» Articles » PMID: 9275089

Activin is a Local Regulator of Human Cytotrophoblast Cell Differentiation

Overview
Journal Endocrinology
Specialty Endocrinology
Date 1997 Sep 1
PMID 9275089
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

Cytotrophoblast cells of the first trimester placenta are highly invasive when removed from villi and cultured in vitro. In vivo, however, only selected cytotrophoblast cells break through the overlying syncytiotrophoblast to form cytotrophoblast columns and ultimately invade the endometrium. To explore the role of paracrine growth factors in regulating cytotrophoblast development, we cultured explants of first trimester chorionic villi in vitro. Both activin and inhibin, as well as the activin binding protein follistatin, are produced by various trophoblast cells throughout pregnancy. We found that addition of activin-A, but not inhibin-A, stimulated the outgrowth of cytotrophoblast cells into the surrounding matrix. This outgrowth was characteristic of that observed in extravillous cytotrophoblast cells in vivo; it was accompanied by cell division within the proximal region of the cytotrophoblast outgrowth, synthesis of fibronectin, as well as the expression of markers characteristic of invasive cytotrophoblast cells, human leukocyte antigen-G and matrix metalloproteinase (MMP)-9. Activin also specifically induced the early expression of MMP-2 within villous cytotrophoblast cells. Addition of the activin binding protein, follistatin, blocked all of the effects of exogenous activin. The morphological and biochemical effects of activin were similar to those observed when signaling of endogenous transforming growth factor-beta was blocked. Interestingly, the latter effects were also reversed by the addition of follistatin. These data suggest that activin plays a local role in promoting cytotrophoblast column formation, likely by regulating the differentiation of villous cytotrophoblast into extravillous cytotrophoblast cells.

Citing Articles

The role of epigenetics in women's reproductive health: the impact of environmental factors.

Yu X, Xu J, Song B, Zhu R, Liu J, Liu Y Front Endocrinol (Lausanne). 2024; 15:1399757.

PMID: 39345884 PMC: 11427273. DOI: 10.3389/fendo.2024.1399757.


TGFβ signalling: a nexus between inflammation, placental health and preeclampsia throughout pregnancy.

Horvat Mercnik M, Schliefsteiner C, Sanchez-Duffhues G, Wadsack C Hum Reprod Update. 2024; 30(4):442-471.

PMID: 38519450 PMC: 11215164. DOI: 10.1093/humupd/dmae007.


Trophoblast Differentiation: Mechanisms and Implications for Pregnancy Complications.

Lawless L, Qin Y, Xie L, Zhang K Nutrients. 2023; 15(16).

PMID: 37630754 PMC: 10459728. DOI: 10.3390/nu15163564.


Similarities and differences in placental development between humans and cynomolgus monkeys.

Matsumoto S, Okamura E, Muto M, Ema M Reprod Med Biol. 2023; 22(1):e12522.

PMID: 37377753 PMC: 10292683. DOI: 10.1002/rmb2.12522.


Biochemical Screening for Fetal Trisomy 21: Pathophysiology of Maternal Serum Markers and Involvement of the Placenta.

Guibourdenche J, Leguy M, Pidoux G, Hebert-Schuster M, Laguillier C, Anselem O Int J Mol Sci. 2023; 24(8).

PMID: 37108840 PMC: 10146970. DOI: 10.3390/ijms24087669.