The Fluorescence-Activated Cell Sorting/Flow Cytometry Shared Resource Laboratory (FACS/FCMSRL) is and will continue to be a state ofthe art facility to collaborate to provide analytical fluorescence-based flow cytometry and cell sorting. It will serve investigators from laboratories associated with the Thematic Focus of the COBRE, from other laboratories in the University of Nevada School of Medicine (UNSOM), from laboratories in the other Colleges of the University of Nevada Reno (UNR) and from other public and private laboratories in the area. To meet these overall objectives, there are several activities that will be performed. First, the FACS/FCMSRL will continue and extend existing activities which include the following: 1) assisting in designing, executing and analyzing flow cytometric experiments, 2) titrating and testing labeled antibodies and 3) providing laboratory and classroom training in flow cytometry. Second, the FACS/FCMSRL will work with investigators in the Thematic Focus and in the Single Cell Molecular Expression (SCME) laboratory to identify and initiate the characterization of subsets of cells in smooth muscle tissues. These cells include hematopoietic cells, smooth muscle cells, interstitial cells of Cajal, fibroblast-like cells, neuronal cells and mesothelial-like cells. Third, the Director will continue to monitor developments in flow cytometry by continuing to participate in the activities of the International Society for the Advancement of Cytometry (ISAC) by attending regular meetings and Congresses of ISAC and by participating in other ISAC-sponsored activities. Existing instruments will be upgraded as appropriate and additional instruments will be purchased if needed. Finally, during the period ofthe Phase III funding, mechanisms to provide long-term sustainability will be developed.
It is essential for a research university to have state ofthe art flow cytometry (FCM) and fluorescence activated cell sorting (FACS) capabilities. The investigators in Physiology &Cell Biology (PCB) have been at the forefront in using FCM and FACS to characterize the cells in smooth muscle tissues. These studies will now be extended by working with the new equipment in the Single Cell Molecular Expression Laboratory.
|Zhang, Xudong; Cozen, Aaron E; Liu, Ying et al. (2016) Small RNA Modifications: Integral to Function and Disease. Trends Mol Med 22:1025-1034|
|Scurry, Alexandra N; Heredia, Dante J; Feng, Cheng-Yuan et al. (2016) Structural and Functional Abnormalities of the Neuromuscular Junction in the Trembler-J Homozygote Mouse Model of Congenital Hypomyelinating Neuropathy. J Neuropathol Exp Neurol 75:334-46|
|Perrino, Brian A (2016) Calcium Sensitization Mechanisms in Gastrointestinal Smooth Muscles. J Neurogastroenterol Motil 22:213-25|
|Yuan, Shuiqiao; Schuster, Andrew; Tang, Chong et al. (2016) Sperm-borne miRNAs and endo-siRNAs are important for fertilization and preimplantation embryonic development. Development 143:635-47|
|Heredia, Dante J; Schubert, Douglas; Maligireddy, Siddhardha et al. (2016) A Novel Striated Muscle-Specific Myosin-Blocking Drug for the Study of Neuromuscular Physiology. Front Cell Neurosci 10:276|
|Peri, Lauren E; Koh, Byoung H; Ward, Grace K et al. (2015) A novel class of interstitial cells in the mouse and monkey female reproductive tracts. Biol Reprod 92:102|
|Lee, Haeyeong; Koh, Byoung H; Yamasaki, Evan et al. (2015) UTP activates small-conductance Ca2+-activated K+ channels in murine detrusor PDGFRÎ±+ cells. Am J Physiol Renal Physiol 309:F569-74|
|Berner, Vanessa K; duPre, Sally A; Redelman, Doug et al. (2015) Microparticulate Î²-glucan vaccine conjugates phagocytized by dendritic cells activate both naÃ¯ve CD4 and CD8 T cells in vitro. Cell Immunol 298:104-14|
|Yuan, Shuiqiao; Qin, Weibing; Riordan, Connor R et al. (2015) Ubqln3, a testis-specific gene, is dispensable for embryonic development and spermatogenesis in mice. Mol Reprod Dev 82:266-7|
|Oliver, Daniel; Yuan, Shuiqiao; McSwiggin, Hayden et al. (2015) Pervasive Genotypic Mosaicism in Founder Mice Derived from Genome Editing through Pronuclear Injection. PLoS One 10:e0129457|
Showing the most recent 10 out of 13 publications