Myosin VIIa Supports Spermatid/Organelle Transport and Cell Adhesion During Spermatogenesis in the Rat Testis.

Endocrinology

The Mary M. Wohlford Laboratory for Male Contraceptive Research, Center for Biomedical Research, Population Council, New York, New York.

Published: March 2019

The biology of transport of spermatids and spermatid adhesion across the seminiferous epithelium during the epithelial cycle remains largely unexplored. Nonetheless, studies have implicated the role of motor proteins in these cellular events. In this article, we report findings to unravel the role of myosin VIIa, an F-actin-based barbed (+)-end-directed motor protein, to support cellular transport and adhesion in the testis. Using RNA interference to knock down myosin VIIa in Sertoli cells cultured in vitro as a study model was shown to perturb the Sertoli cell tight junction permeability barrier, mediated through disorganization of actin- or microtubule (MT)-based cytoskeletons owing to disruptive changes on the spatiotemporal expression of F-actin or MT-regulatory proteins. Consistent with these in vitro findings, knockdown of myosin VIIa in the testis in vivo also induced disorganization of the actin- and MT-based cytoskeletons across the seminiferous epithelium, mediated by disruptive changes in the spatiotemporal expression of actin- and MT-based regulatory proteins. More important, the transport of spermatids and organelles across the epithelium, as well as cell adhesion, was grossly disrupted. For instance, step 19 spermatids failed to be transported to the adluminal compartment near the tubule lumen to undergo spermiation; in this manner, step 19 spermatids were persistently detected in stage IX and XII tubules, intermingling with step 9 and 12 spermatids, respectively. Also, phagosomes were detected near the tubule lumen in stage I to III tubules when they should have been degraded near the base of the seminiferous epithelium via the lysosomal pathway. In summary, myosin VIIa motor protein was crucial to support cellular transport and adhesion during spermatogenesis.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372944PMC
http://dx.doi.org/10.1210/en.2018-00855DOI Listing

Publication Analysis

Top Keywords

myosin viia
20
seminiferous epithelium
12
step spermatids
12
cell adhesion
8
adhesion spermatogenesis
8
transport spermatids
8
motor protein
8
support cellular
8
cellular transport
8
transport adhesion
8

Similar Publications

In the mammalian cochlea, sensory hair cells are crucial for the transduction of acoustic stimuli into electrical signals, which are then relayed to the central auditory pathway via spiral ganglion neuron (SGN) afferent dendrites. The SGN output is directly modulated by inhibitory cholinergic axodendritic synapses from the efferent fibers originating in the superior olivary complex. When the adult cochlea is subjected to noxious stimuli or aging, the efferent system undergoes major rewiring, such that it reestablishes direct axosomatic contacts with the inner hair cells (IHCs), which occur only transiently during prehearing stages of development.

View Article and Find Full Text PDF

Morphological mouse phenotyping plays a pivotal role in the translational setting and even more in the area of auditory research, where mouse is a central model organism due to the evolutionary genetic relationship and morpho-functional analogies with the human auditory system. However, some results obtained in murine models cannot be translated to humans due to the inadequate description of experimental conditions underlying poor reproducibility. We approach the characterization of the aging process of the mouse cochlea in animals up to 18 months of age belonging to two of the most used outbred (CD1) and inbred (C57BL/6N) strains.

View Article and Find Full Text PDF

Hearing loss (HL) is one of the most common health problems worldwide. Autosomal recessive non-syndromic sensorineural hearing loss (ARNSHL) represents a large portion of congenital hereditary HL. Our study was conducted on 13 patients from 13 unrelated families.

View Article and Find Full Text PDF
Article Synopsis
  • Cochlear hair cells are damaged by loud sounds, certain drugs, and aging, leading to irreversible hearing loss since they don't regenerate in mammals.
  • Research has shown that using a combination of three specific hair cell transcription factors can reprogram adjacent supporting cells into hair cell-like cells, particularly after inducing damage to the existing hair cells.
  • The reprogrammed cells displayed key characteristics of mature hair cells and remained responsive to reprogramming efforts for at least 6 weeks after damage, indicating potential for hearing restoration in chronically deaf individuals.
View Article and Find Full Text PDF

Genotype Characterization and MiRNA Expression Profiling in Usher Syndrome Cell Lines.

Int J Mol Sci

September 2024

Molecular Diagnostic Research Laboratory, Center for Sensory Neuroscience, Boys Town National Research Hospital, Omaha, NE 68010, USA.

Article Synopsis
  • Usher syndrome (USH) is a genetic disorder that causes hearing loss, vision loss due to retinitis pigmentosa, and balance issues, classified into three types without early detection biomarkers.
  • The study investigated the differences in microRNA (miRNA) expression in cell lines from USH patients versus healthy controls, using Epstein-Barr virus to transform lymphocytes for analysis.
  • Findings showed 92 miRNAs were differentially expressed in USH, with specific patterns tied to each type, and three crucial miRNAs associated with sensory development were notably downregulated, offering potential insights for identifying USH.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!