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BOR - Papers in Press, published online ahead of print February 6, 2008.
Biol Reprod 2008, 10.1095/biolreprod.107.063305
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BIOLOGY OF REPRODUCTION 78, 883–887 (2008)
DOI: 10.1095/biolreprod.107.063305
© 2008 by the Society for the Study of Reproduction, Inc.


research-article

Murine Maternal Cell Microchimerism: Analysis Using Real-Time PCR and In Vivo Imaging1

Eric C. Su 3, Kirby L. Johnson 4, Hocine Tighiouart 5, and Diana W. Bianchi 2 4

Divisions of Newborn Medicine3 and Genetics,4 Department of Pediatrics, Floating Hospital for Children, and Institute for Clinical Research and Health Policy Studies,5 Tufts-New England Medical Center, Boston, Massachusetts 02111

ABSTRACT

In humans, maternal cells are present in the affected tissues of children with inflammatory myopathy, scleroderma, and neonatal lupus. It is unknown if maternal cell microchimerism (MCM) contributes to the pathology of disease. We sought to understand the factors that affect MCM to serve as a baseline for future mechanistic studies. Using a mouse model, we bred female mice transgenic for the luciferase (Luc) reporter gene to wild-type (WT) males. The WT offspring were sacrificed at various postnatal ages. DNA was extracted from multiple organs, and real-time PCR amplification was used to quantify Luc transgene as a marker for maternally derived cells. Sensitivity was one to two transgenic cells per 100 000 WT cells. MCM was noted in 85% of mice and 45% of tissues assayed. The average quantity of MCM was 158 maternal cells per 100 000 neonatal cells. The organs displaying the highest frequency and quantity of MCM were heart and lung (P < 0.001). Postnatal age up to 21 days did not appear to affect levels of MCM (P = 0.47), whereas increasing parity may increase levels of MCM. The data show that MCM is a common occurrence in healthy newborn mice, that it is present in their major organs, and that there are organ specific differences. This may represent differential migration of maternal cells or varying receptivity of specific fetal organs to microchimerism. Pregnancy history appears to play a role in maternal cell trafficking. The role of MCM in pregnancy and disease pathogenesis remains to be elucidated.

maternal cell microchimerism, materno-fetal trafficking, mouse, pregnancy, real-time PCR


FOOTNOTES

1Supported by NIH HD049469-03.

Correspondence: 2Diana W. Bianchi, Departments of Pediatrics, Obstetrics and Gynecology, Tufts-New England Medical Center, 750 Washington Ave., Boston, MA 02111. FAX: 617 636 1469; e-mail: dbianchi{at}tufts-nemc.org







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Copyright © 2008 by the Society for the Study of Reproduction.