Understanding the critical cellular events that define synchrony between the developing embryo and the maternal uterus in a species that is phylogenetically related to humans will be paramount in improving the success of assisted reproductive therapies. Ongoing studies in the Fazleabas laboratory are at the leading edge of this type of research endeavor. His laboratory was the first to conclusively demonstrate that signals from the primate embryo, like those of other species, induce cell specific changes in uterine gene expression. These changes are thought to play critical roles in establishing a synchrony between the maternal environment and the developing embryo that is a pre requisite for a successful pregnancy. These studies have clearly elucidated the mechanisms by which apoptosis is inhibited within the uterus in the presence of a conceptus, the fundamental hormonal and cellular requirements associated with the process of decidualization and potential functions of uterine proteins in the establishment of pregnancy. A hallmark of all the studies from his laboratory is the ability to confirm all their in vitro findings in vivo as a fundamental application of true physiology in the appropriate tissue context. In addition, his laboratory has established a baboon model for endometriosis. The focus of these studies are to understand the etiology and pathophysiology of Endometriosis, a poorly understood, enigmatic disease that affects five to fifteen percent of all women of reproductive age and has an estimated economic impact of approximately 22 billion dollars in the US. It is reported to be the leading cause of infertility in women. The unique nature of the primate model that he has developed to study endometriosis and the strong multidisciplinary group that he has established has led to important and fundamental findings regarding the causative effects of endometriosis on aberrant gene expression in the eutopic endometrium that may contribute to infertility. Furthermore, studies from the. Fazleabas' laboratory has also identified the genes that may be involved with the process of angiogenesis and cell adhesion during the establishment of lesions in the peritoneal environment.
Research Technologist I
Joshi, Niraj, PhD
Niraj Joshi, Ph.D. received his undergraduate, masters’ and doctoral education in Zoology (Reproductive Biology) from the The M. S. University of Baroda in India. He completed his postdoctoral resarch under the supervision of Dr. Asgi Fazleabas on Epigenetic and Molegular Regulation of Endometriosis. He is now an Assistant Professor in the Department of Obstetrics, Gynecology and Reproductive Biology. His research focuses on understanding the role of miRNAs in regulating cell cycle, inflammation and progesterone resistance in endometriosis using baboon model and human clinical samples.
Research Asst/Lab Manager
Mark Olson received his BS degree in Cell and Molecular Biology from the University of Illinois at Urbana- Champaign. He is responsible for the overall daily management of the laboratory and all animal protocols. His research focus is on developing mouse xenograft models to study cell ‚Äìcell interactions during the development of endometriosis.
Research Technologist I