Timothy Springer, Ph.D.
Latham Family Professor
Department of Biological Chemistry and Molecular Pharmacology
Department of Medicine
Harvard Medical School
Program in Cellular and Molecular Medicine
Division of Hematology
Department of Medicine
Boston Children’s Hospital
- Contact Information
- Office Phone: 617.713.8200
- Fax: 617.713.8232
- Email: timothy.springer at childrens.harvard.edu
- Administrative Assistant
- Maggie Nielsen
- Phone: 617.713.8225
- Email: margaret.nielsen at childrens.harvard.edu
We work on receptor-ligand interactions and signal transmission across membranes. Graduate students and postdoctoral fellows find my lab fascinating because of the wide range of structural, cell biological, and single molecule techniques that we use. Some areas that currently fascinate us follow.
How are conformational signals transmitted across membranes in integrins, over long distances between the distal ligand-binding domains and cytoplasmic domains, and how is integrin activation coordinated with the actin cytoskeleton to mediate cell migration? How do G proteins and kinases activate integrins (inside-out signaling) so they can bind to extracellular ligands and cytoskeletal proteins, to coordinate adhesion and directional cell migration and mediate inside-out and outside-in signaling? How is integrin activation confined to lamellipodia? We have proposed that a mechanism for coordinating binding to ligands outside the cell and the cytoskeleton inside the cell is inherent in integrin structure and the allosteric pathways that relate the bent - closed headpiece; extended- closed headpiece; and extended – open headpiece conformations. Cell biological experiments are required to test this hypothesis.
How do representative members of the integrin family work? This family is quite diverse, and we study representative integrins including LFA-1, Mac-1, αXβ2, α4β1, and α4β7on leukocytes, aIIbb3on platelets, and the aV integrins that bind and activate TGF-β. To gain a broad overview, we may extend to other subfamilies including those that recognize collagen and laminin.
How can integrins, depending on their activation state, mediate transient adhesion that supports rolling, or alternatively, firm adhesion, in postcapillary venules? This question is being addressed with integrins α4β1, α4β7, and their ligands MAdCAM-1, and VCAM-1, which mediate both lymphocyte homing in the vasculature and cell adhesion and immune responses in tissues. Furthermore, we are examining how small drug-candidate molecules and antibodies in the clinic for asthma, multiple sclerosis, and inflammatory bowel disease bind to these integrins.
We have initiated single molecule laser tweezer measurements for understanding the mechanobiology of cell adhesion and diverse physiologic processes including hemostasis and thrombosis. How can adhesion molecules such as integrins and selectins resist substantial forces that should break receptor-ligand noncovalent bonds? Does the fact that many adhesion receptors have high affinity conformations that are more extended than the low affinity conformation along the cell attachment site - ligand binding site axis give them a mechanical advantage in resisting force? Can we measure this using novel receptor-ligand constructs with laser tweezers or the atomic force microscope? Does von Willebrand factor sense shear in the bloodstream and activate hemostasis because extension reveals otherwise hidden receptor binding sites?
One new area of research in the lab is von Willebrand factor and mutations that cause the important bleeding diathesis, von Willebrand disease. We are pursuing single molecule experiments, functional assays, electron microscopy, and crystallography to understand the complex mechanobiology of VWF, which is the largest soluble protein in the body and functions as a shear sensor in the vasculature to arrest arteriolar bleeding. The conformation of VWF, its binding to ligands on the vessel wall and on platelets, and its cleavage by ADAMTS13 are regulated by shear.
A second new area is malaria. We posit that the structures of important vaccine targets will reveal both interesting biology, and enable rational development of vaccines. These vaccines will focus the immune response on conserved epitopes, and avoid masking by polymorphic epitopes that pathogens often use to evade immune responses. Proteins on sporozoites are candidates for vaccines that prevent infection. We are interested in determining the structure of the sheath that surrounds sporozoites, its main component the circumsporozoite protein, and the motility protein TRAP. Proteins on gametocytes are targets for vaccines that prevent Plasmodium fertilization and infection in mosquitoes, and prevent transmission to other humans. These proteins include a family unique to Apicomplexans with 6-Cys domains, and HAP2, a putative gamete fusogen conserved in many eukaryotic phyla.
A third new area is TGF-β signaling, which regulates development, wound healing, immune responses, and tumour-cell growth and inhibition. Latent TGF-β and receptors for active TGF-β are ubiquitous; it is activation of TGF-β in the extracellular space that limits activity. Recently, we have determined a structure of latent TGF-β1 that reveals how the latency associated peptide (LAP), a 250 residue prodomain, shields the 110 residue growth factor and participates in its activation through interactions with αV integrins and latent TGF-β binding proteins (LTBPs). We also have studied how a different cell surface protein called GARP becomes disulfide linked to latent TGF-β, and presents it for activation by integrins αVβ6 and αVβ8 that are expressed on immune cells, and bind to an RGD motif in LAP. We believe that yet another cell surface molecule that presents latent TGF-β remains to be discovered. Furthermore, we are interested in understanding how other TGF-βs are activated, particularly TGF-β2, which lacks the RGD integrin-binding motif in its LAP sequence. A wide range of projects, all the way from knockout mice to structure determination, are in the offing.
Finally, we always strive to make connections between basic research and disease. In the past, we have found inherited defects of integrins in leukocyte adhesion deficiency, ICAM-1 as the cellular receptor for rhinovirus, and SDF-1 as the natural ligand for the HIV coreceptor CXCR4. Our discoveries of LFA-1 and LFA-3 resulted in the drugs efalizumab (Raptiva, LFA-1 antibody, Genentech) and alefacept (Amevive, LFA-3-Fc fusion protein, Biogen). We are currently developing and characterizing antibodies specific for the activated conformation of integrin I domains as therapeutics for autoimmune disease. Our work has important implications for development and improvement of therapeutics directed to many receptors.
Dr. Springer graduated from the University of California, Berkeley, and earned a Ph.D. in molecular biology and biochemistry from Harvard University. He is a member of the National Academy of Sciences and the American Academy of Arts and Sciences. In 2004, he was co-recipient of the prestigious Crafoord Prize given by the Royal Swedish Academy of Sciences.