In Tyr mice, NAP corrected sex-specific spleen transcriptomic differences, including female antigen-processing and cellular-senescence effects.
In plain wordsIn mice, NAP corrected sex-specific differences in spleen gene activity.
- Peptide
- Davunetide
- Outcome
- Direction not reportedSex-specific spleen gene expression
- Study
mousen: not reported in source
Adnp p.Tyr718* mice- Outcome group
- Receptor activity and mechanism · Immune and inflammation
- Studied dose
- Dose not stated
Source sentences
RNA sequencing of spleens, representing a peripheral biomarker source, revealed Tyr-specific sex differences (e.g., cell cycle), accentuated in females (with significant effects on antigen processing and cellular senescence) and corrected by NAP.
2 context sentences(design, population, supporting numbers)
Mimicking humans, CRISPR (clustered regularly interspaced short palindromic repeats)-Cas9 editing produced mice carrying heterozygous Adnp p.Tyr718∗ (Tyr), a paralog of the most common ADNP syndrome mutation.
Phenotypic rescue was validated by treatment with the microtubule/autophagy-protective ADNP fragment NAPVSIPQ (NAP).