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Related Concept Videos

The Y Chromosome Determines Maleness02:19

The Y Chromosome Determines Maleness

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The Y chromosome is a sex chromosome found in several vertebrates and mammals, including humans. In addition to 22 pairs of autosomes, the human males have one X chromosome and one Y chromosome. In these organisms, the presence or absence of the Y chromosome determines the development of male traits.
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size....
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Using Ex Vivo Upright Droplet Cultures of Whole Fetal Organs to Study Developmental Processes during Mouse Organogenesis
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Testosterone Exposure During Fetal Masculinization Programming Window Determines the Kidney Size in Adult Mice.

Arttu Junnila1, Kalle T Rytkönen1,2, Guillermo Martinez-Nieto1

  • 1Institute of Biomedicine, Research Centre for Integrative Physiology and Pharmacology, University of Turku, Turku, Finland.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
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PubMed
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Fetal androgen deficiency in male mice reduces adult kidney size and growth. Testosterone supplementation during development restored normal kidney size, indicating a critical programming window.

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ARHNF4AIGFBP5kidney growthmasculinization programming windowtestosterone

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Area of Science:

  • Endocrinology
  • Developmental Biology
  • Nephrology

Background:

  • Kidney size exhibits sexual dimorphism in adults, influenced by androgens.
  • The impact of developmental androgen deficiency on kidney programming is not well understood.

Purpose of the Study:

  • To investigate the hypothesis that androgens program kidney growth during fetal development.
  • To determine the effects of developmental androgen deficiency on male kidney development and adult function.

Main Methods:

  • Utilized Hsd17b3 knockout mice, which have a deficiency in testosterone production.
  • Administered testosterone supplementation during specific embryonic periods (E14.5-17.5).
  • Analyzed kidney size, nephron development, glomeruli number, and proximal tubule proliferation and size in adult mice.

Main Results:

  • Male Hsd17b3 knockout mice exhibited reduced testosterone during a critical fetal window (E15.5-18.5), leading to smaller adult kidneys.
  • Nephron development was normal, but glomeruli number and proximal tubule proliferation/size were reduced in knockout males.
  • Testosterone supplementation during fetal development normalized kidney size in adult knockout males.

Conclusions:

  • Fetal androgen deficiency programs reduced kidney growth and androgen responsiveness in adult males.
  • Androgen receptor and HNF4A signaling pathways are implicated in mediating male-specific fetal kidney growth.
  • This study identifies a novel mechanism of developmental programming affecting male kidney development.