| Literature DB >> 25430742 |
Chizuru Ito1, Kenji Yamatoya2, Kiyotaka Toshimori3.
Abstract
The acrosome is a Golgi-derived sperm cell organelle enclosed by a continuous acrosomal membrane. The acrosomal membrane complexes with surrounding matrices containing molecules necessary for fertilization; however, the complex of acrosomal membrane and associating matrices (CAMAM) has not been visualized in detail under living conditions. Here, we analyzed the CAMAM at the nanometer level using super-resolution stimulated emission depletion (STED) fluorescence microscopy and equatorin-enhanced green fluorescent protein transgenic mice. The STED images were compared with the corresponding images taken by immunoelectron microscopy. Consequently, the substructure of CAMAM could be differentiated at nanometer-scale resolution by STED microscopy without the need for sectioning. The information obtained in this study will be beneficial not only for understanding the molecular mechanism of fertilization but also for cell imaging under living conditions.Entities:
Keywords: CLSM; Eqtn-EGFP transgenic mouse; STED microscopy; complexity of sperm acrosomal membrane; conventional high-resolution microscopy; immunoelectron microscopy
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Year: 2014 PMID: 25430742 DOI: 10.1093/jmicro/dfu101
Source DB: PubMed Journal: Microscopy (Oxf) ISSN: 2050-5698 Impact factor: 1.571