Rousseaux-Prévost R, Lesur P, Collier F, Rigot J M, Dalla Venezia N, Pol P S, Delaunay J, Gauthier A, Rousseaux J
Institut de Recherches sur le Cancer, Lille.
Lancet. 1994 Mar 26;343(8900):764-5. doi: 10.1016/s0140-6736(94)91840-6.
Molecular defects responsible for morphologically abnormal spermatozoa (teratospermia) associated with male sterility are largely unknown. We report defective expression of protein 4.1, a cytoskeletal protein initially recognised in red cells. In some patients with severely amorphous sperm heads, protein 4.1 had an abnormal sub-cellular localisation (tail instead of head) and appeared as high-molecular-weight isoforms, especially a 135 kDa species instead of the 82 kDa isoform seen in fertile sperm. Because the 135 kDa isoform is characteristic of immature germ cells from testis, its presence in teratospermia suggests profoundly disturbed sperm differentiation.
与男性不育相关的形态异常精子(畸形精子症)的分子缺陷在很大程度上尚不明确。我们报告了蛋白质4.1的表达缺陷,该蛋白质是一种最初在红细胞中被识别的细胞骨架蛋白。在一些精子头部严重无定形的患者中,蛋白质4.1具有异常的亚细胞定位(位于尾部而非头部),并呈现为高分子量异构体,尤其是一种135 kDa的异构体,而非在可育精子中所见的82 kDa异构体。由于135 kDa异构体是睾丸未成熟生殖细胞的特征,其在畸形精子症中的存在表明精子分化受到严重干扰。