||Audrey Minden, PhD
Department of Chemical Biology
Phone: (848) 445 5766
Fax: (732) 445-0687
PhD, University of Illinois at Chicago
BA, Colorado College, Colorado Springs, CO
PhD, University of Illinois at Chicago, College of Medicine, IL
Post-Doc, University of California at San Diego, CA
In order to survive and develop normally, eukaryotic cells must be able to respond to a variety of extracellular stimuli and in some cases adapt to adverse conditions. Exposure to certain extracellular stimuli can trigger cell growth and division, while some stimuli can induce other responses such as cell differentiation, changes in cell shape, or even programmed cell death. Small GTPases of the Ras superfamily serve as molecular switches which mediate responses to many types of extracellular stimuli. Our lab is interested in understanding how small GTPases integrate signals from extracellular stimuli and in turn induce various cellular changes in mammalian cells. A major focus is the Rho family of GTPases, which are a subset of the Ras superfamily. Members of the Rho family, including Cdc42, Rac, and Rho, were first identified as proteins that have key roles in regulating the organization of the actin cytoskeleton and thereby control cell shape, motility, and adhesion. Subsequently, the Rho GTPases were found to have other functions including the regulation of cell proliferation and activation of signal transduction pathways that lead to changes in gene expression patterns. When improperly regulated, the Rho GTPases also play key roles in oncogenic transformation and tumor invasiveness. This most likely reflects the fact that changes in cell shape, adhesion, and motility, all play an important part in the oncogenic process. Furthermore, the Rho GTPases have been found to regulate important cell cycle regulatory genes which may cause cells to enter into the cell cycle and proliferate.
One area of research in our laboratory has been the identification of new molecular targets for the Rho GTPases. We have cloned genes for two new protein kinases that bind to and get activated by Cdc42. Both of these protein kinases are members of the PAK family of serine/threonine kinases. We have found that one of these kinases, PAK4, mediates cytoskeletal and cell shape changes in response to Cdc42 activation. Importantly, we have also found that a constitutively active mutant of PAK4 can induce anchorage oncogenic independent growth in fibroblasts. This may be due in part to effects this protein has on cell adhesion. This is especially intriguing because anchorage independent growth is a key step in the oncogenic process, and activated Cdc42 has been shown to have a similar effect. Furthermore, inhibition of PAK4 expression blocks oncogenic transformation by oncogenic Dbl, which is a potent oncogene and an activator of Cdc42. We predict that PAK4 is a key player in the signaling pathway by which Rho GTPases regulate oncogenic transformation. Currently we are investigating the substrates for PAK4 that may be directly responsible for its functions.
The second gene encodes another member of the PAK family, PAK5, which is also a target for Cdc42. Unlike PAK4, however, which is ubiquitously expressed, PAK5 is expressed mostly in the brain. The regulation of cytoskeletal organization and cell shape are particularly important in neuronal cells, especially during development when neurons extend axons and dendrites and connections are made with target cells. Consistent with this, we have found that activated PAK5 promotes neurite outgrowth when it is overexpressed in a neuroblastoma cell line. Experiments are currently underway in our lab to determine whether PAK5 is indeed an important player in the process of neurite outgrowth. This involves further studies in cell lines as well as a mouse knockout project in which we are generating mice which are deficient in the PAK5 gene.
Finally, we are interested in studying the developmental functions of the Pak family of proteins. We have developed mouse knockouts of both Pak4 and Pak5. Pak4 knockout mice are embryonic lethal, indicating that this protein is important for early embryonic development. We are now in the process of developing conditional knockout mice, so that we can study the role for Pak4 in specific tissues, especially the brain, and at different developmental times. In contrast to Pak4, Pak5 knockout mice are viable and appear to be normal. Future work will involve crossing these knockout mice with other Pak knockout mice, to determine whether its functions overlap with those of other Pak family members.
Liu, Y., Xiao, H., Tian, Y., Nekrasova, T., Hao, X., Lee,
H.J., Suh, N., Yang, C.S., Minden, A. (2008) The Pak4 protein kinase plays a
key role in cell survival and tumorigenesis in athymic mice. Molecular Cancer
Nekrasova, T., Jobes, M.L., Tingh, J.H., Wagner, G.C., Minden, A. (2008)
Targeted disruption of the Pak5 and Pak6 genes in mice leads to deficits in
learning and locomotion. Developmental Biology. 322:95-108.
Tian, Y., Lei, L., Cammarano, M., Nekrasova, T., Minden, A. (2009) Essential
role for the Pak4 protein kinase in extraembryonic tissue development and
vessel formation. Mech Dev. 126: 710-720.
Wong, L.E., Reynolds, A.B., Dissanayaka, N., Minden, A. (2010) p120-catenin is
a binding partner and substrate for Group B Pak kinases”. J. Cell. Biochem.
Liu, Y., Chen, N., Cui, X., Zheng, X., Deng, L., Price, S., Karantza-Wadsworth,
V., and Minden, A. (2010) The protein kinase Pak4 disrupts mammary acinar
architecture and promotes mammary tumorigenesis. Oncogene. 29:5883-5894.
Tian, Y., Liang, L., Minden, A. (2011) A key role for Pak4 in proliferation and
differentiation of neural progenitor cells. Dev Biol. 353:206-216.
Nekrasova, T., and Minden, A. (2011) Pak4 is required for regulation of cell
cycle regulatory protein p21, and for control of cell cycle progression. J
Cell. Biochem. 112:1795-1806.