The placenta acts as a protective barrier to prevent pathogens passing from mother to baby
The trophoblast (outer part of blastocyst from week 1) develops into placenta.
Trophoblast splits into syncytiotrophoblast and cytotrophoblast
Syncytiotrophoblast
direct contact with maternal blood
outer layer of multiple fused trophoblast cells
specialised systems for maternal/fetal transport
barrier to unwanted material
hormone secretion
Cytotrophoblast
inner layer of trophoblast with several specialised functions
proteolytic enzyme secretion (acts on decidua)
endometrial invasion
villous formation
angiogenesis
Uterus mainly supplied by uterine artery - branch of internal iliac artery
Uterine artery branches
A) arcuate
B) radial
C) basal
D) spiral
Arcuate artery runs circumferentially in myometrium
Spiral arteries invaded by cytotrophoblast cells and remodelled to create a low resistance/high flow pathway. These supply a maternal blood pool, the intervillous space.
Contributory mechanisms to maternal vascular development
growth factors
angiotensin II
cytokines
natural killer cells
Spiral arteries funnel, generating a wide outflow into the intervillous space.
During developing pregnancy, endothelium is replaced by endovascular cytotrophoblast cells, process facilitated by invaded natural killer and extravillous cytotrophoblast cells.
Frond-like villi grow into the intervillous space, well-perfused with fetal blood from the umbilical vessels
microvilli cover these villi, creating a huge surface area
acts as combination of lung and small intestine for the fetus
maternal and fetal blood flows are not in direct contact.
Maternal blood flow
intervillous space pressure 10 - 15 mmHg
flow 500 - 600 mL/min
uterine contractions compromise flow (e.g. in labour)
Fetal blood flow
capillary pressure 30 mmHg
flow 450 mL/min at term
The placenta is divided into 15-20 discrete sections called cotyledons
The umbilical cord carries fetal blood. It has 2 arteries carrying deoxygenated blood to the placenta, and 1 vein carrying oxygenated blood away from the placenta.
The umbilical arteries are supplied by the internal iliac arteries in the fetus.
Placenta fetal surface
covered in smooth membranes
central umbilical cord insertion
The amniotic sac has two layers: inner amnion and outer chorion.
Placenta maternal surface
exposed rough surface
adherent to uterine wall
After every delivery placental examination is required to confirm no cotyledons have been left behind.
Ultrasound shows placental localisation
Doppler shows umbilical cord insertion and can assess umbilical flow
hCG
produced from blastocyst stage
supports pregnancy in 1st trimester via corpus luteum
Progesteron produced independently by placenta
Human placental lactogen - anti-insulin action makes more glucose available for fetus
Transfer function
O2/CO2
nutrients: glucose, lipids
waste products: urea, bilirubin
hormones: cortisol
immunological: antibodies
drugs
Anti-epileptics should not be used in pregnancy as e.g. sodium valproate can cross placenta and cause cognitive difficulties and congenital abnormalities in the fetus.
Steroids and fatty acids cross the placenta by passive diffusion as they are fat soluble, small and unionised.
Glucose crosses the placenta by facilitated diffusion, mainly via GLUT1 (insulin independent)
Amino acids and minerals such as iron and calcium cross the placenta via active transport, with specific mechanisms for each
Immunoglobulins cross the placenta via endo/pinocytosis (only IgG as it is the smallest)
Water crosses the placenta by osmosis following electrolyte movement.
Placental transfer of O2/CO2 is by simple diffusion. Fetal O2 carriage is aided by polycythaemia, and higher O2 affinity of HbF. O2 transfer is further aided by the Bohr effect (shift in Hb-O2 curve by changes in local environment including pH and pCO2)
How does the Bohr effect help placental transfer?
Small right shift in maternal circulation encourages O2 unloading
Small left shift in fetal circulation encourages O2 uptake
Double Bohr effect
Placenta is generally an effective microbiological safety barrier, but is less efficient in early pregnancy (when fetal immune system is less developed)
risks include rubella, CMV, toxoplasmosis
HIV largely not transmitted during pregnancy in the Western world