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IMV Executive Assistant

email: virology@umn.edu

tel. (612) 624-1926

fax. (612) 625-1108

 

18-242 Moos Tower
515 Delaware St. SE
Minneapolis, MN 55455

General Questions:

virology@umn.edu

Kim Carpenter Mansky,
Associate Professor

Developmental and Surgical Sciences, School of Dentistry

Phone: (612) 626-5582

Email:kmansky@umn.edu

Education

B.S., University of North Carolina - Chapel Hill
Ph.D., University of Wisconsin - Madison
Postdoctoral Research: Ohio State University

Research Interests

Bone biology and bone cancer; Osteoimmunology; Bone metabolic disorders associated with HIV infection and antiretroviral therapy

Bone is often thought to be a tissue that does not change once it is formed. However, bone is very dynamic and is constantly being remodeled. In healthy individuals, bone formation and resorption are in balance. Osteoporosis, which affects ten million people in the United States and puts at risk another thirty-four million Americans, is a result of the uncoupling of bone formation and resorption. Other diseases such as breast and prostate cancer or multiple myeloma cause changes in bone density indirectly through the action of tumor cells. Women with advanced breast cancer almost always develop bone metastases. Bone metastases are usually associated with bone pain and an increase in the susceptibility to fractures thought to be a result of the breakdown of bone caused by the presence of tumor cells. Other diseases such as rheumatoid arthritis can also result in bone loss.  Our lab has general interests in the cell signaling between the two types of bone cells that are involved in bone remodeling – osteoblasts (i.e., cells that form bone) and osteoclasts (i.e., cells that resorb bone) – and how perturbation of this signaling can lead to bone or bone-associated disease.

Osteoimmunology studies the interface and crosstalk between the skeletal and immune systems.  In particular, osteoimmunology studies the shared components and mechanisms between the two systems, which include the ligands, receptors, signaling molecules and transcription factors.  The bone marrow is important for the proper development of the immune system, and has important stem cells that maintain the immune system. Cytokines produced by immune cells (e.g., RANKL, M-CSF, TNFa, interleukins and interferons) can also have important effects on regulating bone homeostasis. The balance between bone modeling and remodeling can be perturbed during chronic inflammation, which can lead to bone metabolic disorders as well as bone pain.  We have a particular interest in osteoimmunology as it relates to rheumatoid arthritis, HIV infection, and periodontal disease.

Metabolic disorders associated with highly active antiretroviral therapy (HAART) regimens are becoming increasingly important in the chronically HIV-infected population that has access to therapy.  Clinical observations have revealed a strong correlation of bone density loss in HIV-infected individuals during HAART, particularly in conjunction with the antiretroviral drug tenofovir – a nucleotide analog that inhibits HIV reverse transcriptase. We are interested in understanding how tenofovir affects bone mineral density and to apply this knowledge for the identification of biomarkers and for developing adjuvant therapies to reduce bone mineral density loss during HAART.

 

Selected Recent Publications

  • Mansky, KC, Jensen, ED, Davidova, J, Yamamoto, M, Gopalakrishnan, R. 2013. Protein kinase D promotes in vitro osteoclast differentiation and fusion. Journal of Biological Chemistry 288:9826-9834.
  • Billington, CJ, Fiebig JE, Forsman CL, Pham L, Burbach N, Sun M, Jaskoll T, Mansky K, Gopalakrishnan R, O'Connor MB, Mueller TD, Petryk A. 2011. Glycosylation of twisted gastrulation is required for BMP binding and activity during craniofacial development. Frontiers in Physiology 2:59
  • Pham, L., Kaiser, B., Romsa, A., Schwarz, T., Gopalakrishnan, R., Jensen,
    E.D., and Mansky, K.C. 2011. HDAC3 and HDAC7 have opposite effects on
    osteoclast differentiation. Journal of Biological Chemistry 286:12056-65.
  • Pham, L., Beyer, K., Jensen, E., Rodriguez, J.S., Davydova, J., Yamamoto, M., Petryk, A., Gopalakrishnan, R., and Mansky, K.C. 2011. Bone morphogenetic protein 2 signalling in osteoclasts in negatively regulated by the BMP antagonist, twisted gastrulation. Journal of Cellular Biochemistry 112:793-803.
  • Mansky, K.C.  2010.  Aging, human immunodeficiency virus, and bone health.  2010.  Clinical Interventions in Aging, 5:285-292.
  • Schwarz, T., Murphy, S., Sohn, C., and Mansky, K.C.  2010.  C-TAK1 interacts with micropthalmia-associated transcription factor, Mitf, but not the related family member Tfe3.  Biochemical and Biophysical Research Communications, 394:890-895.
  • Grigsby, I.F., Pham, L., Mansky, L.M., Gopalakrishnan, R., Carlson, A. and Mansky, K.C. 2010.  Tenofovir treatment of primary osteoblasts alters gene expression profiles: implications for bone mineral density loss. Biochemical and Biophysical Research Communications, 394:48-53.
  • Schwarz, T., Sohn, C., Kaiser, B., Murphy, S., Jensen, E.D., Gopalakrishnan, R. and Mansky, K.C.  2010.  The 19S proteosomal lid subunit POH1 enhances the transcriptional activity of  Mitf in osteoclasts.  Journal of Cellular Biochemistry, 109:967-974.
  • Jensen, E.D., Pham, L., Billington, C.J., Espe, K., Carlson, A.E., Westendorf, J.J., Petryk A., Gopalakrishnan, R., and Mansky, K.C.  2010.  Bone Morphogenetic Protein 2 Directly Enhances Differentiation of Murine Osteoclast Precursors.  Journal of Cellular Biochemistry 109:672-682.
  • Grigsby,I.F., Pham, L., Gopalakrishnan, R., Mansky, L.M., and Mansky, K.C.  2010.  Downregulation of Gnas, Got2 and Snord32a following tenofovir exposure of primary osteoclasts.  Biochemical and Biophysical Research Communications 391:1324-1329.
  • Grigsby, I.F., Pham, Lan, Mansky, L.M, Gopalakrishnan, R., and Mansky, K.C. 2009.  Tenofovir-associated bone density loss.  Therapeutics and Clinical Risk Management. 6:41-47.
  • Rodriguez, J.S., Mansky, K.C., Jensen, E.D., Carlson, A., Schwarz, T., Pham, L., MacKenzie, B., Prasad, H., Rohrer, M.D., Petryk, A. and Gopalakrishan, R. 2009.   Enhanced osteoclastogenesis causes osteopenia in Twisted gastrulation-deficient mice. Journal of Bone and Mineral Research 24:1917-26.
  • Suttamanatwong, S., Jensen, E.D., Schilling, J., Franceschi, R.T., Carlson, A.E., Mansky, K.C. and Gopalakrishnan, R.  2009.  Sp proteins and Runx2 mediate regulation of matrix gla protein (MGP) expression by parathyroid hormone.  Journal of Cellular Biochemistry 15:284-92.
  • Sharma, S.M., Bronisz A., Hu, R., Patel K., Mansky, K.C., Sif, S., and Ostrowski, M.C.  2007. MITF and PU.1 recruit p38 MAPK and NFATc1 to target genes during osteoclast differentiation.  Journal of Biological Chemistry 282:15921-15929.
  • Bronisz A, Sharma SM, Hu R, Godlewski J, Tzivion G, Mansky KC, Ostrowski
    MC. 2006. Microphthalmia-associated transcription factor interactions with
    14-3-3 modulate differentiation of committed myeloid precursors. Mol Biol
    Cell. 17:3897-906.
  • Wei G, Schaffner AE, Baker KM, Mansky KC, Ostrowski MC. 2003. Ets-2
    interacts with co-repressor BS69 to repress target gene expression. Anticancer Research 23:2173-8.
  • Mansky, K.C., Sankar, U., Han, J., and Ostrowski, M.C. 2002. Microphthalmia transcription factor (MITF) is a target of p38 MAP kinase pathway in response to RANK ligand signaling. JBC 277:11077-11083.
  • Mansky, K.C., Sulzbacher, S., Purdom, G., Nelsen, L., Hume,D.A., Rehli, M. and Ostrowski, M.C. 2002. The microphthalmia transcription factor and the related helix-loop-helix factors TFE-3 and TFE-C collaborate to activate the tartrate-resistant acid phosphatase promoter. Journal of Leukocyte Biology 71: 304-310.
  • Mansky, K.C., Marfatia, K., Purdom, G., Luchin, A., Hume, D.A., and Ostrowski, M.C.2002. The microphthalmia transcription factor (MITF) contains two N-terminal domains required for transactivation of osteoclast target promoters and rescue of mi mutant osteoclasts. Journal of Leukocyte Biology 71; 295-303.

 

 

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'Wisc-e-sota', a Joint UMN-UW Virology Training Grant Symposium was first held on Friday, Sepbember 20th, 2013 at the Uniiversity of Wisconsin-La Crosse, Cartwright Center. This was the inaugural collaborative symposium of the NIH T32-supported virology training programs at the University of Wisconsin-Madison and the University of Minnesota-Twin Cities. Talks and poster sessions were presented by students, postdocs and faculty. The second UMN-UW Virology Training Grant Symposium will be held in the Fall 2014. Details to follow.

The 2014 IMV Symposium will be held on May 12, 2014 and Mark Denison (Vanderbilt) and Bert Semler (UC-Irvine) will be the Keynote Speakers. Click on the link below to register and submit abstracts.

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