Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1997 May;42(5):1062-9.
doi: 10.1023/a:1018853506830.

Ontogenetic development and distribution of antibody transport and Fc receptor mRNA expression in rat intestine

Affiliations

Ontogenetic development and distribution of antibody transport and Fc receptor mRNA expression in rat intestine

M G Martín et al. Dig Dis Sci. 1997 May.

Abstract

The intestine of the suckling rat has the unique capacity of absorbing immunoglobulins from maternal milk. We investigated intestinal Fc receptor mRNA expression and the absorption of orally administered antibodies to delineate the ontogeny and tissue specificity of this transport system. Duodenal expression of Fc receptor mRNA was at maximum levels between 1 and 19 days of age, but was not detectable during fetal life and in animals after weaning. Along the horizontal axis of the intestine, FcRn mRNA expression was maximum in the proximal duodenum and declined gradually in distal bowel. Similarly, absorption of orally administered antibody was low shortly after birth, but reached maximum levels at 14 days of age. By the time of weaning, antibody uptake had almost completely ceased. These data further delineate the temporal and spatial nature of the intestinal immunoglobulin transport system, and represent additional examples of how the intestinal Fc receptor is transcriptionally regulated.

PubMed Disclaimer

References

    1. Nature. 1986 Dec 4-10;324(6096):408 - PubMed
    1. Gastroenterology. 1987 Jan;92(1):186-91 - PubMed
    1. Am J Physiol. 1987 Apr;252(4 Pt 1):G574-84 - PubMed
    1. J Immunol. 1993 Dec 1;151(11):6076-88 - PubMed
    1. Proc R Soc Lond B Biol Sci. 1956 May 29;145(919):170-8 - PubMed

Publication types

MeSH terms

LinkOut - more resources