Expression and cellular localization of inhibin alpha-subunit mRNA in equine fetal gonads.
Abstract: The expression of inhibin alpha-subunit mRNA in equine fetal gonads during pregnancy (Days 90 to 300) was examined by means of Northern blot analysis. In all samples examined, a single species of transcript was detected at the size of 1.5 kb. A digoxigenin-labeled antisense cRNA probe specific to equine inhibin alpha-subunit was synthesized and in situ hybridization analysis to locate the inhibin alpha-subunit mRNA positive cells was performed using frozen tissue sections of equine fetal ovary (day 150 of pregnancy) and equine fetal testis (day 180 of pregnancy). In the fetal ovary, positive cells were seen throughout the interstitial area but did not show any particular localization. In the fetal testis, on the other hand, the antisense cRNA hybridized almost exclusively to the interstitial cells surrounding developing seminiferous cords and Sertoli cells within the cords. Positive signals were also detected in a limited number of the interstitial cells located away from the cords. These results suggest that in equine fetal gonads, inhibin and/or inhibin alpha-subunit related molecules such as the monomeric form are produced and these molecules may have a paracrine/autocrine role within the gonads.
Publication Date: 1997-07-01 PubMed ID: 9271452DOI: 10.1292/jvms.59.569Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article explores the expression of inhibin alpha-subunit mRNA in the fetal gonads of horses during pregnancy, and how this may have an important role within these reproductive organs.
Experimental Process
- The expression of inhibin alpha-subunit mRNA in equine fetal gonads was examined during pregnancy, between Days 90 to 300. The method of examination used was Northern blot analysis. Northern blot analysis is a technique that allows for the study of RNA molecules, providing insights into the gene’s mRNA products – including their sizes and abundance.
- The existence of the mRNA was confirmed by the detection of a single species of transcript of the size of 1.5 kb. This highlights the presence of the inhibin alpha-subunit mRNA within the fetal gonads.
- A digoxigenin-labeled antisense cRNA probe specific to the equine inhibin alpha-subunit was synthesized for the study. This probe was used to conduct in situ hybridization analysis which allowed the research team to pinpoint where the inhibin alpha-subunit mRNA positive cells were located in the gonads.
Results
- The research included an examination of both fetal ovaries on the 150th day of pregnancy and fetal testes on the 180th day of pregnancy. In the fetal ovary, positive cells were found throughout the interstitial area but had no specific localization.
- On the contrary, in the fetal testis, the antisense cRNA probe hybridized almost exclusively to the interstitial cells surrounding the developing seminiferous cords and Sertoli cells that resided within the cords. Additionally, positive signals were also detected in a limited number of interstitial cells located away from the cords.
Conclusions
- The findings from the study suggest that the equine fetal gonads produce inhibin and/or inhibin alpha-subunit related molecules such as the monomeric form.
- The researchers believe these molecules may perform a paracrine or autocrine role within the gonads. Paracrine signaling is a form of cell communication where the cell produces signals to induce changes in nearby cells. Autocrine signaling is a form of cell communication in which a cell secretes a hormone or chemical messenger that binds to autocrine receptors on the same cell, leading to changes in the cell.
Cite This Article
APA
Yamanouchi K, Hirasawa K, Hondo E, Hasegawa T, Ikeda A, Sugawara Y, Matsuyama S, Miyazawa K, Sawasaki T, Tojo H, Tachi C, Takahashi M.
(1997).
Expression and cellular localization of inhibin alpha-subunit mRNA in equine fetal gonads.
J Vet Med Sci, 59(7), 569-573.
https://doi.org/10.1292/jvms.59.569 Publication
Researcher Affiliations
- Institute of Animal Resource Sciences, Graduate School of Agricultural and Life Science, The University of Tokyo, Japan.
MeSH Terms
- Animals
- Female
- Fetus
- Gestational Age
- Glycoprotein Hormones, alpha Subunit / biosynthesis
- Horses
- In Situ Hybridization
- Inhibins / biosynthesis
- Male
- Ovary / embryology
- Ovary / metabolism
- Pregnancy
- RNA, Antisense
- RNA, Messenger / analysis
- RNA, Messenger / biosynthesis
- Sertoli Cells / metabolism
- Testis / embryology
- Testis / metabolism
- Transcription, Genetic
Citations
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