The Role of Plzf in Spermatogonial Stem Cell Maintenance and Differentiation: Mapping the Transcriptional Dynamics and Key Interactions
Spermatogonial stem cells (SSCs) sustain and modulate spermatogenesis through intricate signaling pathways and transcription factors. Promyelocytic leukemia zinc-finger (<i>Plzf</i>, also known as <i>Zbtb16</i>) has been identified as a critical transcription factor influenci...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2024-11-01
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| Series: | Cells |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4409/13/23/1930 |
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| Summary: | Spermatogonial stem cells (SSCs) sustain and modulate spermatogenesis through intricate signaling pathways and transcription factors. Promyelocytic leukemia zinc-finger (<i>Plzf</i>, also known as <i>Zbtb16</i>) has been identified as a critical transcription factor influencing various signaling and differentiation pathways. <i>Plzf</i> plays a pivotal role in regulating the differentiation properties of SSCs and is essential for the proper maintenance of spermatogenesis. However, the transcription patterns of <i>Plzf</i> along the seminiferous tubules and its interaction network with adjacent partners still need to be fully elucidated. This study employed immunostaining techniques coupled with Fluidigm quantitative real-time polymerase chain reaction (Fluidigm qPCR) to quantify <i>Plzf</i> expression in undifferentiated and differentiated spermatogonia. Furthermore, we utilized bioinformatics analyses to identify <i>Plzf</i> partners and their associations with other regulatory factors. Immunohistostaining (IMH) revealed a high expression of <i>Plzf</i> in cells near the basal membrane of seminiferous tubules and a lower expression in the middle regions in vivo. Immunocytochemistry (ICC) demonstrated that undifferentiated spermatogonia exhibited significant <i>Plzf</i> positivity, whereas differentiated spermatogonia showed reduced <i>Plzf</i> expression in vitro. Fluidigm qPCR confirmed a significant differential expression of <i>Plzf</i> between undifferentiated and differentiated spermatogonia. In silico differential expression analysis between undifferentiated spermatogonia and spermatids indicated that <i>Plzf</i> is closely associated with <i>Mycn</i>, <i>Lin28a</i>, <i>Kras</i>, <i>Ccnd1</i>, and <i>Jak1</i>, highlighting the importance of these partnerships during spermatogenesis. Our findings suggest that the network of <i>Plzf</i>-related partners and their associated proteins involves differentiation, localization, apoptosis, and signal transduction. This comprehensive approach advances our understanding of <i>Plzf</i> transcription patterns and sheds light on its interactions with other cellular factors, revealing previously obscure pathways and interactions. These insights could lead to more effective diagnostic strategies for reproductive system-related diseases and inform the development of improved therapeutic and clinical applications. |
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| ISSN: | 2073-4409 |