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Animal reproduction science2015; 163; 179-186; doi: 10.1016/j.anireprosci.2015.11.010

Acrosin-binding protein (ACRBP) in the testes of stallions.

Abstract: Acrosin Binding Protein (ACRBP) is specifically localized in the acrosome of germ cells of several species, including mice, pigs, guinea pigs, and humans. The main objective of this study was to investigate ACRBP patterns in the germ cells of stallions at different reproductive stages and seminiferous tubule stages using Western blot, immunohistochemistry, and immunocytochemistry techniques. The stallion reproductive stages were classified as follows: pre-pubertal and post-pubertal stages based on the presence/absence of lumen opening in the seminiferous tubules and full spermatogenesis. The protein band associated with the presence of ACRBP appeared at approximately 35-kDa position, indicating that the antibody used in this study recognizes the mature form of ACRBP. During the pre-pubertal stages, immunolabeling did not detect the presence of ACRBP in the germ cells. However, during the post-pubertal stage, immunolabeling of the ACRBP was observed in the pachytene spermatocyte as well as for round, elongating, and elongated spermatids, and in some spermatozoa. In conclusion, the ACRBP can be used as a molecular marker for pachytene spermatocytes, and for round, elongating, and elongated spermatids. The ACRBP can be used to monitor either normal spermatogenesis in the testicular tissues, or germ cell development in vitro. Because the ACRBP is present in the germ cells of stallions that have undergone puberty, it can be used as an indicator for the sexual maturation of stallions.
Publication Date: 2015-11-10 PubMed ID: 26597026DOI: 10.1016/j.anireprosci.2015.11.010Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research examines the presence and distribution pattern of Acrosin Binding Protein (ACRBP) in the testes of stallions across different reproductive stages. The study findings indicate that ACRBP, found within germ cells in stallions after puberty, could be used as a molecular marker indicating normal sperm development or sexual maturation.

Objective

  • The primary objective of this study was to investigate the distribution and patterns of Acrosin Binding Protein (ACRBP) in germ cells of stallions across different reproductive and seminiferous tubule stages.

Methodology

  • The researchers employed techniques such as Western blot, immunohistochemistry, and immunocytochemistry to carry out the investigation.
  • They categorized the reproductive stages of the stallions into pre-pubertal and post-pubertal stages. This categorization was based on the existence or non-existence of lumen opening in the seminiferous tubules and full spermatogenesis.

Findings

  • The results showed that the protein band, associated with the presence of ACRBP, appeared near the 35-kDa position. This signified that the antibody utilized in the research recognizes the mature form of ACRBP.
  • During the pre-pubertal stage, the ACRBP was not detectable in the germ cells according to the research’s immunolabeling technique.
  • In contrast, during the post-pubertal stage, immunolabeling was able to depict ACRBP presence in the pachytene spermatocyte, and also in round, elongating, and elongated spermatids, and in some spermatozoa.

Implication

  • The study concludes that ACRBP can serve as a molecular marker for pachytene spermatocytes and for round, elongating, and elongated spermatids.
  • This protein can be used to monitor standard spermatogenesis in testicular tissues or germ cell development in vitro.
  • The presence of ACRBP in germ cells of stallions post puberty positions it as an indicator for the determining sexual maturation of stallions.

Cite This Article

APA
Kim JT, Jung HJ, Song H, Yoon MJ. (2015). Acrosin-binding protein (ACRBP) in the testes of stallions. Anim Reprod Sci, 163, 179-186. https://doi.org/10.1016/j.anireprosci.2015.11.010

Publication

ISSN: 1873-2232
NlmUniqueID: 7807205
Country: Netherlands
Language: English
Volume: 163
Pages: 179-186
PII: S0378-4320(15)30053-1

Researcher Affiliations

Kim, J T
  • Department of Animal Science and Biotechnology, Kyungpook National University, Sangju 742-711, Republic of Korea.
Jung, H J
  • Department of Animal Science and Biotechnology, Kyungpook National University, Sangju 742-711, Republic of Korea.
Song, H
  • Department of Animal Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea.
Yoon, M J
  • Department of Animal Science and Biotechnology, Kyungpook National University, Sangju 742-711, Republic of Korea; Department of Horse, Companion and Wild Animal Science, Kyungpook National University, Sangju 742-711, Republic of Korea. Electronic address: mjyoon@knu.ac.kr.

MeSH Terms

  • Acrosin / metabolism
  • Animals
  • Biomarkers
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Gene Expression Regulation / physiology
  • Horses / physiology
  • Male
  • Protein Transport
  • RNA-Binding Proteins / physiology
  • Testis / metabolism

Citations

This article has been cited 4 times.
  1. Fu J, Yingying Ge, Qingmei Zhang, Lin Y, Liu C, Nong W, Luo X, Xiao S, Xie X, Luo B. Immunohistochemistry Study of OY-TES-1 Location in Fetal and Adult Human Tissues.. J Healthc Eng 2022;2022:7052830.
    doi: 10.1155/2022/7052830pubmed: 35463688google scholar: lookup
  2. Cruz A, Sullivan DB, Doty KF, Hess RA, Canisso IF, Reddi PP. Acrosomal marker SP-10 (gene name Acrv1) for staging of the cycle of seminiferous epithelium in the stallion.. Theriogenology 2020 Oct 15;156:214-221.
  3. Pinto TMF, Moreira RF, Matos MNC, Soares VVM, Aguiar MVA, de Aragão PTTD, Alves JG, Moreno FBMB, Monteiro-Moreira ACO, Costa CRR, de Lima JL, Eloy AMX, da Cunha RMS. Evaluation of the proteomic profiles of ejaculated spermatozoa from Saanen bucks ( Capra hircus ).. Anim Reprod 2019 Nov 18;16(4):902-913.
  4. Chen G, Chen J, Liu H, Chen S, Zhang Y, Li P, Thierry-Mieg D, Thierry-Mieg J, Mattes W, Ning B, Shi T. Comprehensive Identification and Characterization of Human Secretome Based on Integrative Proteomic and Transcriptomic Data.. Front Cell Dev Biol 2019;7:299.
    doi: 10.3389/fcell.2019.00299pubmed: 31824949google scholar: lookup