Actin Organization in Cells Responding to a Perforated Surface, Revealed by Live Imaging and Cryo-Electron Tomography

被引:46
作者
Jasnin, Marion [1 ]
Ecke, Mary [1 ]
Baumeister, Wolfgang [1 ]
Gerisch, Guenther [1 ]
机构
[1] Max Planck Inst Biochem, Klopferspitz 18, D-82152 Martinsried, Germany
关键词
ARP2/3; COMPLEX; LISTERIA-MONOCYTOGENES; SELF-ORGANIZATION; MOTILE CELLS; DICTYOSTELIUM; DYNAMICS; MICROSCOPY; WAVES; PROTEIN; MYOSIN;
D O I
10.1016/j.str.2016.05.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In a 3D environment, motile cells accommodate their protruding and retracting activities to geometrical cues. Dictyostelium cells migrating on a perforated film explored its holes by forming actin rings around their border and extending protrusions through the free space. The response was initiated when an actin wave passed a hole, and the rings persisted only in the PIP3-rich territories surrounded by a wave. To reconstruct actin structures from cryo-electron tomograms, actin rings were identified by cryo-correlative light and electron microscopy, and thin wedges of relevant regions were obtained by cryo-focused ion-beam milling. Retracting stages were distinguished from protruding ones by the accumulation of myosin-II. Early actin rings consisted of filaments pointing upright from the membrane, entangled with a meshwork of filaments close to the membrane. Branches identified at later stages suggested that formin-based nucleation of filaments was followed by Arp2/3-mediated network stabilization, which prevented buckling of the force-generating filaments.
引用
收藏
页码:1031 / 1043
页数:13
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