The temporal architecture of the seminiferous epithelial cycle revealed by spatial transcriptomics
Summary
bioRxiv. 2024 Nov 04:2024.10.28.620681. doi: 10.1101/2024.10.28.620681. Spermatogenesis features the seminiferous epithelial cycle, a periodic progression of germ-cell differentiation along the seminiferous tubules. Using seqFISH+ spatial transcriptomics, we profiled 2,653 genes in 867,062 mouse testis cells, revealing tubule-level transcriptional patterns that recapitulate the cycle and enable high-resolution temporal mapping of cells. Unlike other somatic cells, Sertoli cells exhibit a cy
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# The temporal architecture of the seminiferous epithelial cycle revealed by spatial transcriptomics
*Published: 2026 May 15*
bioRxiv. 2024 Nov 04:2024.10.28.620681. doi: 10.1101/2024.10.28.620681.
Spermatogenesis features the seminiferous epithelial cycle, a periodic
progression of germ-cell differentiation along the seminiferous tubules. Using
seqFISH+ spatial transcriptomics, we profiled 2,653 genes in 867,062 mouse
testis cells, revealing tubule-level transcriptional patterns that recapitulate
the cycle and enable high-resolution temporal mapping of cells. Unlike other
somatic cells, Sertoli cells exhibit a cyclic transcriptional profile
synchronized with spermatogenesis. This cyclicity persists in germ-cell-depleted
testes (busulfan and W/Wv), although with gene-specific dephasing and reduced
amplitude, supporting an intrinsic Sertoli cyclic program. We identify retinoic
acid (RA) as a permissive signal: germ-cell-depleted Sertoli cells cycle RA
enzymes, while inhibiting RA synthesis via WIN 18,446 arrests them mid-cycle.
Ligand-receptor analysis reveals bidirectional germ-Sertoli signaling. Notably,
Wnt inhibition with LGK974 partially recapitulates germ-cell-depletion dephasing
and amplitude changes. These findings support an integrative model where an
intrinsic Sertoli program maintains baseline periodicity, while germ-cell
signals refine the cycle to coordinate spermatogenesis.
DOI: 10.1016/j.cell.2026.04.036