Multinucleated Tissue Research Articles

Cholesterol uptake and efflux are impaired in human trophoblast cells from pregnancies with maternal supraphysiological hypercholesterolemia

Maternal physiological (MPH) or supraphysiological hypercholesterolaemia (MSPH) occurs during pregnancy. Cholesterol trafficking from maternal to foetal circulation requires the uptake of maternal LDL and HDL by syncytiotrophoblast and cholesterol efflux from this multinucleated tissue to ApoA-I and HDL. We aimed to determine the effects of MSPH on placental cholesterol trafficking. Placental tissue and primary human trophoblast (PHT) were isolated from pregnant women with total cholesterol <280 md/dL (MPH, n = 27) or ≥280 md/dL (MSPH, n = 28). The lipid profile in umbilical cord blood from MPH and MSPH neonates was similar. The abundance of LDL receptor (LDLR) and HDL receptor (SR-BI) was comparable between MSPH and MPH placentas. However, LDLR was localized mainly in the syncytiotrophoblast surface and was associated with reduced placental levels of its ligand ApoB. In PHT from MSPH, the uptake of LDL and HDL was lower compared to MPH, without changes in LDLR and reduced levels of SR-BI. Regarding cholesterol efflux, in MSPH placentas, the abundance of cholesterol transporter ABCA1 was increased, while ABCG1 and SR-BI were reduced. In PHT from MSPH, the cholesterol efflux to ApoA-I was increased and to HDL was reduced, along with reduced levels of ABCG1, compared to MPH. Inhibition of SR-BI did not change cholesterol efflux in PHT. The TC content in PHT was comparable in MPH and MSPH cells. However, free cholesterol was increased in MSPH cells. We conclude that MSPH alters the trafficking and content of cholesterol in placental trophoblasts, which could be associated with changes in the placenta-mediated maternal-to-foetal cholesterol trafficking.

The Significance of Syncytial Tissues for the Position of the Hexactinellida in the Metazoa

Hexactinellid sponges are metazoans in which the major tissue component is a multinucleated syncytium. The preferred deepwater habitat of these sponges makes collection of hexactinellids in good condition difficult, and has hindered extensive examination of their body plan. Nonetheless, over the last three decades a number of studies have explored their ecology, histology and physiology. It has been shown that hexactinellids are extremely long-lived animals. Their cytoplasm consists of a giant, multinucleated tissue, the trabecular syncytium, which is connected via open and plugged cytoplasmic bridges to cells such as archaeocytes, choanoblasts, and cells with spherical inclusions. Because all of the sponge is cytoplasmically interconnected, electrical signals can propagate through the animal. The effector response is arrest of the feeding current. The perforate plugged junction apparently allows tissues to specialize in different ways while maintaining limited cytoplasmic continuity. Larvae of hexactinellid sponges are already largely syncytial. Although it is not known when the first syncytial tissues are formed or when perforate plugged junctions first appear during embryogenesis, evidence that embryos are cellular until gastrulation suggests that hexactinellid sponges may have evolved from cellular sponges and that syncytial tissues are not a primitive trait of the Metazoa.