Johannes A Eble Editor

Donald Gullberg has a BSc in Chemistry from Uppsala University Sweden and gained his PhD on a thesis entitled "Structural and functional characterization of collagen receptors on primary rat hepatocytes and cardiac fibroblasts” in 1990 under the supervision of Prof. Kristofer Rubin at the Department of Medical and Physiological Chemistry. During 1990-1992 both he and Marion Kusche-Gullberg conducted postdoctoral research with Professors John and Lisa Fessler at Molecular Biology Institute, UCLA. In his laboratory the ITGA11 was identified and characterized in 1990´s. He was appointed to a professorship at University of Bergen Department of Biomedicine in 2004 and has continued to study ITGA11 in the context of tissue and tumor fibrosis. He has spent two inspiring sabbaticals at UCSF (with Prof., MD Dean Sheppard 2010-2011, with Prof. PhD Valerie Weaver 2017-2018). 

After having studied biochemistry at the University of Tübingen, Johannes A. Eble gained an intense training on extracellular matrix and collagen-binding integrins during his doctorate thesis at the Max Planck-Institute of Biochemistry in Martinsried close to Munich. In 1994, he gained his doctorate degree from the Ludwig Maximilians-University, Munich, under the Prof. Dr. Klaus Kühn’s supervision. During 1995-1998, he intensified his knowledge of integrins under Prof. Martin Hemler’s supervision at the Dana Faber-Cancer Institute of Harvard Medical School in Boston, where he developed the technique of recombinant expression of soluble integrins, especially of the laminin-332-binding ITGA3 integrin. After his return to Germany, he habilitated at the University of Münster in 2004. In 2008, he was appointed to a professorship of vascular matrix biology at the University of Frankfurt within the Excellence Cluster Cardio-Pulmonary System. Since 2014, he heads the Institute of Physiological Chemistry and Pathobiochemistry of the University of Münster. Although his scientific focus still pivots around integrins, his view on cell adhesion and migration has widened to integrin agonists and antagonists, the former being recombinant integrin-binding mini-collagen and mini-laminin-332, the latter being integrin-blocking snake venom toxins. Moreover, redox regulation of integrins and cell-matrix contacts is also included in his research portfolio.