Transgenic and Chimeric Mouse Core

NIH RePORTER · NIH · P30 · $119,341 · view on reporter.nih.gov ↗

Abstract

The accelerating incidence of diabetes and metabolic disorders and the continuing high prevalence of endocrine disorders in the American population demands continued exploration of a broad array of corresponding mechanistic pathways, pathophysiologic sequelae, and potential therapeutic approaches. In many cases these investigations can be accomplished most efficiently using model systems established in intact animals. The use of mouse models in these pursuits is now well established for its power, feasibility, and enormous potential. Creation of such models, by directed alterations of the mouse genome, is an essential component of an overall research effort in diabetes, obesity, and metabolic disorders. The Transgenic and Chimeric Mouse Facility (TCMF) provides investigators of the University of Pennsylvania Diabetes and Endocrinology Research Center (DRC) with the ability to carry out these studies in a cost effective and efficient manner. The TCMF applies state-of-the-art equipment and technology by a group of dedicated and highly skilled technical staff to this effort. The major services of the Core include generation of transgenic mice by DNA pronuclear injection, creation of chimeric mice by ES cell blastocyst injections, direct genome mutation/editing/modifications by targeted endonuclease (TALEN and Crispr-CAS) technologies, assisted (in vitro) fertilization, cryopreservation, long-term cryostorage, and shipping of frozen embryos or sperm to/from other facilities. The Core uses multiple microinjection platforms, laser-assisted technologies, state-of-the-art cryopreservation of gametes and embryos, and in vitro fertilization based line re-derivation to facilitate these goals. The facility consists of a microinjection suite, an adjacent dedicated cage room, and an off-site and highly secure cryopreservation storage facility. All functions, from ordering services, to following workflow, to storing and sending out lines are on-line and can be monitored in real-time. These efforts contribute substantially to the overall productivity of the members of the DRC and enhance the strength and relevance of their studies to intact mammalian systems. This maximizes the applicability of these studies to human disease and to the expansion of therapeutic modalities.

Key facts

NIH application ID
10137229
Project number
5P30DK019525-45
Recipient
UNIVERSITY OF PENNSYLVANIA
Principal Investigator
STEPHEN Aaron LIEBHABER
Activity code
P30
Funding institute
NIH
Fiscal year
2021
Award amount
$119,341
Award type
5
Project period
1997-03-01 → 2022-03-31