Stress-inducible phosphoprotein 1 (STIP1) is a critical stemness regulator in mouse embryonic stem cells and early mammalian development
Proteostasis, maintained by a network of molecular chaperones, plays a central role in cell biology, and has emerged as a critical mechanism underlying pluripotency and development. The stress-inducible phosphoprotein 1 (STIP1) is a co-chaperone essential for proteostasis. STIP1 knockout causes embryonic lethality in mice, but its precise function during embryogenesis remains poorly understood. Here, we investigate the role of STIP1 in early development using in silico and cell-based approaches. Single-cell RNA sequencing data reveals that Stip1 is co-expressed with pluripotency genes in mouse embryos, suggesting a role in stem cell maintenance. To test this, we generated mouse embryonic stem cells (mESCs) from genetically modified mice with altered Stip1/STIP1 expression. STIP1 depletion in mESCs decreases the expression of pluripotency markers, reduces proliferation, and induces apoptosis and genomic instability, whereas its overexpression enhances pluripotency markers expression, promotes proliferation, and confers protection against cellular stress. Moreover, proteins involved in cell cycle progression and DNA damage response are differentially regulated in mESCs, depending on STIP1 levels. Our findings highlight STIP1 as a pivotal regulator of the pluripotent phenotype, early embryogenesis, and cellular resilience, advancing our understanding of proteostasis in stem cell biology and organismal development, with potential implications for disease modeling and regenerative medicine.
Authors
- Tiago G. Santos (ORCID: https://orcid.org/0000-0001-6641-7413)
- Samuel Ribeiro Soares
- Rebeca Piatniczka Iglesia (ORCID: https://orcid.org/0000-0002-5852-2632)
- Camila Felix de Lima Fernandes (ORCID: https://orcid.org/0000-0001-5826-8905)
- João Pedro Alves de Araújo (ORCID: https://orcid.org/0000-0003-0822-2401)
- Marcelo Falchetti (ORCID: https://orcid.org/0000-0002-9438-680X)
- Maria Isabel Melo-Escobar (ORCID: https://orcid.org/0000-0003-3176-9181)
- Helder I. Nakaya (ORCID: https://orcid.org/0000-0001-5297-9108)
- Flávio H. Beraldo (ORCID: https://orcid.org/0000-0001-7638-2007)
- Mariana Brandão Prado
- Frederico Moraes Ferreira (ORCID: https://orcid.org/0000-0002-7403-9165)
- Vânia F. Prado (ORCID: https://orcid.org/0000-0003-4994-6393)
- Marco A. M. Prado (ORCID: https://orcid.org/0000-0002-3028-5778)
- Jacqueline Marcia Boccacino (ORCID: https://orcid.org/0000-0001-6813-5217)
- Marilene H. Lopes (ORCID: https://orcid.org/0000-0003-2496-0674)
- Maria Clara da Silva Souza (ORCID: https://orcid.org/0000-0002-4437-7147)
- Rachel E. Lackie
- Edroaldo Lummertz da Rocha (ORCID: https://orcid.org/0000-0003-0537-4223)
- Jenny Andrea Arévalo-Romero
- Bárbara Paranhos Coelho (ORCID: https://orcid.org/0000-0002-8475-0620)
Institutions
- Western University (CA)
- Universidade de São Paulo (BR)
- Hospital Israelita Albert Einstein (BR)
- AC Camargo Hospital (BR)
- Universidade Federal de Santa Catarina (BR)
- Institute of Biomedical Science (GB)
Publication Details
- Journal
- Communications Biology
- Published
- 2025-08-29
- DOI
- https://doi.org/10.1038/s42003-025-08763-9
- Primary Topic
- Genetics, Aging, and Longevity in Model Organisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Alzheimer's Association
- McGill University
- Alzheimer's Society
- Fundação de Amparo à Pesquisa do Estado de São Paulo
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Canada First Research Excellence Fund
- Alzheimer Society Research Program
- Canadian Institutes of Health Research