During the initial stages of fertilization envelope elevation in eggs of Strongylocentrotus pur puratus and S. droebachiensis a large concavity of the egg cortex was observed in the light microscope. This concavity corresponded in shape and size with the elevating fertilization envelope. However, after the vitelline layers of eggs were disrupted and the eggs inseminated, the concavity failed to develop although the eggs were fertilized and developed normally. We propose that the concavity is formed owing to increased hydrostatic pressure within the perivitelline space. To further support this hypothesis we measured total egg protein secreted during fertilization, and found that 98% was retained within the perivitelline space. Furthermore, 80% of the total protein was contributed by the hyaline layer. Presumably, colloidal osmotic pressure and/or hydration of fertilization product, trapped beneath the fertilization envelope, is responsible for increased hydrostatic pressure within the perivitelline space, and therefore promotes not only fertilization envelope elevation, but the cortical concavity as well.
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http://dx.doi.org/10.1111/j.1440-169X.1980.00821.x | DOI Listing |
J Exp Bot
November 2024
The School of Life Sciences, Anhui Agricultural University, Hefei, 230036, China.
In flowering plants, pollen grain must undergo a series of critical processes, including adhesion, hydration, and germination, which are dependent on the stigma, to develop a pollen tube. This pollen tube then penetrates the stigma to reach the internal tissues of pistil, facilitating the transport of non-motile sperm cells to the embryo sac for fertilization. However, the dry stigma, characterized by the absence of an exudate that typically envelops the wet stigma, functions as a multi-layered filter in adhesion, hydration, germination and penetration that permits the acceptance of compatible pollen or tubes while rejecting incompatible ones, thereby protecting the embryo sac from ineffective fertilization and maintaining species specificity.
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October 2024
Jiangxi Provincial Key Laboratory of Natural Active Pharmaceutical Constituents, Department of Chemistry and Bioengineering, Yichun University, Yichun, China.
Mammalian sperm are characterized as specialized cells, as their transcriptional and translational processes are largely inactive. Emerging researches indicate that Ca serves as a crucial second messenger in the modulation of various sperm physiological processes, such as capacitation, hyperactivation, and the acrosome reaction. Specifically, sperm-specific calcium channels, including CatSper, voltage-gated calcium channels (VGCCs), store-operated calcium channels (SOCCs), and cyclic nucleotide-gated (CNG) channels, are implicated in the regulation of calcium signaling in mammalian sperm.
View Article and Find Full Text PDFEMBO Rep
November 2024
Institute of Women, Children and Reproductive Health, Shandong University, 250012, Jinan, China.
CHK1 mutations could cause human zygote arrest at the pronuclei stage, a phenomenon that is not well understood at the molecular level. In this study, we conducted experiments where pre-pronuclei from zygotes with CHK1 mutation were transferred into the cytoplasm of normal enucleated fertilized eggs. This approach rescued the zygote arrest caused by the mutation, resulting in the production of a high-quality blastocyst.
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December 2024
Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, 7-1 Kioi-cho, Chiyoda-ku, Tokyo 102-8554, Japan.
Hum Gene Ther
September 2024
Department of Biomedicine, Aarhus University, Aarhus C, Denmark.
The invention of next-generation CRISPR/Cas gene editing tools, like base and prime editing, for correction of gene variants causing disease, has created hope for use in patients leading to wider clinical translation. To realize this potential, delivery vehicles that can ferry gene editing tool kits safely and effectively into specific cell populations or tissues are in great demand. In this review, we describe the development of enveloped retrovirus-derived particles as carriers of "ready-to-work" ribonucleoprotein complexes consisting of Cas9-derived editor proteins and single guide RNAs.
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