TMED2/emp24 is required in both the chorion and the allantois for placental labyrinth layer development

Developmental biology

Loydie A. Jerome-Majewska^1,2,3,4¹  Wenyang Hou^1² 

[1] Department of Anatomy and Cell Biology, McGill University, Montreal, QC, Canada^2;Department of Human Genetics, McGill University, 1205 Avenue Docteur Penfield, N5/13, Montreal, QC, Canada^1;Department of Pediatrics, McGill University, 1001 Decarie Blvd, EM02210, Montreal, QC, Canada H4A 3J1^3;McGill University Health Centre Glen Site, 1001 Decarie Blvd, EM0.2210, Montreal, QC, Canada H4A 3J1^4

关键词: Chorion;    Allantois;    Chorioallantoic attachment;    Ex vivo explant;    Placenta;    Labyrinth development;    Tmed2;    P24;    Emp24;   

DOI  :  10.1016/j.ydbio.2018.09.012

学科分类：生物科学（综合）

来源: Academic Press

【 摘 要 】

TMED2, a member of the transmembrane emp24 domain (TMED) family, is required for transport of cargo proteins between the ER and Golgi. TMED2 is also important for normal morphogenesis of mouse embryos and their associated placenta, and in fact Tmed2 homozygous mutant embryos arrest at mid-gestation due to a failure of placental labyrinth layer formation. Differentiation of the placental labyrinth layer depends on chorioallantoic attachment (contact between the chorion and allantois), and branching morphogenesis (mingling of cells from these two tissues). Since Tmed2 mRNA was found in both the chorion and allantois, and 50% of Tmed2 homozygous mutant embryos failed to undergo chorioallantoic attachment, the tissue-specific requirement of Tmed2 during placental labyrinth layer formation remained a mystery. Herein, we report differential localization of TMED2 protein in the chorion and allantois, abnormal ER retention of Fibronectin in Tmed2 homozygous mutant allantoises and cell-autonomous requirement for Tmed2 in the chorion for chorioallantoic attachment and fusion. Using an ex vivo model of explanted chorions and allantoises, we showed that chorioallantoic attachment failed to occur in 50% of samples when homozygous mutant chorions were recombined with wild type allantoises. Furthermore, though expression of genes associated with trophoblast differentiation was maintained in Tmed2 mutant chorions with chorioallantoic attachment, expression of these genes was attenuated. In addition, Tmed2 homozygous mutant allantoises could undergo branching morphogenesis, however the region of mixing between mutant and wild type cells was reduced, and expression of genes associated with trophoblast differentiation was also attenuated. Our data also suggest that Fibronectin is a cargo protein of TMED2 and indicates that Tmed2 is required cell-autonomously and non-autonomously in the chorion and the allantois for placental labyrinth layer formation.

【 授权许可】

CC BY