Analyze Diet
BioMed research international2015; 2015; 141485; doi: 10.1155/2015/141485

Immunomodulatory Role of Adipose-Derived Stem Cells on Equine Endometriosis.

Abstract: Endometriosis is a degenerative process due to a chronic inflammatory damage leading to extracellular matrix components deposition and glandular fibrosis. It is known that mesenchymal stem cells secrete a wide range of bioactive molecules, some of them modulating the immune inflammatory response, and others providing regeneration and remodeling of injured tissue. We have performed in vitro experiments in order to analyze the capability of allogenic equine adipose-derived stem cells (ADSCs) to infiltrate mares' endometrial tissues and to stimulate the expression of cytokines and metallopeptidases. Differences in the biologic response to the exposure to ADSCs between pathological and healthy endometrial tissue have been identified. These results could challenge researchers to progress forward with future studies for the development of a biological therapy with a possible application in translational medicine.
Publication Date: 2015-06-09 PubMed ID: 26180781PubMed Central: PMC4477049DOI: 10.1155/2015/141485Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research article investigates the potential of equine adipose-derived stem cells (ADSCs) in modulating the immune inflammatory response and damage in endometriosis in horses. It provides insight into how ADSCs can affect the expression of cytokines and metalloproteinases, indicating potential for a biological treatment approach.

Research context and objectives

  • The study centers on endometriosis, a degenerative condition associated with chronic inflammatory damage. It results in the deposition of extracellular matrix components and glandular fibrosis.
  • Mesenchymal stem cells, which have been known to secrete a variety of bioactive molecules, were the focus of this study. Some of these molecules can modulate the immune inflammatory response, while others promote the regeneration and remodeling of damaged tissue.
  • The primary objective of the research was to examine the capacity of equine adipose-derived stem cells (ADSCs) to infiltrate the endometrial tissues of mares and stimulate the expression of cytokines and metallopeptidases.

Methods and findings

  • The research team performed in vitro experiments, working directly with cells and tissues outside their normal biological context.
  • They found that the exposure to ADSCs triggered different biological responses between healthy and pathological (diseased) endometrial tissue. This suggests that ADSCs have particular ways of interacting with disease processes in the endometrium.
  • Although the research was conducted on horses, its findings have potential implications for understanding and treating endometriosis in other mammals, including humans.

Conclusion and future implications

  • These findings provide a new perspective on the role of ADSCs in treating endometriosis. It suggests that these cells can influence the immune inflammatory response and tissue recovery in the endometrium.
  • Future studies are likely to expand on these findings and pursue the development of a biological treatment for endometriosis based on the application of ADSCs.
  • This has the potential to contribute significantly to translational medicine, the field that aims to “translate” findings in fundamental research into medical practice and meaningful health outcomes.

Cite This Article

APA
Falomo ME, Ferroni L, Tocco I, Gardin C, Zavan B. (2015). Immunomodulatory Role of Adipose-Derived Stem Cells on Equine Endometriosis. Biomed Res Int, 2015, 141485. https://doi.org/10.1155/2015/141485

Publication

ISSN: 2314-6141
NlmUniqueID: 101600173
Country: United States
Language: English
Volume: 2015
Pages: 141485
PII: 141485

Researcher Affiliations

Falomo, Maria Elena
  • Department of Veterinary Clinical Sciences, Viale dell'Università 16, 35100 Padua, Italy.
Ferroni, Letizia
  • Department of Biomedical Sciences, University of Padua, Via G. Colombo 3, 35100 Padua, Italy.
Tocco, Ilaria
  • Department of Neurosciences, University of Padua, Via Giustiniani 2, 35100 Padua, Italy.
Gardin, Chiara
  • Department of Biomedical Sciences, University of Padua, Via G. Colombo 3, 35100 Padua, Italy.
Zavan, Barbara
  • Department of Biomedical Sciences, University of Padua, Via G. Colombo 3, 35100 Padua, Italy.

MeSH Terms

  • Adipose Tissue / immunology
  • Allografts
  • Animals
  • Cytokines / immunology
  • Endometriosis / immunology
  • Endometriosis / therapy
  • Endometriosis / veterinary
  • Female
  • Gelatinases / immunology
  • Horse Diseases / immunology
  • Horse Diseases / therapy
  • Horses
  • Mesenchymal Stem Cell Transplantation
  • Mesenchymal Stem Cells / immunology

References

This article includes 31 references
  1. Carrade DD, Lame MW, Kent MS, Clark KC, Walker NJ, Borjesson DL. Comparative Analysis of the Immunomodulatory Properties of Equine Adult-Derived Mesenchymal Stem Cells().. Cell Med 2012;4(1):1-11.
    pmc: PMC3495591pubmed: 23152950doi: 10.3727/215517912x647217google scholar: lookup
  2. Di Nicola M, Carlo-Stella C, Magni M, Milanesi M, Longoni PD, Matteucci P, Grisanti S, Gianni AM. Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli.. Blood 2002 May 15;99(10):3838-43.
    doi: 10.1182/blood.v99.10.3838pubmed: 11986244google scholar: lookup
  3. Krampera M, Glennie S, Dyson J, Scott D, Laylor R, Simpson E, Dazzi F. Bone marrow mesenchymal stem cells inhibit the response of naive and memory antigen-specific T cells to their cognate peptide.. Blood 2003 May 1;101(9):3722-9.
    doi: 10.1182/blood-2002-07-2104pubmed: 12506037google scholar: lookup
  4. Comoli P, Ginevri F, Maccario R, Avanzini MA, Marconi M, Groff A, Cometa A, Cioni M, Porretti L, Barberi W, Frassoni F, Locatelli F. Human mesenchymal stem cells inhibit antibody production induced in vitro by allostimulation.. Nephrol Dial Transplant 2008 Apr;23(4):1196-202.
    doi: 10.1093/ndt/gfm740pubmed: 18029377google scholar: lookup
  5. Nauta AJ, Kruisselbrink AB, Lurvink E, Willemze R, Fibbe WE. Mesenchymal stem cells inhibit generation and function of both CD34+-derived and monocyte-derived dendritic cells.. J Immunol 2006 Aug 15;177(4):2080-7.
    doi: 10.4049/jimmunol.177.4.2080pubmed: 16887966google scholar: lookup
  6. Gonzalez-Rey E, Anderson P, González MA, Rico L, Büscher D, Delgado M. Human adult stem cells derived from adipose tissue protect against experimental colitis and sepsis.. Gut 2009 Jul;58(7):929-39.
    doi: 10.1136/gut.2008.168534pubmed: 19136511google scholar: lookup
  7. Parekkadan B, Tilles AW, Yarmush ML. Bone marrow-derived mesenchymal stem cells ameliorate autoimmune enteropathy independently of regulatory T cells.. Stem Cells 2008 Jul;26(7):1913-9.
    doi: 10.1634/stemcells.2007-0790pubmed: 18420833google scholar: lookup
  8. Benvenuto F, Ferrari S, Gerdoni E, Gualandi F, Frassoni F, Pistoia V, Mancardi G, Uccelli A. Human mesenchymal stem cells promote survival of T cells in a quiescent state.. Stem Cells 2007 Jul;25(7):1753-60.
    doi: 10.1634/stemcells.2007-0068pubmed: 17395776google scholar: lookup
  9. Crop MJ, Baan CC, Korevaar SS, Ijzermans JN, Weimar W, Hoogduijn MJ. Human adipose tissue-derived mesenchymal stem cells induce explosive T-cell proliferation.. Stem Cells Dev 2010 Dec;19(12):1843-53.
    doi: 10.1089/scd.2009.0368pubmed: 20367242google scholar: lookup
  10. Mambelli LI, Winter GH, Kerkis A, Malschitzky E, Mattos RC, Kerkis I. A novel strategy of mesenchymal stem cells delivery in the uterus of mares with endometrosis.. Theriogenology 2013 Mar 15;79(5):744-50.
  11. Hoffmann C, Ellenberger C, Mattos RC, Aupperle H, Dhein S, Stief B, Schoon HA. The equine endometrosis: new insights into the pathogenesis.. Anim Reprod Sci 2009 Apr;111(2-4):261-78.
  12. Aresu L, Benali S, Giannuzzi D, Mantovani R, Castagnaro M, Falomo ME. The role of inflammation and matrix metalloproteinases in equine endometriosis.. J Vet Sci 2012 Jun;13(2):171-7.
    doi: 10.4142/jvs.2012.13.2.171pmc: PMC3386342pubmed: 22705739google scholar: lookup
  13. Fiala SM, Pimentel CA, Gregory RM, Mattos RC. Does equine sperm concentration influence the sperm migration to the oviducts?. Anim Reprod Sci 2005 Oct;89(1-4):261-4.
    pubmed: 16265735
  14. Fiala SM, Pimentel CA, Mattos AL, Gregory RM, Mattos RC. Effect of sperm numbers and concentration on sperm transport and uterine inflammatory response in the mare.. Theriogenology 2007 Feb;67(3):556-62.
  15. Cadario ME, Thatcher WW, Klapstein E, Merrit AM, Archbald LF, Thatcher MJ, LeBlanc MM. Dynamics of prostaglandin secretion, intrauterine fluid and uterine clearance in reproductively normal mares and mares with delayed uterine clearance.. Theriogenology 1999 Nov;52(7):1181-92.
    doi: 10.1016/S0093-691X(99)00210-1pubmed: 10735096google scholar: lookup
  16. Troedsson MH. Uterine clearance and resistance to persistent endometritis in the mare.. Theriogenology 1999 Aug;52(3):461-71.
    doi: 10.1016/S0093-691X(99)00143-0pubmed: 10734380google scholar: lookup
  17. Woodward EM, Christoffersen M, Campos J, Betancourt A, Horohov D, Scoggin KE, Squires EL, Troedsson MH. Endometrial inflammatory markers of the early immune response in mares susceptible or resistant to persistent breeding-induced endometritis.. Reproduction 2013 Mar 1;145(3):289-96.
    doi: 10.1530/rep-12-0452pubmed: 23580950google scholar: lookup
  18. Zerbe H, Engelke F, Klug E, Schoon HA, Leibold W. Degenerative endometrial changes do not change the functional capacity of immigrating uterine neutrophils in mares.. Reprod Domest Anim 2004 Apr;39(2):94-8.
  19. Walter I, Handler J, Miller I, Aurich C. Matrix metalloproteinase 2 (MMP-2) and tissue transglutaminase (TG 2) are expressed in periglandular fibrosis in horse mares with endometrosis.. Histol Histopathol 2005 Oct;20(4):1105-13.
    pubmed: 16136493doi: 10.14670/hh-20.1105google scholar: lookup
  20. Rodgers WH, Matrisian LM, Giudice LC, Dsupin B, Cannon P, Svitek C, Gorstein F, Osteen KG. Patterns of matrix metalloproteinase expression in cycling endometrium imply differential functions and regulation by steroid hormones.. J Clin Invest 1994 Sep;94(3):946-53.
    doi: 10.1172/jci117461pmc: PMC295134pubmed: 8083380google scholar: lookup
  21. Clutterbuck AL, Harris P, Allaway D, Mobasheri A. Matrix metalloproteinases in inflammatory pathologies of the horse.. Vet J 2010 Jan;183(1):27-38.
    doi: 10.1016/j.tvjl.2008.09.022pubmed: 19022687google scholar: lookup
  22. Zavan B, Vindigni V, Gardin C, D'Avella D, Della Puppa A, Abatangelo G, Cortivo R. Neural potential of adipose stem cells.. Discov Med 2010 Jul;10(50):37-43.
    pubmed: 20670597
  23. Zavan B, Michelotto L, Lancerotto L, Della Puppa A, D'Avella D, Abatangelo G, Vindigni V, Cortivo R. Neural potential of a stem cell population in the adipose and cutaneous tissues.. Neurol Res 2010 Feb;32(1):47-54.
    doi: 10.1179/174313209X385743pubmed: 20092695google scholar: lookup
  24. Vindigni V, Michelotto L, Lancerotto L, Puppa AD, D'Avella D, Abatangelo G, Cortivo R, Zavan B. Isolation method for a stem cell population with neural potential from skin and adipose tissue.. Neurol Res 2009 Aug 5;.
    doi: 10.1179/174313209X459200pubmed: 19660183google scholar: lookup
  25. Kenney RM, Doig PA. Equine endometrial biopsy. Current Therapy in Theriogenealogy 1986;2:726–729.
  26. Alivisatos AP, Gu W, Larabell C. Quantum dots as cellular probes.. Annu Rev Biomed Eng 2005;7:55-76.
  27. Fumuso E, Giguère S, Wade J, Rogan D, Videla-Dorna I, Bowden RA. Endometrial IL-1beta, IL-6 and TNF-alpha, mRNA expression in mares resistant or susceptible to post-breeding endometritis. Effects of estrous cycle, artificial insemination and immunomodulation.. Vet Immunol Immunopathol 2003 Nov 15;96(1-2):31-41.
    doi: 10.1016/s0165-2427(03)00137-5pubmed: 14522132google scholar: lookup
  28. Fumuso EA, Aguilar J, Giguère S, Rivulgo M, Wade J, Rogan D. Immune parameters in mares resistant and susceptible to persistent post-breeding endometritis: effects of immunomodulation.. Vet Immunol Immunopathol 2007 Jul 15;118(1-2):30-9.
    doi: 10.1016/j.vetimm.2007.04.009pubmed: 17559943google scholar: lookup
  29. Feghali CA, Wright TM. Cytokines in acute and chronic inflammation.. Front Biosci 1997 Jan 1;2:d12-26.
    pubmed: 9159205doi: 10.2741/a171google scholar: lookup
  30. Gérard N, Caillaud M, Martoriati A, Goudet G, Lalmanach AC. The interleukin-1 system and female reproduction.. J Endocrinol 2004 Feb;180(2):203-12.
    doi: 10.1677/joe.0.1800203pubmed: 14765973google scholar: lookup
  31. Kaplanski G, Marin V, Montero-Julian F, Mantovani A, Farnarier C. IL-6: a regulator of the transition from neutrophil to monocyte recruitment during inflammation.. Trends Immunol 2003 Jan;24(1):25-9.
    doi: 10.1016/s1471-4906(02)00013-3pubmed: 12495721google scholar: lookup

Citations

This article has been cited 13 times.
  1. Petrova V, Vachkova E. Outlook of Adipose-Derived Stem Cells: Challenges to Their Clinical Application in Horses. Vet Sci 2023 May 12;10(5).
    doi: 10.3390/vetsci10050348pubmed: 37235430google scholar: lookup
  2. Li W, Lin A, Qi L, Lv X, Yan S, Xue J, Mu N. Immunotherapy: A promising novel endometriosis therapy. Front Immunol 2023;14:1128301.
    doi: 10.3389/fimmu.2023.1128301pubmed: 37138868google scholar: lookup
  3. Cui M, Liu Y, Men X, Li T, Liu D, Deng Y. Large animal models in the study of gynecological diseases. Front Cell Dev Biol 2023;11:1110551.
    doi: 10.3389/fcell.2023.1110551pubmed: 36755972google scholar: lookup
  4. Alpoim-Moreira J, Fernandes C, Pimenta J, Bliebernicht M, Rebordão MR, Castelo-Branco P, Szóstek-Mioduchowska A, Skarzynski DJ, Ferreira-Dias G. Metallopeptidades 2 and 9 genes epigenetically modulate equine endometrial fibrosis. Front Vet Sci 2022;9:970003.
    doi: 10.3389/fvets.2022.970003pubmed: 36032279google scholar: lookup
  5. Uberti B, Plaza A, Henríquez C. Pre-conditioning Strategies for Mesenchymal Stromal/Stem Cells in Inflammatory Conditions of Livestock Species. Front Vet Sci 2022;9:806069.
    doi: 10.3389/fvets.2022.806069pubmed: 35372550google scholar: lookup
  6. Palumbo Piccionello A, Riccio V, Senesi L, Volta A, Pennasilico L, Botto R, Rossi G, Tambella AM, Galosi L, Marini C, Vullo C, Gigante A, Zavan B, De Francesco F, Riccio M. Adipose micro-grafts enhance tendinopathy healing in ovine model: An in vivo experimental perspective study. Stem Cells Transl Med 2021 Nov;10(11):1544-1560.
    doi: 10.1002/sctm.20-0496pubmed: 34398527google scholar: lookup
  7. Cequier A, Sanz C, Rodellar C, Barrachina L. The Usefulness of Mesenchymal Stem Cells beyond the Musculoskeletal System in Horses. Animals (Basel) 2021 Mar 25;11(4).
    doi: 10.3390/ani11040931pubmed: 33805967google scholar: lookup
  8. Bukowska J, Szóstek-Mioduchowska AZ, Kopcewicz M, Walendzik K, Machcińska S, Gawrońska-Kozak B. Adipose-Derived Stromal/Stem Cells from Large Animal Models: from Basic to Applied Science. Stem Cell Rev Rep 2021 Jun;17(3):719-738.
    doi: 10.1007/s12015-020-10049-ypubmed: 33025392google scholar: lookup
  9. Venkatarame Gowda Saralamma V, Vetrivel P, Kim SM, Ha SE, Lee HJ, Lee SJ, Kim YS, Pak JE, Lee HJ, Heo JD, Kim GS. Proteome Profiling of Membrane-Free Stem Cell Components by Nano-LS/MS Analysis and Its Anti-Inflammatory Activity. Evid Based Complement Alternat Med 2019;2019:4683272.
    doi: 10.1155/2019/4683272pubmed: 31781269google scholar: lookup
  10. Winter RL, Seeto WJ, Tian Y, Caldwell FJ, Lipke EA, Wooldridge AA. Growth and function of equine endothelial colony forming cells labeled with semiconductor quantum dots. BMC Vet Res 2018 Aug 23;14(1):247.
    doi: 10.1186/s12917-018-1572-3pubmed: 30139355google scholar: lookup
  11. Rink BE, Beyer T, French HM, Watson E, Aurich C, Donadeu FX. The Fate of Autologous Endometrial Mesenchymal Stromal Cells After Application in the Healthy Equine Uterus. Stem Cells Dev 2018 Aug 1;27(15):1046-1052.
    doi: 10.1089/scd.2018.0056pubmed: 29790424google scholar: lookup
  12. Vachkova E, Arnhold S, Petrova V, Heimann M, Koynarski T, Simeonova G, Piperkov P. Transcriptional Factors Related to Cellular Kinetics, Apoptosis, and Tumorigenicity in Equine Adipose-Derived Mesenchymal Stem Cells (ASCs) Are Influenced by the Age of the Donors. Animals (Basel) 2025 Jun 28;15(13).
    doi: 10.3390/ani15131910pubmed: 40646808google scholar: lookup
  13. Ferreira-Baptista C, Ferreira R, Fernandes MH, Gomes PS, Colaço B. Influence of the Anatomical Site on Adipose Tissue-Derived Stromal Cells' Biological Profile and Osteogenic Potential in Companion Animals. Vet Sci 2023 Nov 24;10(12).
    doi: 10.3390/vetsci10120673pubmed: 38133224google scholar: lookup