Microscopic Analysis of Nuclear Speckles in a Viviparous Reptile.
Jeniffer Acosta-CárdenasLuis Felipe Jiménez-GarciaSarai de Jesús Cruz-GómezAna Paulina Mendoza-von der BorchMaría de Lourdes Segura-ValdezPublished in: International journal of molecular sciences (2024)
Nuclear speckles are compartments enriched in splicing factors present in the nucleoplasm of eucaryote cells. Speckles have been studied in mammalian culture and tissue cells, as well as in some non-mammalian vertebrate cells and invertebrate oocytes. In mammals, their morphology is linked to the transcriptional and splicing activities of the cell through a recruitment mechanism. In rats, speckle morphology depends on the hormonal cycle. In the present work, we explore whether a similar situation is also present in non-mammalian cells during the reproductive cycle. We studied the speckled pattern in several tissues of a viviparous reptile, the lizard Sceloporus torquatus , during two different stages of reproduction. We used immunofluorescence staining against splicing factors in hepatocytes and oviduct epithelium cells and fluorescence and confocal microscopy, as well as ultrastructural immunolocalization and EDTA contrast in Transmission Electron Microscopy. The distribution of splicing factors in the nucleoplasm of oviductal cells and hepatocytes coincides with the nuclear-speckled pattern described in mammals. Ultrastructurally, those cell types display Interchromatin Granule Clusters and Perichromatin Fibers. In addition, the morphology of speckles varies in oviduct cells at the two stages of the reproductive cycle analyzed, paralleling the phenomenon observed in the rat. The results show that the morphology of speckles in reptile cells depends upon the reproductive stage as it occurs in mammals.
Keyphrases
- induced apoptosis
- cell cycle arrest
- gene expression
- signaling pathway
- oxidative stress
- endoplasmic reticulum stress
- type diabetes
- magnetic resonance
- stem cells
- cell death
- magnetic resonance imaging
- metabolic syndrome
- computed tomography
- adipose tissue
- mesenchymal stem cells
- transcription factor
- bone marrow
- pi k akt
- polycystic ovary syndrome