater 2016;26(33):5534–41. DOI: 10.1002/adfm.201600813

23. Yazawa K., Malay A.D., Masunaga H., Numata K. Role of skin layers on mechanical properties and supercontraction of spider dragline silk fiber. Macromol Biosci 2019;19(3):e1800220. DOI: 10.1002/mabi.201800220

24. Du N., Yang Z., Liu X.Y. et al. Structural origin of the strainhardening of spider silk. Adv Funct Mater 2011;21(5):772–8. DOI: 10.1002/adfm.201001397

25. Vollrath F., Madsen B., Shao Z. The effect of spinning conditions on the mechanics of a spider’s dragline silk. Proc Biol Sci 2001;268(1483):2339–46. DOI: 10.1098/rspb.2001.1590

26. Lefèvre T., Boudreault S., Cloutier C., Pézolet M. Diversity of molecular transformations involved in the formation of spider silks. J Mol Biol 2011;405(1):238–53. DOI: 10.1016/j.jmb.2010.10.052

27. Liu Y., Shao Z., Vollrath F. Elasticity of spider silks. Biomacromolecules 2008;9(7):1782–6. DOI: 10.1021/bm7014174

28. Giesa T., Schuetz R., Fratzl P. et al. Unraveling the molecular requirements for macroscopic silk supercontraction. ACS Nano 2017;11(10):9750–8. DOI: 10.1021/acsnano.7b01532

29. Lee S.M., Pippel E., Moutanabbir O. et al. In situ Raman spectroscopic study of  Al-infiltrated spider dragline silk under tensile deformation. ACS Appl Mater Interfaces 2014;6(19): 16827–34. DOI: 10.1021/am5041797

30. Gobbi S.J., Gobbi V.J., Rocha Y. Requirements for selection/ development of a biomaterial. Biomed J Sci Tech Res 2019;14(3). DOI: 10.26717/BJSTR.2019.14.002554

31. Kiradzhiyska D.D., Mantcheva R.D. Overview of biocompatible materials and their use in medicine. Folia Med (Plovdiv) 2019;61(1):34–40. DOI: 10.2478/folmed-2018-0038

32. Zeplin P.H., Maksimovikj N.C., Jordan M.C. et al. Spider silk coatings as a bioshield to reduce periprosthetic fibrous capsule formation. Adv Funct Mater 2014;24(17):2658–66. DOI: 10.1002/adfm.201302813

33. Kuhbier J.W., Coger V., Mueller J. et al. Influence of direct or indirect contact for the cytotoxicity and blood compatibility of spider silk. J Mater Sci Mater Med 2017;28(8):127. DOI: 10.1007/s10856-017-5936-1

34. Keiser C.N., DeMarco A.E., Shearer T.A. et al. Putative microbial defenses in a social spider: immune variation and antibacterial properties of colony silk. J Arachnol 2015;43(3):394–9. DOI: 10.1636/arac-43-03-394-399

35. Tahir H.M., Qamar S., Sattar A. et al. Evidence for the antimicrobial potential of silk of Cyclosa confraga (Thorell, 1892) (Araneae: Araneidae). Acta Zool Bulg 2017;69:593–5.

36. Esteves F.G., Dos Santos-Pinto J.R.A., Ferro M. et al. Revealing the venomous secrets of the spider’s web. J Proteome Res 2020;19(8):3044–59. DOI: 10.1021/acs.jproteome.0c00086

37. Babczyńska A., Sułowicz S., Talik E. et al. Sterile capsule-egg cocoon covering constitutes an antibacterial barrier for spider parasteatoda tepidariorum embryos. Physiol Biochem Zool 2019;92(1):115–24. DOI: 10.1086/701390

38. Makover V., Ronen Z., Lubin Y., Khalaila I. Eggshell spheres protect brown widow spider (Latrodectus geometricus) eggs from bacterial infection. J R Soc Interface 2019;16(150):20180581. DOI: 10.1098/rsif.2018.0581

39. Haq I.U., Qasim M., Rahim K. et al. Efficacy of the spider web metabolites activity against multi-drug resistant (MDR) bacteria. Appl Ecol Environ Res 2019;17(5):10899–908. DOI: 10.15666/aeer/1705_1089910908

40. Fruergaard S., Lund M.B., Schramm A. et al. The myth of antibiotic spider silk. iScience 2021;24(10):103125. DOI: 10.1016/j.isci.2021.103125

41. Wright S., Goodacre S.L. Evidence for antimicrobial activity associated with common house spider silk. BMC Res Notes 2012;5:326. DOI: 10.1186/1756-0500-5-326

42. Agapova O.I. Silk fibroin and spidroin bioengineering constructions for regenerative medicine and tissue engineering (review). Sovremennye tehnologii v medicine = Modern Technologies in Medicine 2017;9(2):190–206. (In  Russ.). DOI: 10.17691/stm2017.9.2.24

43. Debabov V.G., Bogush V.G. Recombinant spidroins as the basis for new materials. ACS Biomater Sci Eng 2020;6(7):3745–61. DOI: 10.1021/acsbiomaterials.0c00109

44. Kretov E.I., Zapolotsky E.N., Tarkova A.R. et al. Electrospinning for the design of medical supplies. Byulleten sibirskoy meditsiny = Bulletin of  Siberian Medicine 2020;(2):153–62. (In  Russ.). DOI: 10.20538/1682-0363-2020-2-153-162

45. Mikhailova M.M., Sydoruk K.V., Davydova L.I. et al. Nonwoven spidroin materials as scaffolds for ex vivo cultivation of aortic fragments and dorsal root ganglia. J Biomater Sci Polym Ed 2022;33(13):1685–703. DOI: 10.1080/09205063.2022.2073426

46. Kuhbier J.W., Allmeling C., Reimers K. et al. Interactions between spider silk and cells – NIH/3T3 fibroblasts seeded on miniature weaving frames. PLoS One 2010;5(8):e12032. DOI: 10.1371/journal.pone.0012032

47. Kuhbier J.W., Reimers K., Kasper C. et al. First investigation of spider silk as a braided microsurgical suture. J Biomed Mater Res B Appl Biomater 2011;97(2):381–7. DOI: 10.1002/jbm.b.31825

48. Strauß S., Diemer M., Bucan V. et al. Spider silk enhanced tissue engineering of cartilage tissue: approach of a novel bioreactor model using adipose derived stromal cells. J Appl Biomater Funct Mater 2024;22. DOI: 10.1177/22808000241226656

49. Steins A., Dik P., Müller W.H. et al. In vitro evaluation of spider silk meshes as a potential biomaterial for bladder reconstruction. PLoS One 2015;10(12):e0145240. DOI: 10.1371/journal.pone.0145240

50. Malyugin B.E., Borzenok S.A., Saburina I.N. et al. Development of a bioengineered artificial cornea based on a spidroin film matrix and cultured limbal cells. Oftal’mokhirurgiya = Ophthalmic Surgery 2013;(4):89–97. (In  Russ.).

51. Malyugin B.E., Borzenok S.A., Komakh Yu.A. et al. Modern possibilities of cellular technologies in the construction of a biological equivalent of an artificial cornea. Sibirskiy nauchnyy meditsinskiy zhurnal = Siberian Scientific Medical Journal 2014;(5). (In  Russ.).

52. Agapova O.I., Efimov A.E., Moisenovich M.M. et al. Comparative analysis of three-dimensional nanostructure of porous biocompatible scaffolds made of recombinant spidroin and silk fibroin for regenerative medicine. Vestnik transplantologii i iskusstvennykh organov = Russian Journal of Transplantology and  Artificial Organs 2015;17(2):37–44. (In  Russ.). DOI: 10.15825/1995-1191-2015-2-37-44

53. Agapova O.I., Druzhinina T.V., Trofimov K.V. et al. Biodegradable porous matrices for bone tissue regeneration. Perspektivnye materialy = Promising Materials 2015;(8):17–26. (In  Russ.).

54. Mehta N., Hede S. Spider silk calcite composite. Hypothesis 2005;3(2):21.

55. Dmitrović S. Synthesis and characterization of spider silk calcite composite. Proces Appl Ceram 2016;10(1):37–40.

56. Cao B., Mao C. Oriented nucleation of hydroxylapatite crystals on spider dragline silks. Langmuir 2007;23(21):10701–5. DOI: 10.1021/la7014435

57. Sun Y., Jia X., Meng Q. Characteristic evaluation of recombinant MiSp/Poly(lactic-co-glycolic) Acid (PLGA) nanofiber scaffolds as potential scaffolds for bone tissue engineering. Int J Mol Sci 2023;24(2):1219. DOI: 10.3390/ijms24021219

58. Tasiopoulos C.P., Petronis S., Sahlin  H., Hedhammar M. Surface functionalization of PTFE membranes intended for guided bone regeneration using recombinant spider silk. ACS Appl Bio Mater 2020;3(1):577–83. DOI: 10.1021/acsabm.9b00972

59. Freeman S., Calabro S., Williams R. et al. Bioink formulation and machine learning-empowered bioprinting optimization. Front Bioeng Biotechnol 2022;10:913579. DOI: 10.3389/fbioe.2022.913579

60. Fu Z., Naghieh S., Xu C. et al. Printability in extrusion bioprinting. Biofabrication 2021;13(3). DOI: 10.1088/1758-5090/abe7ab

61. Gao T., Gillispie G.J., Copus J.S. et al. Optimization of gelatinalginate composite bioink printability using rheological parameters: a systematic approach. Biofabrication 2018;10(3):034106. DOI: 10.1088/1758-5090/aacdc7

62. Contessi Negrini N., Celikkin  N., Tarsini P. et al. Threedimensional printing of chemically crosslinked gelatin hydrogels for adipose tissue engineering. Biofabrication 2020;12(2):025001. DOI: 10.1088/1758-5090/ab56f9

63. Petta D., D’Amora U., Ambrosio L. et al. Hyaluronic acid as a bioink for extrusion-based 3D printing. Biofabrication 2020;12(3):032001. DOI: 10.1088/1758-5090/ab8752

64. Stepanovska J., Supova M., Hanzalek K. et al. Collagen bioinks for bioprinting: a systematic review of hydrogel properties, bioprinting parameters, protocols, and bioprinted structure characteristics. Biomedicines 2021;9(9):1137. DOI: 10.3390/biomedicines9091137

65. Magli S., Rossi G.B., Risi G. et al. Design and synthesis of chitosan-gelatin hybrid hydrogels for 3D Printable in vitro models. Front Chem 2020;8:524. DOI: 10.3389/fchem.2020.00524

66. Sun Y., Ku B.J., Moon M.J. Microstructure of the silk fibroin-based hydrogel scaffolds derived from the orb-web spider Trichonephila clavata. Appl Microsc 2024;54(3). DOI: 10.1186/s42649-024-00096-x

67. Lechner A., Trossmann V.T., Scheibel T. Impact of cell loading of recombinant spider silk based bioinks on gelation and printability. Macromol Biosci 2022;22(3). DOI: 10.1002/mabi.202100390


Review

For citations:


Piatnitskaia S.V., Safin Sh.M., Zamanova R.A., Fairushina A.I., Makhyanov D.Z., Abdullina N.I., Kireeva G.R., Faskhutdinov I.F., Smirnov V.A., Krylov V.V., Pavlov V.N. Materials based on spider silk for regenerative medicine. Russian journal of neurosurgery. 2026;28(2):113-121. (In Russ.) https://doi.org/10.63769/1683-3295-2026-28-2-113-121

Views: 73

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1683-3295 (Print)
ISSN 2587-7569 (Online)
X