4.6 Article

Functional Specificity of the Members of the Sos Family of Ras-GEF Activators: Novel Role of Sos2 in Control of Epidermal Stem Cell Homeostasis

Journal

CANCERS
Volume 13, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13092152

Keywords

Sos1; Sos2; GEF; KO; Ras signaling; keratinocytes; skin homeostasis

Categories

Funding

  1. ISCIII-MCUI [FIS PI19/00934]
  2. JCyL [SA264P18-UIC 076]
  3. Areces Foundation [CIVP19A5942]
  4. Solorzano-Barruso Foundation [FS/32-2020]
  5. ISCIII-CIBERONC [CB16/12/00352]
  6. FEDER funds
  7. European Regional Development Fund (FEDER) grants from Science and Innovation [SAF2015-66015-R, PID2019-110758RB-I00]
  8. Instituto de Salud Carlos III (CIBERONC) [CB16/12/00228]
  9. la Caixa Banking Foundation [HR20-00164]
  10. Castilla-Leon autonomous government [CSI252P18, CSI145P20, CLC-2017-01]
  11. Spanish Ministry of Science and Innovation (MSI) [RTI2018-096481-B-100]
  12. Spanish Association against Cancer [GC16173472GARC]
  13. Programa de Apoyo a Planes Estrategicos de Investigacion de Estructuras de Investigacion de Excelencia of the Castilla-Leon autonomous government [CLC-2017-01]
  14. Spanish Ministry of Universities [FPU13/02923, FPU17/03912]

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Sos1 and Sos2 have overlapping roles in proliferation and survival in skin cells, with Sos1 focusing on the ERK pathway and Sos2 controlling the PI3K pathway. Sos2 plays a crucial role in regulating the population of epidermal stem cells.
Simple Summary The Sos Ras-GEFs are known to participate in a wide range of skin-related diseases including cutaneous cancers, cardio-facio-cutaneous syndromes, or hirsutism. However, the specific functional roles played by the Sos1 and/or Sos2 family members in specific skin compartments remain largely unknown. This report aimed at precisely characterizing the specific functions played by Sos1 and/or Sos2 in keratinocytes, an essential cellular component of the skin. Our data show that Sos1 and Sos2 make overlapping contributions to both keratinocyte proliferation and survival. However, Sos1 seems to have a preferential involvement in regulating the ERK axis, whereas Sos2 seems to control the signaling output from the PI3K axis. We also uncovered an essential role of Sos2 in the control of the population of epidermal stem cells. Prior reports showed the critical requirement of Sos1 for epithelial carcinogenesis, but the specific functionalities of the homologous Sos1 and Sos2 GEFs in skin homeostasis and tumorigenesis remain unclear. Here, we characterize specific mechanistic roles played by Sos1 or Sos2 in primary mouse keratinocytes (a prevalent skin cell lineage) under different experimental conditions. Functional analyses of actively growing primary keratinocytes of relevant genotypes-WT, Sos1-KO, Sos2-KO, and Sos1/2-DKO-revealed a prevalent role of Sos1 regarding transcriptional regulation and control of RAS activation and mechanistic overlapping of Sos1 and Sos2 regarding cell proliferation and survival, with dominant contribution of Sos1 to the RAS-ERK axis and Sos2 to the RAS-PI3K/AKT axis. Sos1/2-DKO keratinocytes could not grow under 3D culture conditions, but single Sos1-KO and Sos2-KO keratinocytes were able to form pseudoepidermis structures that showed disorganized layer structure, reduced proliferation, and increased apoptosis in comparison with WT 3D cultures. Remarkably, analysis of the skin of both newborn and adult Sos2-KO mice uncovered a significant reduction of the population of stem cells located in hair follicles. These data confirm that Sos1 and Sos2 play specific, cell-autonomous functions in primary keratinocytes and reveal a novel, essential role of Sos2 in control of epidermal stem cell homeostasis.

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