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ULTIMATE COMPUTING - Quantum Consciousness Studies

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112 Cytoskeleton/Cytocomputer<br />

lymphocytes and macrophages are white blood cells which combat infection by<br />

migrating from the blood stream into an open wound to engulf invading bacteria<br />

or foreign material. Cells of developing embryos perform precisely<br />

choreographed movements that give rise to different tissues. Internal movement<br />

such as the streaming of cytoplasm, secretion of cell product vesicles (i.e.<br />

neurotransmitters), engulfment of matter, and the separation of paired<br />

chromosomes in cell division are routine functions whose complexity,<br />

organization, and precision generally boggle biologists.<br />

Also, well controlled muscle contraction which depends on the<br />

conformational bending of myosin head molecules can result in strenuously<br />

running a 4 minute mile, or delicately painting a Mona Lisa. Four categories of<br />

cytoplasmic movement and force generation will be considered with attention to<br />

their regulatory mechanisms. These are: cytoplasmic probing, bending sidearms,<br />

ciliary and collective movements, and geodesic tensegrity structures.<br />

5.5.1 Cytoplasmic Probing<br />

In the early 20th century, W. H. Lewis, an embryologist at Carnegie Institute<br />

of Washington, took time lapse motion pictures of cells grown in culture<br />

(Lazarides and Revel, 1979). Lewis treated the fibroblasts (active cells which<br />

repair wounds) with protein cleaving enzymes to break up adhesive contacts and<br />

networks of extracellular material holding the cells together. He separated the<br />

resulting clumps and grew individual cells in a nutrient medium. After a few<br />

hours, Lewis’ fibroblasts had acquired a polygonal shape. Along the shortest side<br />

of the polygon were lamellipodia, delicate sheet-like extensions of the cytoplasm.<br />

He exclaimed: “the ruffled lamellipodia slowly bend back and forth like the<br />

ruffles of a dress in a slight breeze” (Lazarides and Revel, 1979). Later, Ingram<br />

and Abercrombie at University College London studied the membrane coated<br />

ruffled lamellipodium, fibroblasts’ main locomotion organ. The lamellipodium<br />

forms strings and contacts with the substrate on which the cell rests, stretching<br />

portions of the rest of the cell among several temporary adhesions. When the cell<br />

is spread out to its fullest extent it maintains one or two primary ruffles, each of<br />

which tend to lead the cell in a particular direction. The cell then migrates with<br />

changes in direction which typically come at intervals of several hours. If a ruffle<br />

does not stick and the cell move in another direction, the ruffle folds back on the<br />

upper surface of the cell, collapses onto it and disappears into the cell (Figure<br />

5.22, 5.23 and 5.24).

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