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Nm23/NDP kinases in human male germ cells: role in spermiogenesis and sperm motility?

Nucleoside diphosphate (NDP) kinases, responsible for the synthesis of nucleoside triphosphates and produced by the nm23 genes, are involved in numerous regulatory processes associated with proliferation, development, and differentiation. Their possible role in providing the GTP/ATP required for sperm function is unknown. Testis biopsies and ejaculated sperm were examined by immunohistochemical and immunofluorescence microscopy using specific antibodies raised against Nm23-H5, specifically expressed in testis germinal cells and the ubiquitous NDP kinases A to D. Nm23-H5 was present in sperm extract, together with the ubiquitous A and B NDP kinases (but not the C and D isoforms) as shown by Western blotting. Nm23-H5 was located in the flagella of spermatids and spermatozoa, adjacent to the central pair and outer doublets of axonemal microtubules. High levels of NDP kinases A and B were observed at specific locations in postmeiotic germinal cells. NDP kinase A was transiently located in round spermatid nuclei and became asymmetrically distributed in the cytoplasm at the nuclear basal pole of elongating spermatids. The distribution of NDP kinase B was reminiscent of the microtubular structure of the manchette. In ejaculated spermatozoa, the proteins presented specific locations in the head and flagella. Nm23/NDP kinase isoforms may have specific functions in the phosphotransfer network involved in spermiogenesis and flagellar movement.

Antibody Specificity↗

A comparison of time, temperature, and refreezing variables on frozen sperm motility recovery.

OBJECTIVE: To compare motility recovery among methods of thawing semen in serial freeze-thaw processes. DESIGN: A comparison of treatments. SETTING: Semen cryobank laboratory. PARTICIPANTS: Semen samples from an existing cryobank. INTERVENTIONS: Portions of each of 35 ejaculates were thawed serially in either a 37 degrees C water bath for 10 minutes or at room temperature for 30 minutes. Motility was estimated, and the samples were immediately refrozen. Thaws were performed initially (T1), at 24 hours (T2), and at 1 week (T3). MAIN OUTCOME MEASURE: Percent motility. RESULTS: The initial motility of all samples averaged 73.2%. Serial thaws at 37 degrees C yielded mean motility recoveries of 34.0%, 21.8%, and 8.3% for T1, T2, and T3, respectively. Those at room temperature were 22.4%, 7.9%, and 1.3%. Motilities progressively decreased from initial to final thaw regardless of temperature. Semen thawed at 37 degrees C had a higher motility recovery at all thaw times compared with samples thawed at room temperature. CONCLUSIONS: For sperm frozen rapidly in liquid nitrogen and for sperm subjected to multiple freeze-thaw processes, motility recovery is improved if thaw is carried out at 37 degrees C versus room temperature.

Cryopreservation↗

Sperm motility.

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Alcoholism↗