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This version published online on February 8, 2007
Endocrinology, doi:10.1210/en.2006-1542
A more recent version of this article appeared on May 1, 2007
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*Substance via MeSH

Submitted on November 17, 2006
Accepted on January 26, 2007

Reporter expression, induced by a GH promoter-driven Cre recombinase (rGHp-Cre) transgene, questions the developmental relationship between somatotropes and lactotropes in the adult mouse pituitary gland

Raul M Luque, Geraldine Amargo, Shinya Ishii, Corrinne Lobe, Roberta Franks, Hiro Kiyokawa, and Rhonda D. Kineman*

Section of Endocrinology, Diabetes and Metabolism Department of Medicine, and Transgenic Production Service, Research Resources Center, University of Illinois at Chicago, Chicago Illinois; Research and Development Division, Jesse Brown Veteran's Administration Medical Center, Chicago Illinois; Sunnybrook and Women's College Health Sciences Centre, Toronto, Ontario, Canada; Department of Molecular Pharmacology & Biological Chemistry, Northwestern University Feinberg School of Medicine, Chicago Illinois

* To whom correspondence should be addressed. E-mail: Kineman{at}uic.edu.

This report describes the development and validation of the rGHp-Cre transgenic mouse that allows for selective Cre-mediated recombination of loxP-modified alleles in the GH-producing cells of the anterior pituitary. Initial screening of the rGHp-Cre parental line showed Cre mRNA was specifically expressed in the anterior pituitary gland of adult Cre+/- mice and cephalic extracts of e17 Cre+/- fetuses. Heterozygote rGHp-Cre transgenic mice were crossbred with Z/AP reporter mice to generate Cre+/-,Z/AP+/- offspring. In this model system, the GH promoter-driven, Cre-mediated recombination of the Z/AP reporter leads to human placental alkaline phosphatase (hPLAP) expression which serves to mark cells that currently produce GH, in addition to cells that would have differentiated from GH cells but currently do not express the GH gene. Double immunocytochemistry of adult male and female Cre+/-,Z/AP+/- pituitary cells revealed the majority (~99%) of GH-producing cells of the anterior pituitary also expressed hPLAP, while ACTH, TSH and LH-producing cells were negative for hPLAP, confirming previous reports that corticotropes, thyrotropes and gonadotropes develop independently of the somatotrope lineage. A small subset (~10%) of the PRL-producing cells was positive for hPLAP, consistent with previous reports showing lactotropes can arise from somatotropes during pituitary development. However, the fact that 90% of PRL-producing cells were negative for hPLAP suggests that the majority of lactotropes in the adult mouse pituitary gland develop independently of the somatotrope lineage. In addition to developmental studies, the rGHp-Cre transgenic mouse will provide a versatile tool to study the role of a variety of genes in somatotrope function and neoplastic transformation.




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