Keith Roberts Porter

Keith Roberts Porter (June 11, 1912 – May 2, 1997) was a Canadian- American cell biologist. He created pioneering biology techniques and research using electron microscopy of cells. Porter also contributed to the development of other experimental methods for cell culture and nuclear transplantation. He was also responsible for naming the endoplasmic reticulum, conducting work on the 9 + 2 microtubule structure in the axoneme of cilia, and coining the term " microtrabecular lattice." In collaborations with other scientists, he contributed to the understanding of scellular structures and concepts such as compartmentalization, flagella, centrioles, fibrin, collagen, T-tubules and sarcoplasmic reticulum. He also introduced microtome cutting

Early life and education

Keith Porter was born in Yarmouth, Nova Scotia, on June 11, 1912, the son of Aaron and Josephine Roberts Porter. He finished his undergraduate program at Acadia University in 1934, and became a graduate student at Harvard University. At Harvard, he earned a doctorate (Ph.D.) for his work on frog embryo development in 1938. Following this degree, he married Katherine Elizabeth Lingley, a former student at Acadia University. They had one son, Gregory, who died just over one year later. Starting in the early 1940s, he conducted research at The Rockefeller Institute for Medical Research in New York. He eventually became a citizen of the United States in 1947.

Career/research

In 1939, Porter was a research assistant at The Rockefeller Institute for Medical Research under James B. Murphy, a cancer researcher. Porter his early work in Murphy's lab on the effect of carcinogens on embryonic development of rat embryos. Because it was difficult for the these cells to fix properly to the slide, Porter concluded that osmium tetroxide preserved the cells the best.Satir, P. (1997). Keith R. porter and the first electron micrograph of a cell. ''Endeavour, 21''(4), 169-171. When Porter micro-graphed the first cell, he noticed that only the thin sections could be seen. The nuclei region was a dark blob due to all the internal structures surrounding the nucleus. He needed a higher penetration power to see the thicker portions of the cell. Only small sections of thinly sliced cells were able to be micro-graphed, so Porter turned his attention to developing a way that whole cells could be photographed. In conjunction with Joseph Blum, he designed an ultramicrotome section of specific tissue thickness to allow the electron microscope to penetrate these cells. By 1956, he became a professor and full member at the Rockefeller University.

From 1961 to 1967, Porter returned to Harvard University and was chair of the biology department (1965–1967). Porter's research at Harvard concerned the sarcoplasmic reticulum and T system; he conducted this work in collaboration with Clara Franzini-Amstrong. He then explored the role of microtubules in motility, cell division, and control of cell shape with Lewis Tilney, J. Richard McIntosh, and Ursula Goodenough-Johnson.

In 1968, Porter left to work as chair of the new Department of Molecular, Cellular, and Developmental Biology at the University of Colorado Boulder. Porter spearheaded a laboratory dedicated to a higher voltage (1000 kV) electron microscope that improved the ability to examine the interior of cells by virtue of its high penetrating power. When he retired, at age 70, the university awarded him an honorary degree and renamed "his" building Porter Biosciences.

Porter became a professor at University of Maryland, Baltimore County in 1984 before joining Peachey Lee's laboratory at the University of Pennsylvania in 1988, post-retirement. UMBC's Keith R. Porter Core Imaging Facility is dedicated to Porter.

Porter helped found the American Society for Cell Biology

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