## Abstract The frequent use of some rare earths in the medical and industrial domains make us worry about their intracellular behavior into the body. Reason for which we have investigated the subcellular localization of one of these elements, the samarium, in the mammary gland of lactating female
Identification and function of neonatal Fc receptor in mammary gland of lactating mice
β Scribed by Petru Cianga; Corneliu Medesan; James A. Richardson; Victor Ghetie; E. Sally Ward
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 446 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0014-2980
No coin nor oath required. For personal study only.
β¦ Synopsis
In addition to its proposed function in regulating serum IgG levels, the MHC class I-related neonatal Fc receptor (FcRn) is known to play a role in IgG transfer across rodent yolk sac and neonatal intestine. In contrast to humans, for which transplacental transfer of IgG appears to be the only mechanism of maternal IgG delivery, the transmission of IgG in mice occurs both antenatally (yolk sac) and neonatally (transport from mother's milk across intestinal epithelial cells). In the current study, a possible role for FcRn in regulating IgG transfer into milk has been investigated. FcRn has been shown to be present in functional form in the mammary gland of lactating mice, and is localized to the epithelial cells of the acini. Analysis of the transfer of Fc fragments and IgG which have different affinities for FcRn indicate that, unexpectedly, these proteins are transferred in inverse correlation with their binding affinity for FcRn. Thus, in the lactating mammary gland FcRn appears to play a role in recycling IgG in a mode that may have relevance to FcRn trafficking during the maintenance of constant serum IgG levels.
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## Abstract We have previously described pluripotent, parityβinduced mammary epithelial cells (PIβMEC) marked by Rosa26βlacZ expression in the mammary glands of parous females. PIβMEC act as lobuleβlimited epithelial stem/progenitor cells. To determine whether parity is necessary to generate PIβMEC