Cargando…

Pregnancy and weaning regulate human maternal liver size and function

During pregnancy, the rodent liver undergoes hepatocyte proliferation and increases in size, followed by weaning-induced involution via hepatocyte cell death and stromal remodeling, creating a prometastatic niche. These data suggest a mechanism for increased liver metastasis in breast cancer patient...

Descripción completa

Detalles Bibliográficos
Autores principales: Q. Bartlett, Alexandra, Vesco, Kimberly K., Purnell, Jonathan Q., Francisco, Melanie, Goddard, Erica, Guan, Xiangnan, DeBarber, Andrea, Leo, Michael C., Baetscher, Eric, Rooney, William, Naugler, Willscott, Guimaraes, Alexander R., Catalano, Patrick, Xia, Zheng, Schedin, Pepper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640831/
https://www.ncbi.nlm.nih.gov/pubmed/34815335
http://dx.doi.org/10.1073/pnas.2107269118
_version_ 1784609395255017472
author Q. Bartlett, Alexandra
Vesco, Kimberly K.
Purnell, Jonathan Q.
Francisco, Melanie
Goddard, Erica
Guan, Xiangnan
DeBarber, Andrea
Leo, Michael C.
Baetscher, Eric
Rooney, William
Naugler, Willscott
Guimaraes, Alexander R.
Catalano, Patrick
Xia, Zheng
Schedin, Pepper
author_facet Q. Bartlett, Alexandra
Vesco, Kimberly K.
Purnell, Jonathan Q.
Francisco, Melanie
Goddard, Erica
Guan, Xiangnan
DeBarber, Andrea
Leo, Michael C.
Baetscher, Eric
Rooney, William
Naugler, Willscott
Guimaraes, Alexander R.
Catalano, Patrick
Xia, Zheng
Schedin, Pepper
author_sort Q. Bartlett, Alexandra
collection PubMed
description During pregnancy, the rodent liver undergoes hepatocyte proliferation and increases in size, followed by weaning-induced involution via hepatocyte cell death and stromal remodeling, creating a prometastatic niche. These data suggest a mechanism for increased liver metastasis in breast cancer patients with recent childbirth. It is unknown whether the human liver changes in size and function during pregnancy and weaning. In this study, abdominal imaging was obtained in healthy women at early and late pregnancy and postwean. During pregnancy time points, glucose production and utilization and circulating bile acids were measured. Independently of weight gain, most women’s livers increased in size with pregnancy, then returned to baseline postwean. Putative roles for bile acids in liver growth and regression were observed. Together, the data support the hypothesis that the human liver is regulated by reproductive state with growth during pregnancy and volume loss postwean. These findings have implications for sex-specific liver diseases and for breast cancer outcomes.
format Online
Article
Text
id pubmed-8640831
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-86408312021-12-13 Pregnancy and weaning regulate human maternal liver size and function Q. Bartlett, Alexandra Vesco, Kimberly K. Purnell, Jonathan Q. Francisco, Melanie Goddard, Erica Guan, Xiangnan DeBarber, Andrea Leo, Michael C. Baetscher, Eric Rooney, William Naugler, Willscott Guimaraes, Alexander R. Catalano, Patrick Xia, Zheng Schedin, Pepper Proc Natl Acad Sci U S A Biological Sciences During pregnancy, the rodent liver undergoes hepatocyte proliferation and increases in size, followed by weaning-induced involution via hepatocyte cell death and stromal remodeling, creating a prometastatic niche. These data suggest a mechanism for increased liver metastasis in breast cancer patients with recent childbirth. It is unknown whether the human liver changes in size and function during pregnancy and weaning. In this study, abdominal imaging was obtained in healthy women at early and late pregnancy and postwean. During pregnancy time points, glucose production and utilization and circulating bile acids were measured. Independently of weight gain, most women’s livers increased in size with pregnancy, then returned to baseline postwean. Putative roles for bile acids in liver growth and regression were observed. Together, the data support the hypothesis that the human liver is regulated by reproductive state with growth during pregnancy and volume loss postwean. These findings have implications for sex-specific liver diseases and for breast cancer outcomes. National Academy of Sciences 2021-11-22 2021-11-30 /pmc/articles/PMC8640831/ /pubmed/34815335 http://dx.doi.org/10.1073/pnas.2107269118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Q. Bartlett, Alexandra
Vesco, Kimberly K.
Purnell, Jonathan Q.
Francisco, Melanie
Goddard, Erica
Guan, Xiangnan
DeBarber, Andrea
Leo, Michael C.
Baetscher, Eric
Rooney, William
Naugler, Willscott
Guimaraes, Alexander R.
Catalano, Patrick
Xia, Zheng
Schedin, Pepper
Pregnancy and weaning regulate human maternal liver size and function
title Pregnancy and weaning regulate human maternal liver size and function
title_full Pregnancy and weaning regulate human maternal liver size and function
title_fullStr Pregnancy and weaning regulate human maternal liver size and function
title_full_unstemmed Pregnancy and weaning regulate human maternal liver size and function
title_short Pregnancy and weaning regulate human maternal liver size and function
title_sort pregnancy and weaning regulate human maternal liver size and function
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640831/
https://www.ncbi.nlm.nih.gov/pubmed/34815335
http://dx.doi.org/10.1073/pnas.2107269118
work_keys_str_mv AT qbartlettalexandra pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT vescokimberlyk pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT purnelljonathanq pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT franciscomelanie pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT goddarderica pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT guanxiangnan pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT debarberandrea pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT leomichaelc pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT baetschereric pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT rooneywilliam pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT nauglerwillscott pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT guimaraesalexanderr pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT catalanopatrick pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT xiazheng pregnancyandweaningregulatehumanmaternalliversizeandfunction
AT schedinpepper pregnancyandweaningregulatehumanmaternalliversizeandfunction