Malaria in pregnancy regulates P-glycoprotein (P-gp/Abcb1a) and ABCA1 efflux transporters in the Mouse Visceral Yolk Sac

J Cell Mol Med. 2020 Sep;24(18):10636-10647. doi: 10.1111/jcmm.15682. Epub 2020 Aug 11.

Abstract

Malaria in pregnancy (MiP) induces intrauterine growth restriction (IUGR) and preterm labour (PTL). However, its effects on yolk sac morphology and function are largely unexplored. We hypothesized that MiP modifies yolk sac morphology and efflux transport potential by modulating ABC efflux transporters. C57BL/6 mice injected with Plasmodium berghei ANKA (5 × 105 infected erythrocytes) at gestational day (GD) 13.5 were subjected to yolk sac membrane harvesting at GD 18.5 for histology, qPCR and immunohistochemistry. MiP did not alter the volumetric proportion of the yolk sac's histological components. However, it increased levels of Abcb1a mRNA (encoding P-glycoprotein) and macrophage migration inhibitory factor (Mif chemokine), while decreasing Abcg1 (P < 0.05); without altering Abca1, Abcb1b, Abcg2, Snat1, Snat2, interleukin (Il)-1β and C-C Motif chemokine ligand 2 (Ccl2). Transcripts of Il-6, chemokine (C-X-C motif) ligand 1 (Cxcl1), Glut1 and Snat4 were not detectible. ABCA1, ABCG1, breast cancer resistance protein (BCRP) and P-gp were primarily immunolocalized to the cell membranes and cytoplasm of endodermic epithelium but also in the mesothelium and in the endothelium of mesodermic blood vessels. Intensity of P-gp labelling was stronger in both endodermic epithelium and mesothelium, whereas ABCA1 labelling increased in the endothelium of the mesodermic blood vessels. The presence of ABC transporters in the yolk sac wall suggests that this fetal membrane acts as an important protective gestational barrier. Changes in ABCA1 and P-gp in MiP may alter the biodistribution of toxic substances, xenobiotics, nutrients and immunological factors within the fetal compartment and participate in the pathogenesis of malaria-induced IUGR and PTL.

Keywords: Plasmodium berghei ANKA; ABCA1; ABCG1; Breast Cancer Resistance Protein (BCRP); P-glycoprotein (P-gp); malaria in pregnancy (MiP); yolk sac.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter 1 / biosynthesis*
  • ATP Binding Cassette Transporter 1 / genetics
  • ATP Binding Cassette Transporter, Subfamily B / biosynthesis*
  • ATP Binding Cassette Transporter, Subfamily B / genetics
  • Animals
  • Biological Transport
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Female
  • Fetal Growth Retardation / etiology
  • Gene Expression Regulation*
  • Inflammation
  • Malaria / complications
  • Malaria / genetics
  • Malaria / metabolism*
  • Membrane Transport Proteins / biosynthesis
  • Membrane Transport Proteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Organ Size
  • Plasmodium berghei
  • Pregnancy
  • Pregnancy Complications, Infectious / genetics
  • Pregnancy Complications, Infectious / metabolism*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Yolk Sac / metabolism*
  • Yolk Sac / ultrastructure

Substances

  • ABCA1 protein, mouse
  • ATP Binding Cassette Transporter 1
  • ATP Binding Cassette Transporter, Subfamily B
  • Cytokines
  • Membrane Transport Proteins
  • RNA, Messenger
  • multidrug resistance protein 3