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Max-Born-Institut Berlin (MBI)

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Fig 46.<br />

Effect of mean blood flow velocity in venules on the growth rate constant<br />

(s-1) of white bodies: results from seventeen experiments. Diameter<br />

of the venules (in µm) : open circles 40-49; left half filled 50-<br />

59; right half filled 60-69; closed circle > 70.<br />

24<br />

<strong>Max</strong> <strong>Born</strong> • Gustav <strong>Born</strong><br />

Fig 47.<br />

Growth rate constant of platelet thrombi as a<br />

function of blood flow velocity. (from Richardson,<br />

P. D., (1973). Nature (Lond.), 245, 103-<br />

104).<br />

understanding of cell mechanics, particularly through knowledge of the membrane channels<br />

that transport ions, of other transmembrane structures that transmit information (receptor<br />

signalling) and of cytoskeletal components that link to these structures, we have come to<br />

recognise the enormity of the co-ordinated processes responsible for the state of a cell at any<br />

given instant. Thus, so much needs to be known about a cell at any moment to be able to predict<br />

changes in its state that at present we do not have methods which might provide the information<br />

without disturbing what the cell would do if we did not interrogate its current state”<br />

(Richardson, 2004).<br />

Ion channels permit the selective exchange of sodium and potassium across cell membranes<br />

otherwise impermeable to these ions. The channels are complicated, selective structures with<br />

gates which are open and shut by chemical activators. Each gate is in one of two states, open<br />

or shut. Only the numbers of open and shut gates are statistically measurable, not the state of<br />

the individual gate. Another statistical phenomenon is the quantal release of the neurotransmitter<br />

acetyl choline from small vesicles inside nerve endings [41]. Quantal release is individually<br />

demonstrable but not predictable, and measurable only when occurring together in lar-

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