Your browser doesn't support javascript.
loading
Generation and characterization of human Fetal membrane and Decidual cell lines for reproductive biology experiments†.
Radnaa, Enkhtuya; Urrabaz-Garza, Rheanna; Elrod, Nathan D; de Castro Silva, Mariana; Pyles, Richard; Han, Arum; Menon, Ramkumar.
Afiliación
  • Radnaa E; Division of Maternal-Fetal Medicine and Perinatal Research, Department of Obstetrics and Gynaecology, The University of Texas Medical Branch at Galveston, Galveston, Texas, USA.
  • Urrabaz-Garza R; Division of Maternal-Fetal Medicine and Perinatal Research, Department of Obstetrics and Gynaecology, The University of Texas Medical Branch at Galveston, Galveston, Texas, USA.
  • Elrod ND; Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555-0144, USA.
  • de Castro Silva M; Division of Maternal-Fetal Medicine and Perinatal Research, Department of Obstetrics and Gynaecology, The University of Texas Medical Branch at Galveston, Galveston, Texas, USA.
  • Pyles R; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555-0144, USA.
  • Han A; Department of Electrical and Computer Engineering, Department of Biomedical Engineering, Texas A&M University, College Station, Texas 77843-3128, USA.
  • Menon R; Division of Maternal-Fetal Medicine and Perinatal Research, Department of Obstetrics and Gynaecology, The University of Texas Medical Branch at Galveston, Galveston, Texas, USA.
Biol Reprod ; 106(3): 568-582, 2022 03 19.
Article en En | MEDLINE | ID: mdl-34935931
Human fetal membrane and maternal decidua parietalis form one of the major feto-maternal interfaces during pregnancy. Studies on this feto-maternal interface is limited as several investigators have limited access to the placenta, and experience difficulties to isolate and maintain primary cells. Many cell lines that are currently available do not have the characteristics or properties of their primary cells of origin. Therefore, we created, characterized the immortalized cells from primary isolates from fetal membrane-derived amnion epithelial cells, amnion and chorion mesenchymal cells, chorion trophoblast cells and maternal decidua parietalis cells. Primary cells were isolated from a healthy full-term, not in labor placenta. Primary cells were immortalized using either a HPV16E6E7 retroviral or a SV40T lentiviral system. The immortalized cells were characterized for the morphology, cell type-specific markers, and cell signalling pathway activation. Genomic stability of these cells was tested using RNA seq, karyotyping, and short tandem repeats DNA analysis. Immortalized cells show their characteristic morphology, and express respective epithelial, mesenchymal and decidual markers similar to that of primary cells. Gene expression of immortalized and primary cells were highly correlated (R = 0.798 to R = 0.974). Short tandem repeats DNA analysis showed in the late passage number (>P30) of cell lines matched 84-100% to the early passage number (
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Decidua / Membranas Extraembrionarias Límite: Female / Humans / Pregnancy Idioma: En Revista: Biol Reprod Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Decidua / Membranas Extraembrionarias Límite: Female / Humans / Pregnancy Idioma: En Revista: Biol Reprod Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos