Afzelius B A
Department of Ultrastructure Research, The Wenner-Gren Institute, Stockholm University, Sweden.
Int J Dev Biol. 1995 Oct;39(5):839-44.
The finding of men with living but immotile sperm tails has initiated a search for the cause of the disorder. The sperm tails were found to lack dynein arms or to have some other ultrastructurally visible defect and the cilia were found to have the same defects. The disorder was hence named the immotile-cilia syndrome. Two more groups with the same clinical symptoms were later found, characterized by ciliary dysmotility or ciliary aplasia. In each group there are several subgroups. Many of the affected persons have situs inversus totalis; in some subgroups the incidence of situs inversus is probably 50%; there is, thus, a random determination of visceral asymmetry. Five hypotheses have been forwarded that attempt to explain the connection between ciliary defects and loss of laterality control. Support for, or evidence against, these five hypotheses have been sought in some animal models of the syndrome. Whereas immotile-cilia syndrome in dogs and pigs is very similar to the human one, an animal model in the rat differs from the human syndrome in that mainly the males are affected. Two animal models in the mouse differ in that one has ciliary defects but no increased incidence of situs inversus and the other has a random determination of visceral laterality and no ciliary defects. The connection between ciliary defects and random determination of laterality remains enigmatic.
发现存在存活但精子尾部不动的男性后,人们开始寻找这种病症的病因。研究发现精子尾部缺少动力蛋白臂或存在其他超微结构可见的缺陷,并且纤毛也有同样的缺陷。因此,这种病症被命名为不动纤毛综合征。后来又发现了另外两组具有相同临床症状的病例,其特征为纤毛运动障碍或纤毛发育不全。每组中又有几个亚组。许多患者患有完全性内脏反位;在一些亚组中,内脏反位的发生率可能为50%;因此,内脏不对称是随机确定的。已经提出了五种假说,试图解释纤毛缺陷与左右控制丧失之间的联系。人们在该综合征的一些动物模型中寻找对这五种假说的支持或反对证据。狗和猪的不动纤毛综合征与人类的非常相似,而大鼠的动物模型与人类综合征的不同之处在于主要是雄性受到影响。小鼠中的两种动物模型的不同之处在于,一种有纤毛缺陷但内脏反位的发生率没有增加,另一种内脏左右侧是随机确定的且没有纤毛缺陷。纤毛缺陷与左右侧随机确定之间的联系仍然是个谜。