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Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants

BACKGROUND: During normal human kidney development, nephrogenesis (the formation of nephrons) is complete by term birth, with the majority of nephrons formed late in gestation. The aim of this study was to morphologically examine nephrogenesis in fetal human kidneys from 20 to 41 weeks of gestation....

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Autores principales: Ryan, Danica, Sutherland, Megan R., Flores, Tracey J., Kent, Alison L., Dahlstrom, Jane E., Puelles, Victor G., Bertram, John F., McMahon, Andrew P., Little, Melissa H., Moore, Lynette, Black, Mary Jane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828465/
https://www.ncbi.nlm.nih.gov/pubmed/29329932
http://dx.doi.org/10.1016/j.ebiom.2017.12.016
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author Ryan, Danica
Sutherland, Megan R.
Flores, Tracey J.
Kent, Alison L.
Dahlstrom, Jane E.
Puelles, Victor G.
Bertram, John F.
McMahon, Andrew P.
Little, Melissa H.
Moore, Lynette
Black, Mary Jane
author_facet Ryan, Danica
Sutherland, Megan R.
Flores, Tracey J.
Kent, Alison L.
Dahlstrom, Jane E.
Puelles, Victor G.
Bertram, John F.
McMahon, Andrew P.
Little, Melissa H.
Moore, Lynette
Black, Mary Jane
author_sort Ryan, Danica
collection PubMed
description BACKGROUND: During normal human kidney development, nephrogenesis (the formation of nephrons) is complete by term birth, with the majority of nephrons formed late in gestation. The aim of this study was to morphologically examine nephrogenesis in fetal human kidneys from 20 to 41 weeks of gestation. METHODS: Kidney samples were obtained at autopsy from 71 infants that died acutely in utero or within 24 h after birth. Using image analysis, nephrogenic zone width, the number of glomerular generations, renal corpuscle cross-sectional area and the cellular composition of glomeruli were examined. Kidneys from female and male infants were analysed separately. FINDINGS: The number of glomerular generations formed within the fetal kidneys was directly proportional to gestational age, body weight and kidney weight, with variability between individuals in the ultimate number of generations (8 to 12) and in the timing of the cessation of nephrogenesis (still ongoing at 37 weeks gestation in one infant). There was a slight but significant (r(2) = 0.30, P = 0.001) increase in renal corpuscle cross-sectional area from mid gestation to term in females, but this was not evident in males. The proportions of podocytes, endothelial and non-epithelial cells within mature glomeruli were stable throughout gestation. INTERPRETATION: These findings highlight spatial and temporal variability in nephrogenesis in the developing human kidney, whereas the relative cellular composition of glomeruli does not appear to be influenced by gestational age.
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spelling pubmed-58284652018-02-28 Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants Ryan, Danica Sutherland, Megan R. Flores, Tracey J. Kent, Alison L. Dahlstrom, Jane E. Puelles, Victor G. Bertram, John F. McMahon, Andrew P. Little, Melissa H. Moore, Lynette Black, Mary Jane EBioMedicine Research Paper BACKGROUND: During normal human kidney development, nephrogenesis (the formation of nephrons) is complete by term birth, with the majority of nephrons formed late in gestation. The aim of this study was to morphologically examine nephrogenesis in fetal human kidneys from 20 to 41 weeks of gestation. METHODS: Kidney samples were obtained at autopsy from 71 infants that died acutely in utero or within 24 h after birth. Using image analysis, nephrogenic zone width, the number of glomerular generations, renal corpuscle cross-sectional area and the cellular composition of glomeruli were examined. Kidneys from female and male infants were analysed separately. FINDINGS: The number of glomerular generations formed within the fetal kidneys was directly proportional to gestational age, body weight and kidney weight, with variability between individuals in the ultimate number of generations (8 to 12) and in the timing of the cessation of nephrogenesis (still ongoing at 37 weeks gestation in one infant). There was a slight but significant (r(2) = 0.30, P = 0.001) increase in renal corpuscle cross-sectional area from mid gestation to term in females, but this was not evident in males. The proportions of podocytes, endothelial and non-epithelial cells within mature glomeruli were stable throughout gestation. INTERPRETATION: These findings highlight spatial and temporal variability in nephrogenesis in the developing human kidney, whereas the relative cellular composition of glomeruli does not appear to be influenced by gestational age. Elsevier 2017-12-20 /pmc/articles/PMC5828465/ /pubmed/29329932 http://dx.doi.org/10.1016/j.ebiom.2017.12.016 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Ryan, Danica
Sutherland, Megan R.
Flores, Tracey J.
Kent, Alison L.
Dahlstrom, Jane E.
Puelles, Victor G.
Bertram, John F.
McMahon, Andrew P.
Little, Melissa H.
Moore, Lynette
Black, Mary Jane
Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants
title Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants
title_full Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants
title_fullStr Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants
title_full_unstemmed Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants
title_short Development of the Human Fetal Kidney from Mid to Late Gestation in Male and Female Infants
title_sort development of the human fetal kidney from mid to late gestation in male and female infants
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828465/
https://www.ncbi.nlm.nih.gov/pubmed/29329932
http://dx.doi.org/10.1016/j.ebiom.2017.12.016
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