Daniel A. Kirschner
professor of biology
Ph.D., Harvard University
Fields of Interest
Structural biochemistry/neurobiology; ultrastructural neuropathology of and adhesive mechanisms in CNS and PNS myelins; fibrillogenesis and molecular organization of amyloid assemblies; remyelination; spinal cord injury; Alzheimer's disease; prion diseases.
Our current research interests are focused in two areas: the structure and dynamic membrane interactions in abnormal nerve myelin, in which alterations have resulted from experimental, pathological, or genetic conditions; and the molecular organization of amyloid, which are deposits of mis-folded polypeptides involved in certain neurodegenerative diseases (including Alzheimer's disease, Huntington's disease and prion diseases) and in systematic amyloidoses. To link structure and composition at the molecular, macromolecular and tissue levels in the nervous system, our studies in these two areas utilize x-ray diffraction, microscopy at the light and ultrastructural levels, a variety of protein and lipid biochemical techniques, and molecular modeling.
What holds myelin together, and how are its constituents targeted in diseases? To characterize the molecular organization of lipids and proteins in nerve myelin membranes, and to define the molecular interactions of its membrane arrays, we are correlating biophysical and biochemical results from different types of specimens (e.g., whole unfixed or fixed tissue from a phylogenetic range of vertebrates, tissue homogenates, tissue fractions and model lipid/protein systems). Among the questions we are addressing: how does the organization of proteins and lipids in myelin account for the inter-membrane interactions of the membranes? What is the structural basis of demyelination? Our findings are relevant to understanding the process of membrane disruption and delamination which occurs in demyelinating diseases such as multiple sclerosis and certain peripheral neuropathies. Our current focus is on understanding how specific mutations in myelin adhesion proteins or in lipid biosynthetic pathways affect the stability and functionality of the myelin.
What is the process by which proteins or their fragments self-assemble to form potentially cytotoxic amyloid deposits? The molecular organization of paired helical filaments, amyloid plaque cores and cerebrovascular amyloid isolated from Alzheimer's disease (AD) brain are being studied using a variety of structural techniques. High-resolution x-ray fiber patterns and electron microscopic images are being obtained from in vitro assemblies of synthetic polypeptides homologous with AD amyloid. Determining the dimensions and spatial organization of the structural units that comprise paired helical filaments, AD amyloids and related in vitro assemblies from prion diseases and from other amyloidoses will illuminate our understanding of their formation, interrelationships and stability, and will provide insight on how they might be related to or derive from normally occurring cellular components. These findings are also relevant to the general problem of protein folding. Current efforts are directed at developing a novel screen for assessing whether or not specific compounds can inhibit amyloid formation, and if so, by what mechanism.
“@ & Between the Nodes: What X-rays & Neutrons Reveal About Nerve Myelin”, Invited talk, IBMC, Porto, Portugal (5/9)
“Nerve Myelin Between the Nodes: What X-rays & Neutrons Reveal“, invited speaker, A.I. DuPont Hospital for Children, Nemours Translational Science Research Seminar Series, Wilmington, Delaware (10/25)
“Neutron Diffraction from Myelin: Redux >Forty Years”, invited speaker, Symposium: “Structural Dynamics and Dynamical Structures: Future and Challenges of Neutron Scattering in Biology”, Institute Laue-Langevin, Grenoble, France (10/3-10/5).
“Novel Molecular Views of Nerve Myelin Using Microbeam X-ray Diffraction and Neutron Diffraction”, invited talk, American Crystallographic Association, annual meeting, Boston (7/30).
“Myelin Structural Biology: Molecular Organization and Dynamic Interactions”, Symposium on Membrane Biology, invited lecture, Acibadem University Medical School, Istanbul, Turkey (5/30)
“A Sabbatical Report: Advances in Structural Biology: My Adventures in Milano & Grenoble with X-rays & Neutrons, i Gelati & les Croissants, Ciao & Bonjour”, seminar, Biology Dept, BC (11/1)
“Nerve Myelin: A New Rap On An Old Wrap – Pushing the Boundaries of Analysis”, invited seminar, Department of Physiology and Biophysics, Boston University (10/18)
“New Raps on A Phylogenetically Old Wrap: From Molecules to Myelinopathies”, invited lecture at the BioCenter Oulu Doctoral Programme Advanced Course in Structural Biology, University of Oulu, Oulu, Finland (5/31)
“En(w)raptures of Myelin”, invited lecture in “Protein Structure & Disease”, Brandeis University (3/28)
“Assessing Myelin Development and Structure in Animal Models of Human Disorders “ Istituto di Richerche Farmacologiche Mario Negri”, Milano, Italy (10/11)
“Structure Determination by X-ray Diffraction”, invited lecture in Biological Chemistry (Bi435), Boston College (4/30)
Ahmed SS, Li H, Cao C, Sikoglu EM, Denninger AR, Su Q, Eaton S, Liso A, Xie J, Szucs S, Zhang H, Moore C, Kirschner DA, Seyfried TN, Flotte TR, Matalon R, and Gao G (2013) A single intravenous rAAV injection as late as P20 achieves efficacious and sustained CNS gene-therapy in Canavan mice. Molecular Therapy, Jul 2. doi: 10.1038/mt.2013.138. [Epub ahead of print].
Patzkó A, Bai Y, Saporta MA, Katona I, Wu XY, Wrabetz L, Feltri ML, Wang S, Dillon LM, Kamholz J, Kirschner DA, Sarkar F, Shy ME (2012) Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice. Brain 135:3551-66. doi: 10.1093/brain/aws299.
Saporta MAC, Shy BR, Patzko A, Bai Y, Pennuto M, Ferri C, Tinelli E, Saveri P, Kirschner DA, Crowther M, Southwood C, Gow A, Wu X, Feltri ML, Wrabetz L, Shy ME (2012) MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth 1B. Brain 135:2032-2047. doi: 10.1093/brain/aws140.
Jiang H, Kiebish MA, Kirschner DA, Han X (2012) Multi-dimensional mass spectrometry-based shotgun lipidomics and its application for analysis of PEX7 mouse brain lipidome. In Lipidomics – Technologies and Applications (K Ekroos, ed.), Wiley-VCH, Weinheim, Germany.
Gilardini A, Avila RA, Luckett R, Lu J, Oggioni N, Rodruguez-Menendez V. Bossi M, Canta A, Cavaletti G, Kirschner DA (2012) Myelin structure is unaltered in chemotherapy-induced peripheral neuropathy. NeuroToxicology 33:1-7. doi: 10.1016/j.neuro.2011.10.010.
Echeverria V, Zeitlin R, Burgess S, Patel S, Barman A, Thakur G, Mamcarz M, Wang L, Sattelle DB, Kirschner DA, Mori T, Leblanc R, Prabhakar R, and Arendash GW (2011) Cotinine reduces amyloid-b aggregation and improves memory in Alzheimer’s mice. J Alz Dis 23:1-19. (link to PubMed abstract).
Avila RA, Inouye H, Feltri ML, Wrabetz L, Kirschner DA (2010) P0 (protein zero) mutation Ser34Cys underlies instability of internodal myelin in S63C mice. J Biol Chem, Oct 11. 285(53):42001-12.
Inouye, H., Gleason, K.A., Decatur, S.M., Kirschner, D.A. 2010. Differential effects of Phe19 and Phe20 on fibril formation by amyloidogenic peptide Aβ16-22 (Ac-KLVFFAE-NH2). Proteins: Structure, Function, and Bioinformatics 78: 2306–2321.
Kirschner, D.A., Avila, R.L., Luoma, A., Enzmann, G.U., Agrawal, D., Inouye, H., Bunge, M.B., Kocsis, J.D., Peters, A., Whittemore, S. 2010. Rapid assessment of internodal myelin integrity in CNS tissue. Journal of Neuroscience Research 88: 712–723.
Verheijen, M.H., Camargo, N., Nadra, K., de Preux, A.-S., Verdier, V., Luoma, A.M., Crowther, M., Inouye, H., Shimano, H., Chen, S., Brouwers, J., Helms, B.J., Feltri, M.L., Wrabetz, L., Kirschner, D.A., Chrast, R., Smit, A.B. 2009. SREBP cleavage activation protein (SCAP) is required for dynamic synthesis of a proper Schwann cell myelin membrane. Proceedings of the National Academy of Sciences of the United States of America 106: 21383–8.
Agrawal, D., Hawk, R., Avila, R.L., Inouye, H., Kirschner, D.A. 2009. Internodal myelination during development quantitated using x-ray diffraction. Journal of Structural Biology 168: 521–526.
Kirschner, D.A., Karthigesan, J., Bizzozero, O.A., Kosaras, B., Inouye, H. 2009. Myelin structure and composition of myelinated tissue in the African lungfish. Neuron Glia Biology 4: 59–70.
Inouye, H., and Kirschner, D.A. 2008. Myelin: A one-dimensional biological “crystal” for x-ray and neutron scattering. In: Molecules: Aggregation, Nucleation, Crystallization — Beyond Medical and Other Implications (Eds. J. Sedzik, P. Riccio), World Scientific Publishing, Singapore.
Flores, A.I., Narayanan, S.P., Morse, E., Shick, H.B., Avila, R.L., Kirschner, D.A., and Macklin, W.B. 2008. Constitutively active Akt induces myelination in the central nervous system. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience 28: 7174–83.
Kirschner, D.A., Gross, A.A., Hidalgo, M., Inouye, H., Gleason, K., Abdelsayed, G., Castillo, G.M., Snow, A.D., Pozo-Ramajo, A., Petty, S.A., and Decatur, S.M. 2008. Fiber diffraction as a screen for amyloid inhibitors. Current Alzheimer Research 5: 288–307.
Luo, X.Y., Cerullo, J., Dawli, T., Priest, C., Haddadin, Z., Kim, A., Inouye, H., Suffoletto, B.P., Avila, R.L., Lees, J.P., Sharma, D., Xie, B., Costello, C.E., and Kirschner, D.A. 2008. Peripheral myelin of Xenopus laevis: role of electrostatic and hydrophobic interactions in membrane compaction. Journal of Structural Biology 162: 170–183.
Luo, X., Inouye, H., Sharma, D., Lee, D., Avila, R.L., Salmona, M., and Kirschner, D.A. 2007. Cytoplasmic domain of zebrafish myelin P0: adhesive role depends on beta-conformation. Biophysical Journal 93: 3515–3528.
Luo, X.Y., Sharma, D., Inouye, H., Lee, D., Avila, R.L., Salmona, M., and Kirschner, D.A. 2007. Cytoplasmic domain of human myelin P0 likely folded as beta-structure in compact myelin. Biophysical Journal 92: 1585–1597.
Avila, R.A., Tevlin, B.R., Lees, J.P., Inouye, H., and Kirschner, D.A. 2007. Myelin structure and composition in zebrafish. Neurochemical Research 32: 197–209.
Yin, X., Baek, R.C., Kirschner, D.A., Peterson, A., Fujii, Y., Nave, K.A., Macklin, W.B., and Trapp, B.D. 2006. Evolution of a neuroprotective function of central nervous system myelin. Journal of Cell Biology 172: 469–478.
Wrabetz, L., D’Antonio, M., Pennuto, M., Dati, G., Tinelli, E., Fratta, P., Previtali, S., Imperiale, D., Zielasek, J., Toyka, K., Avila, R.A., Kirschner, D.A., Messing, A., Feltri, M.L., and Quattrini, A. 2006. Different intracellular pathomechanisms produce diverse MPZ-neuropathies in transgenic mice. Journal of Neuroscience 26: 2358–2368.
Inouye, H., Sharma, D., Goux, W.J., and Kirschner, D.A. 2006. Structure of core domain of fibril-forming PHF/tau fragments. Biophysical Journal 90: 1774–1789.
Shinchuk, L. M., Sharma, D., Blondelle, S.Y., Reixach, N., Inouye, H., and Kirschner, D.A. 2005. Poly(L-alanine) expansions form core beta-sheets that nucleate amyloid assembly. Proteins: Structure, Function, and Bioinformatics 61: 579–589.
Sharma, D., Shinchuk, L.M., Inouye, H., Wetzel, R., and Kirschner, D.A. 2005. PolyGlutamine homopolymers having 8-45 residues form slab-like beta-crystallite assemblies. Proteins: Structure, Function, and Bioinformatics 61: 398–411.
Avila, R.A., Inouye, H., Baek, R., Yin, X., Trapp, B.D., Feltri, M.L., Wrabetz, L., and Kirschner, D.A. 2005. Structure and stability of internodal myelin in mouse models of hereditary neuropathy. Journal of Neuropathology & Experimental Neurology 64: 976–990.
Kirschner, D.A., Wrabetz, L., and Feltri, M.L. 2004. The P0 Gene. In: Myelin Biology and Disorders 1, (Ed. R.A. Lazzarini et al.), Elsevier/Academic Press, NY, pp. 523–545.
Inouye, H., Bond, J.E., Deverin, S.P., Lim, A., Costello, C.E., and Kirschner, D.A. 2002. Molecular organization of amyloid protofilament-like assembly of betabellin 15D: Helical array of beta-sandwiches. Biophysical Journal 83: 1716–1727.
Thompson, A.J., Cronin, M.S., and Kirschner, D.A. 2002. Myelin protein zero (P0) exists as dimers and tetramers in native membranes of Xenopus laevis peripheral nerve. Journal of Neuroscience Research 67(6): 766–771.