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Reproduction in domestic animals = Zuchthygiene2008; 45(2); 315-322; doi: 10.1111/j.1439-0531.2008.01307.x

Comparative immunolocalization of GLUTs 1, 2, 3 and 5 in boar, stallion and dog spermatozoa.

Abstract: Spermatozoa, as other eukaryotic cells, need hexoses to produce energy to maintain membrane homeostasis, to move along the female genital tract and to carry the male genome to the female gamete. GLUTs are a family of proteins that permit and improve the passive transport of hexoses inside cells. This study was aimed at investigating the presence and localization of GLUTs 1, 2, 3 and 5 in boar, stallion and dog spermatozoa by both immunofluorescence and western blotting. GLUTs exhibited a peculiar distribution along the sperm cell depending on the isoforms considered, the hexose they transport and the different species. The localization of GLUTs after capacitation and acrosome reaction highlighted the possible changes in their distribution because of the different functional moment. Only in dog spermatozoa changes in GLUTs distribution were demonstrated; these changes could be related to the different metabolic needs and modifications occurring in the sperm cell.
Publication Date: 2008-12-02 PubMed ID: 19055550DOI: 10.1111/j.1439-0531.2008.01307.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article investigates the presence and location of glucose transporters (GLUTs) in the sperm cells of boars, stallions, and dogs. The study explores how the distribution of these GLUTs can change and how this correlates to the different functional needs of the sperm cells.

Research Focus and Methodology

  • The research focuses on understanding the role of GLUTs, which are proteins that help transport glucose into cells, in the sperm cells of boars, stallions, and dogs. Sperm cells require glucose to produce energy for maintaining membrane stability and movement along the reproductive tract.
  • To identify the presence and location of the GLUTs, two methods were used – immunofluorescence (a method that uses fluorescent dyes to identify proteins etc. in cells) and western blotting (a technique used to separate and identify proteins).
  • The investigation examines four different GLUT prototypes, numbered 1, 2, 3, and 5.

Findings and Implications

  • The research found that the GLUTs exhibited variable distribution along the sperm cell, depending on the GLUT prototype considered, the kind of glucose they transported, and the species in question.
  • Part of the study involved exploring the location of GLUTs after capacitation (maturation process that makes sperm capable of fertilizing an egg) and acrosome reaction (process releasing enzymes needed for the sperm to penetrate the egg).
  • The results showed potential changes in GLUT distribution due to these different processes. However, interestingly, it was only in dog spermatozoa that changes in GLUT distribution were definitively demonstrated.
  • The change in GLUT distribution in dog sperm cells might be related to the different metabolic needs and modifications that occur in the cell. However, the study does not elaborate on exactly what these changes were and their specific implications for sperm function.
  • This study adds on to the understanding of sperm cell energy and glucose metabolism, with possibility for more targeted advancements in animal reproduction techniques and treatments.

Cite This Article

APA
Bucci D, Isani G, Spinaci M, Tamanini C, Mari G, Zambelli D, Galeati G. (2008). Comparative immunolocalization of GLUTs 1, 2, 3 and 5 in boar, stallion and dog spermatozoa. Reprod Domest Anim, 45(2), 315-322. https://doi.org/10.1111/j.1439-0531.2008.01307.x

Publication

ISSN: 1439-0531
NlmUniqueID: 9015668
Country: Germany
Language: English
Volume: 45
Issue: 2
Pages: 315-322

Researcher Affiliations

Bucci, D
  • Dipartimento di Morfofisiologia Veterinaria e Produzioni Animali (DIMORFIPA), Università di Bologna, Ozzano Emilia, Bologna, Italia. diego.bucci3@unibo.it
Isani, G
    Spinaci, M
      Tamanini, C
        Mari, G
          Zambelli, D
            Galeati, G

              MeSH Terms

              • Acrosome Reaction
              • Animals
              • Blotting, Western
              • Dogs / physiology
              • Fluorescent Antibody Technique / veterinary
              • Glucose Transport Proteins, Facilitative / genetics
              • Glucose Transport Proteins, Facilitative / metabolism
              • Horses / physiology
              • Male
              • Protein Transport / physiology
              • Spermatozoa / metabolism
              • Swine / physiology

              Citations

              This article has been cited 10 times.
              1. Bucci D, Spinaci M, Bustamante-Filho IC, Nesci S. The sperm mitochondria: clues and challenges.. Anim Reprod 2022;19(4):e20220131.
                doi: 10.1590/1984-3143-AR2022-0131pubmed: 36819482google scholar: lookup
              2. Schäfer-Somi S, Colombo M, Luvoni GC. Canine Spermatozoa-Predictability of Cryotolerance.. Animals (Basel) 2022 Mar 15;12(6).
                doi: 10.3390/ani12060733pubmed: 35327130google scholar: lookup
              3. Bucci D, Spinaci M, Galeati G, Tamanini C. Different approaches for assessing sperm function.. Anim Reprod 2020 May 22;16(1):72-80.
                doi: 10.21451/1984-3143-AR2018-122pubmed: 33299480google scholar: lookup
              4. Delgado-Bermúdez A, Llavanera M, Recuero S, Mateo-Otero Y, Bonet S, Barranco I, Fernandez-Fuertes B, Yeste M. Effect of AQP Inhibition on Boar Sperm Cryotolerance Depends on the Intrinsic Freezability of the Ejaculate.. Int J Mol Sci 2019 Dec 11;20(24).
                doi: 10.3390/ijms20246255pubmed: 31835821google scholar: lookup
              5. Delgado-Bermúdez A, Llavanera M, Fernández-Bastit L, Recuero S, Mateo-Otero Y, Bonet S, Barranco I, Fernández-Fuertes B, Yeste M. Aquaglyceroporins but not orthodox aquaporins are involved in the cryotolerance of pig spermatozoa.. J Anim Sci Biotechnol 2019;10:77.
                doi: 10.1186/s40104-019-0388-8pubmed: 31636902google scholar: lookup
              6. Vitavska O, Wieczorek H. Putative role of an SLC45 H(+)/sugar cotransporter in mammalian spermatozoa.. Pflugers Arch 2017 Nov;469(11):1433-1442.
                doi: 10.1007/s00424-017-2024-9pubmed: 28689241google scholar: lookup
              7. Gibb Z, Aitken RJ. The Impact of Sperm Metabolism during In Vitro Storage: The Stallion as a Model.. Biomed Res Int 2016;2016:9380609.
                doi: 10.1155/2016/9380609pubmed: 26881234google scholar: lookup
              8. Lacombe VA. Expression and regulation of facilitative glucose transporters in equine insulin-sensitive tissue: from physiology to pathology.. ISRN Vet Sci 2014;2014:409547.
                doi: 10.1155/2014/409547pubmed: 24977043google scholar: lookup
              9. Cura AJ, Carruthers A. Role of monosaccharide transport proteins in carbohydrate assimilation, distribution, metabolism, and homeostasis.. Compr Physiol 2012 Apr;2(2):863-914.
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              10. Terrell KA, Wildt DE, Anthony NM, Bavister BD, Leibo SP, Penfold LM, Marker LL, Crosier AE. Evidence for compromised metabolic function and limited glucose uptake in spermatozoa from the teratospermic domestic cat (Felis catus) and cheetah (Acinonyx jubatus).. Biol Reprod 2010 Nov;83(5):833-41.
                doi: 10.1095/biolreprod.110.085639pubmed: 20650882google scholar: lookup