TY - JOUR
T1 - Organ-on-chip of the cervical epithelial layer
T2 - A platform to study normal and pathological cellular remodeling of the cervix
AU - Tantengco, Ourlad Alzeus G.
AU - Richardson, Lauren S.
AU - Medina, Paul Mark B.
AU - Han, Arum
AU - Menon, Ramkumar
N1 - Publisher Copyright:
© 2021 Federation of American Societies for Experimental Biology
PY - 2021/4
Y1 - 2021/4
N2 - Damage to the cervical epithelial layer due to infection and inflammation is associated with preterm birth. However, the individual and/or collective roles of cervical epithelial layers in maintaining cervical integrity remain unclear during infection/inflammation. To determine the intercellular interactions, we developed an organ-on-chip of the cervical epithelial layer (CE-OOC) composed of two co-culture chambers connected by microchannels, recapitulating the ectocervical and endocervical epithelial layers. Further, we tested the interactions between cells from each distinct region and their contributions in maintaining cervical integrity in response to LPS and TNFα stimulations. The co-culture of ectocervical and endocervical cells facilitated cellular migration of both epithelial cells inside the microchannels. Compared to untreated controls, both LPS and TNFα increased apoptosis, necrosis, and senescence as well as increased pro-inflammatory cytokine productions by cervical epithelial cells. In summary, the CE-OOC established an in vitro model that can recapitulate the ectocervical and the endocervical epithelial regions of the cervix. The established CE-OOC may become a powerful tool in obstetrics and gynecology research such as in studying cervical remodeling during pregnancy and parturition and the dynamics of cervical epithelial cells in benign and malignant pathology in the cervix.
AB - Damage to the cervical epithelial layer due to infection and inflammation is associated with preterm birth. However, the individual and/or collective roles of cervical epithelial layers in maintaining cervical integrity remain unclear during infection/inflammation. To determine the intercellular interactions, we developed an organ-on-chip of the cervical epithelial layer (CE-OOC) composed of two co-culture chambers connected by microchannels, recapitulating the ectocervical and endocervical epithelial layers. Further, we tested the interactions between cells from each distinct region and their contributions in maintaining cervical integrity in response to LPS and TNFα stimulations. The co-culture of ectocervical and endocervical cells facilitated cellular migration of both epithelial cells inside the microchannels. Compared to untreated controls, both LPS and TNFα increased apoptosis, necrosis, and senescence as well as increased pro-inflammatory cytokine productions by cervical epithelial cells. In summary, the CE-OOC established an in vitro model that can recapitulate the ectocervical and the endocervical epithelial regions of the cervix. The established CE-OOC may become a powerful tool in obstetrics and gynecology research such as in studying cervical remodeling during pregnancy and parturition and the dynamics of cervical epithelial cells in benign and malignant pathology in the cervix.
KW - cervical ripening
KW - cervix
KW - epithelial-to-mesenchymal transition
KW - organ-on-a-chip
KW - pregnancy
KW - preterm birth
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U2 - 10.1096/fj.202002590RRR
DO - 10.1096/fj.202002590RRR
M3 - Article
C2 - 33689188
AN - SCOPUS:85102906073
SN - 0892-6638
VL - 35
JO - FASEB Journal
JF - FASEB Journal
IS - 4
M1 - e21463
ER -