Complementary tissue-specific expression of LIF and LIF-receptor mRNAs in early mouse embryogenesis.

Abstract:

:The maintenance of pluripotential embryonic stem (ES) cells is dependent on the cytokine LIF. This report documents the mRNA expression profiles of LIF and the two components of the LIF-receptor complex, LIF-R and gp130, during early mouse embryogenesis. These mRNAs were undetectable in 1- or 2-cell embryos, but all were present by the blastocyst stage. LIF transcripts were localised in the differentiated trophectoderm, and were absent from the pluripotential inner cell mass. In contrast, LIF-R mRNA was found in the inner cell mass but not in the trophectoderm. This complementary pattern of expression is suggestive of a paracrine coupling between stem cells and differentiated progeny at the earliest stage of mammalian development. After implantation, transcripts for all components were down-regulated in the embryo. High levels of LIF-R and gp130 mRNAs were observed in the deciduum, however. These dynamic, tissue-specific expression patterns are consistent with regulatory roles for LIF or related cytokines, both in the maintenance of pluripotency in the mouse embryo, and in development of the foeto-maternal interface.

journal_name

Mech Dev

authors

Nichols J,Davidson D,Taga T,Yoshida K,Chambers I,Smith A

doi

10.1016/0925-4773(96)00531-x

subject

Has Abstract

pub_date

1996-07-01 00:00:00

pages

123-31

issue

2

eissn

0925-4773

issn

1872-6356

pii

092547739600531X

journal_volume

57

pub_type

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