Gibbons B H, Gibbons I R
J Cell Biol. 1980 Jan;84(1):13-27. doi: 10.1083/jcb.84.1.13.
Sperm flagella of the sea urchin Tripneustes gratilla beat with asymmetrical bending waves after demembranation with Triton X-100 in the presence of EGTA and reactivation at pH 8.1 with 1 mM ATP in the presence of 2 mM MgSO4. Addition of 0.1--0.2 mM free Ca2+ to these reactivated sperm induces 70--95% of them to become quiescent. This quiescence can be reversed by reduction of the free Ca2% concentration with EGTA, or by dilution to reduce the MgATP2- concentration below 0.3 mM. The quiescent waveform is characterized by a sharp principal bend of approximately 5.6 rad in the proximal region of the flagellum, a slight reverse bend in the midregion that averages approximately 0.3 rad, and a principal bend of approximately 1.1 rad in the tip. The quiescent sperm are highly fragile mechanically, and disruption, including microtubule sliding, occurs spontaneously at a slow rate upon standing or immediately upon gentle agitation. Mild digestion by trypsin causes a gradual appearance of normal, symmetrical flagellar beating. Addition of increasing concentrations of vanadate to quiescent sperm causes a graded decrease in the proximal bend angle, with 50 micrometers vanadate reducing it to approximately 2.6 rad. In the presence of 0.1 mM free Ca2% and 10 micrometers vanadate, a characteristic, crescented stationary bend is induced in the demembranated sperm, without intermediate oscillatory beating, by the addition of either 0.1 or 1 mM ATP. In the absence of vanadate, these two concentrations of ATP produce asymmetric beating and quiescence, respectively. The results support the hypothesis that quiescence in live sperm is induced by an elevated concentration of intracellular Ca2%. In addition, they demonstrate that bending can occur in flagella in which oscillatory beating is inhibited and emphasize the close relationship between asymmetric beating and quiescence.
在用Triton X-100在EGTA存在下对海胆(Tritneustes gratilla)精子进行去膜处理,并在2 mM MgSO4存在下于pH 8.1用1 mM ATP重新激活后,其鞭毛以不对称弯曲波摆动。向这些重新激活的精子中添加0.1 - 0.2 mM游离Ca2+会导致70 - 95%的精子静止。这种静止状态可通过用EGTA降低游离Ca2+浓度,或通过稀释使MgATP2-浓度降至0.3 mM以下来逆转。静止波形的特征是鞭毛近端区域有一个约5.6弧度的尖锐主弯曲,中部区域有一个平均约0.3弧度的轻微反向弯曲,末端有一个约1.1弧度的主弯曲。静止的精子在机械上非常脆弱,在静置时或轻轻搅拌后会自发地以缓慢速率发生包括微管滑动在内的破坏。用胰蛋白酶轻度消化会使正常的对称鞭毛摆动逐渐出现。向静止精子中添加浓度不断增加的钒酸盐会导致近端弯曲角度逐渐减小,50微摩尔钒酸盐可将其降至约2.6弧度。在存在0.1 mM游离Ca2+和10微摩尔钒酸盐的情况下,通过添加0.1或1 mM ATP,可在去膜精子中诱导出一种特征性的新月形静止弯曲,而无中间振荡摆动。在没有钒酸盐的情况下,这两种浓度的ATP分别产生不对称摆动和静止。这些结果支持了活精子中的静止是由细胞内Ca2+浓度升高诱导的这一假设。此外,它们表明在振荡摆动受到抑制的鞭毛中也能发生弯曲,并强调了不对称摆动和静止之间的密切关系。