L(1)10Bb serves as a conservative determinant for soma-germline communications via cellular non-autonomous effects within the testicular stem cell niche.
Lei HeFeiteng SunYunhao WuZhiran LiYangbo FuQiuru HuangJiaxin LiZihan WangJiaying CaiChenrui FengXiaonan DengHan GuXuxin HeJun YuFei SunPublished in: Molecular and cellular endocrinology (2024)
The testicular stem cell niche is the central regulator of spermatogenesis in Drosophila melanogaster. However, the underlying regulatory mechanisms are unclear. This study demonstrated the crucial role of lethal (1) 10Bb [l(1)10Bb] in regulating the testicular stem cell niche. Dysfunction of l(1)10Bb in early-stage cyst cells led to male fertility disorders and compromised cyst stem cell maintenance. Moreover, the dysfunction of l(1)10Bb in early-stage cyst cells exerted non-autonomous effects on germline stem cell differentiation, independently of hub signals. Notably, our study highlights the rescue of testicular defects through ectopic expression of L(1)10Bb and the human homologous protein BUD31 homolog (BUD31). In addition, l(1)10Bb dysfunction in early-stage cyst cells downregulated the expression of spliceosome subunits in the Sm and the precursor RNA processing complexes. Collectively, our findings established l(1)10Bb as a pivotal factor in the modulation of Drosophila soma-germline communications within the testicular stem cell niche.
Keyphrases
- stem cells
- growth factor
- early stage
- induced apoptosis
- recombinant human
- germ cell
- cell cycle arrest
- oxidative stress
- dna repair
- poor prognosis
- drosophila melanogaster
- transcription factor
- sentinel lymph node
- endoplasmic reticulum stress
- dna damage
- cell proliferation
- young adults
- radiation therapy
- neoadjuvant chemotherapy
- locally advanced