Reproductive Parameters of Female Mice Transgenic for Over-expresssion of CCL2 Poster with Audio | Discuss via ZoomBiology
By: Cora Thompson
Faculty Sponsor: Karin Bodensteiner
Chemokine ligand 2 (CCL2) is an inflammatory chemokine involved in non-viral immune responses. Mice transgenic for CCL2 under control of human glial fibrillary acidic protein (GFAP) overexpress CCL2 in astrocytes as well as the hypothalamus and ovaries. Ovarian expression of CCL2 is greatest during ovulation, the time of greatest inflammation. CCL2 has also been implicated in human ovarian pathophysiology. Thus, mice transgenic for overexpression of CCL2 may serve as a model system for understanding how CCL2 impacts ovulatory processes and ovulatory pathophysiology. To investigate differences in pregnancy rates, offspring number, and pup survivability between wild-type and transgenic females (n=12 per group), adult females 55-67 days of age were caged with wild-type males for 14 days. Number of pregnancies, total number of offspring, and number of surviving pups did not differ between groups. However, pup weight change (as a measure of lactation performance) did differ between groups on postnatal days 4, 5, 6, 8, 9, 10, 11, and 12 (p ≤ 0.05). In addition, time to sexual maturation was delayed in transgenic female offspring (p = 0.004), but proportion of time dams spent in diestrus, proestrus, estrus, and metestrus did not differ between groups. To measure ovulatory capacity, ovaries were removed on diestrus, fixed in neutral buffered formalin, embedded in paraffin, serially sectioned at 8µm, and stained with Hematoxylin and Eosin. Data analysis on number of corpora lutea is ongoing, but as we did not observe a difference in number of offspring, we do not expect number corpora lutea to differ.