TY - JOUR
T1 - Microspike-mediated particle transport towards the cell body during early spreading of 3T3 cells
AU - Albrecht-Buehler, G.
AU - Goldman, R. D.
N1 - Funding Information:
The work reported in this paper was undertakend ur-ing the tenure of a Research Training Fellowship awarded to G. Albrecht-Buehler by the International Agency for Research on Cancer. The scanning electron microscopew as provided by an equipmentg rant from the NSF. R. D. Goldman is supportedb y grants from the NSF and the ACS.
PY - 1976/2
Y1 - 1976/2
N2 - Freshly trypsinized 3T3 cells send out microspikes of 0.2 μm diameter and up to 10 μm length within 20 min after attachment to a glass substratum. The microspikes move actively and eventually attach to the substratum. Subsequently, lamellae flow out between lines of attached microspikes. If, however, colloidal gold particles of 0.2-0.4 μm diameter and clusters of gold particles up to 4 μm in diameter are placed on the substratum and a microspike attaches to them, we observed two reactions of the microspikes to this contact. They either retract upon contact, transporting the attached particles to the cell surface at a speed of 0.2 μm/sec, or the particles flow toward the cell body while the microspike stays in place. This action results in the clearing of a circular area around each spreading cell before lamellae flow out. "Clearing" proceeds at serum concentrations between 1 and 20% and in concentrations of colchicine up to 20 μm/ml. In concentrations of cytochalasin B higher than 5 μg/ml, however, particle removal is completely inhibited, although the microspikes are still produced by the cell. Transmission electron microscopy shows that the microspikes contain mostly longitudinally oriented microfilaments and only a few microtubules, if any.
AB - Freshly trypsinized 3T3 cells send out microspikes of 0.2 μm diameter and up to 10 μm length within 20 min after attachment to a glass substratum. The microspikes move actively and eventually attach to the substratum. Subsequently, lamellae flow out between lines of attached microspikes. If, however, colloidal gold particles of 0.2-0.4 μm diameter and clusters of gold particles up to 4 μm in diameter are placed on the substratum and a microspike attaches to them, we observed two reactions of the microspikes to this contact. They either retract upon contact, transporting the attached particles to the cell surface at a speed of 0.2 μm/sec, or the particles flow toward the cell body while the microspike stays in place. This action results in the clearing of a circular area around each spreading cell before lamellae flow out. "Clearing" proceeds at serum concentrations between 1 and 20% and in concentrations of colchicine up to 20 μm/ml. In concentrations of cytochalasin B higher than 5 μg/ml, however, particle removal is completely inhibited, although the microspikes are still produced by the cell. Transmission electron microscopy shows that the microspikes contain mostly longitudinally oriented microfilaments and only a few microtubules, if any.
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U2 - 10.1016/0014-4827(76)90624-8
DO - 10.1016/0014-4827(76)90624-8
M3 - Article
C2 - 1248523
AN - SCOPUS:0017261673
SN - 0014-4827
VL - 97
SP - 329
EP - 339
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 2
ER -