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Fig. 5b: QF-DE of ciliary axonemes showing axonemal dynein arms and spokes

A. The outer dynein arms along the A subfiber appear as globular units attached to the microtubule by stem-like connections. The ciliary membrane was removed during the preparation and the axoneme was probably in rigor so that all dyneins are bound to the adjacent doublet. EM taken on 5/6/88 by C. Schroeder with Zeiss 10A TEM. Neg. 40,500X. Bar = 50nm. B. QF-DE of a portion of an isolated cilium exposing two rows of outer dynein arms arising from subfiber A of each doublet. The heavy chains of the dynein complex are linked to the microtubule by stems (arrow) that can be seen in this micrograph. Thin protrusions (arrowhead) link the dynein heavy chains to the adjacent doublet. Much of this cilium is still covered by the ciliary membrane (cm). EM Taken on 6/7/88 by C. Schroeder with Zeiss 10A TEM. Neg. 19,800X. Bar = 0.1µm. C. QF-DE of another segment of the edge of the axoneme showing the outer axonemal dynein arms that extend from the A-subfiber of a doublet to bind to the B subfiber of the adjacent doublet (for cross-sectional details of a cilium, see Chaper 11, figure 21). EM taken on 4/21/88 by C. Schroeder with Zeiss 10A TEM. Neg. 31,500X. Bar = 0.1µm. D. QF-DE of an isolated and longitudinally fractured cilium exposing the middle of the cilium. The spokes extending from the doublets toward the two singlet microtubules (see Chapter 11, figure 21) are viewed. These spokes are spaced unevenly so they appear to be arranged into triplets (brackets). The fracture plane, while in general is longitudinal, exposes the singlets and outer doublets at different levels so various periodicities appear along these microtubules. The cilium may also be slightly twisted along its length. EM taken on 2/15/88 by C. Schroeder with Zeiss 10A TEM. Neg. 31,500X. Bar = 0.1µm.
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