Allometric scaling relationships in mouse placenta

Author:

Saghian Rojan12ORCID,Cahill Lindsay S.13,Debebe Sarah K.124,Rahman Anum124,Serghides Lena567,McDonald Chloe R.89,Weckman Andrea M.910,Kain Kevin C.8911,Sled John G.12412

Affiliation:

1. Mouse Imaging Centre, 25 Orde Street, Toronto, Ontario, Canada

2. Translational Medicine, Hospital for Sick Children, Toronto, Ontario, Canada

3. Department of Chemistry, Memorial University of Newfoundland, Newfoundland and Labrador, St John’s, Canada

4. Department of Medical Biophysics, University Health Network-Toronto General Hospital, Toronto, Ontario, Canada

5. Department of Immunology and Institute of Medical Sciences, University Health Network-Toronto General Hospital, Toronto, Ontario, Canada

6. Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada

7. Women’s College Research Institute, Women’s College Hospital, Toronto, Ontario, Canada

8. Institute of Medical Science, University Health Network-Toronto General Hospital, Toronto, Ontario, Canada

9. Sandra A. Rotman Laboratories, Sandra Rotman Centre for Global Health, University Health Network-Toronto General Hospital, Toronto, Ontario, Canada

10. Department of Laboratory Medicine and Pathobiology, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada

11. Tropical Disease Unit, Division of Infectious Diseases, Department of Medicine, University of Toronto, Toronto, Ontario, Canada

12. Department of Obstetrics and Gynecology, University of Toronto, Toronto, Ontario, Canada

Abstract

Fetal growth and maturation are highly intertwined with placental development during pregnancy. Here we used placental vascular morphology measurements (depth and span) as well as the umbilical artery (UA) diameter of previously published studies on three different mouse strains (C57BL6/J, CD-1 and BALB/c), which were exposed to different conditions (combination antiretroviral therapy, chronic maternal hypoxia and malaria infection) at different embryonic days, to test the hypothesis that placental vascularization and specifically the UA size affect conceptus weight. Interaction of each study parameter with embryonic day, strain and exposure to treatments are studied to investigate the stability of the scaling relationships across and/or within strains and conditions. In addition, the effect of UA diameter on the placental growth measurements (depth and span) is studied. These results show that the power-law scaling relationship of conceptus weight and placental depth with the UA diameter is conserved across strains and conditions with the scaling exponent of approximately 3/8 and 5/8, respectively. By contrast, the relationship between conceptus weight and either the placental span or depth is different between strains and conditions, suggesting multiple mechanisms of vascular adaptation.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development of Health Grant

Canadian Institutes of Health Research (CIHR) Foundation grant

Canadian Institutes of Health Research Grant

Canadian Foundation for AIDS Research

Canada Research Chair Program

CIHR Studentships

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

Reference43 articles.

1. The Role of the Placenta in Fetal Programming—A Review

2. The significance of placental/fetal weight ratios

3. Relationship of fetal and placental weight in human beings: fetal/placental weight ratios at various gestational ages and birth weight distributions;Molteni R;J. Reprod. Med.,1978

4. Feto-placental weight ratio;Stieve H;Anay Anz,1940

5. THE WEIGHT OF THE PLACENTA IN RELATION TO BIRTHWEIGHT

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