Cellular shape reinforces niche to stem cell signaling in the small intestine

Author:

Pentinmikko Nalle1ORCID,Lozano Rodrigo23ORCID,Scharaw Sandra2,Andersson Simon1ORCID,Englund Johanna I.1ORCID,Castillo-Azofeifa David45ORCID,Gallagher Aaron4ORCID,Broberg Martin1,Song Ki-Young6,Sola Carvajal Agustín2ORCID,Speidel Alessondra T.6ORCID,Sundstrom Michael3,Allbritton Nancy7ORCID,Stevens Molly M.68ORCID,Klein Ophir D.4910ORCID,Teixeira Ana6,Katajisto Pekka1211ORCID

Affiliation:

1. Institute of Biotechnology, HiLIFE, University of Helsinki, Helsinki, Finland.

2. Department of Cell and Molecular Biology (CMB), Karolinska Institutet, Stockholm, Sweden.

3. Division of Rheumatology, Department of Medicine, Solna, Karolinska Institutet, and Karolinska University Hospital, Stockholm, Sweden.

4. Department of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, San Francisco, CA, USA.

5. Immunology Discovery, Genentech Inc., South San Francisco, CA, USA.

6. Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.

7. University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

8. Department of Materials and Department of Bioengineering, Imperial College London, UK.

9. Department of Pediatrics and Institute for Human Genetics, University of California, San Francisco, San Francisco, CA, USA.

10. Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

11. Molecular and Integrative Bioscience Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.

Abstract

Niche-derived factors regulate tissue stem cells, but apart from the mechanosensory pathways, the effect of niche geometry is not well understood. We used organoids and bioengineered tissue culture platforms to demonstrate that the conical shape of Lgr5 + small intestinal stem cells (ISCs) facilitate their self-renewal and function. Inhibition of non-muscle myosin II (NM II)–driven apical constriction altered ISC shape and reduced niche curvature and stem cell capacity. Niche curvature is decreased in aged mice, suggesting that suboptimal interactions between old ISCs and their niche develop with age. We show that activation of NM IIC or physical restriction to young topology improves in vitro regeneration by old epithelium. We propose that the increase in lateral surface area of ISCs induced by apical constriction promotes interactions between neighboring cells, and the curved topology of the intestinal niche has evolved to maximize signaling between ISCs and neighboring cells.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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