Abstract
Patient-derived organoids and cellular spheroids recapitulate tissue physiology with remarkable fidelity. We investigated how engagement with a reconstituted basement membrane in three dimensions (3D) supports the polarized, stress resilient tissue phenotype of mammary epithelial spheroids. Cells interacting with reconstituted basement membrane in 3D had reduced levels of total and actin-associated filamin and decreased cortical actin tension that increased plasma membrane protrusions to promote negative plasma membrane curvature and plasma membrane protein associations linked to protein secretion. By contrast, cells engaging a reconstituted basement membrane in 2D had high cortical actin tension that forced filamin unfolding and endoplasmic reticulum (ER) associations. Enhanced filamin-ER interactions increased levels of PKR-like ER kinase effectors and ER-plasma membrane contact sites that compromised calcium homeostasis and diminished cell viability. Consequently, cells with decreased cortical actin tension had reduced ER stress and survived better. Consistently, cortical actin tension in cellular spheroids regulated polarized basement membrane membrane deposition and sensitivity to exogenous stress. The findings implicate cortical actin tension-mediated filamin unfolding in ER function and underscore the importance of tissue mechanics in organoid homeostasis.
| Original language | English |
|---|---|
| Article number | e109205 |
| Journal | EMBO Journal |
| Volume | 41 |
| Issue number | 17 |
| DOIs | |
| State | Published - Sep 1 2022 |
Bibliographical note
Publisher Copyright:© 2022 The Authors.
Funding
We wish to acknowledge the experimental contributions of Drs. Christian Franz and Jordi Alcarez for their pilot studies that provided essential proof of concept upon which the rationale for the expanded studies summarized in the current manuscript were based. We would also like to acknowledge Dr. Johnathon N. Lakins for his technical assistance and Delaine Larsen and SoYeon Kim from the Nikon Imaging Center at UCSF for their support with image processing. This work was supported by the following grants: US National Institutes of Health NCI grants R35 CA242447-01A1; R01CA222508-01; U01 CA202241 and U01 CA250044-01A1; and BCRF A132292 (V.M.W.); P01 GM121203 (N.V.); Canadian Institutes of Health Research Postdoctoral Fellowship (F.B.K.); National Science Foundation Graduate Research Fellowship (G.O. and A.F.L); U01 grant CA202241 (C.S.); NIH R01GM1341 (S.D); NCI1U01CA202123 (Y.L.H and M.G.); NIH/NIGMS DP2OD022552 (H.H.H. and A.P.W.); American Association for Cancer Research Basic Cancer Research Fellowship (J.J.N.); NIH R35 GM141832 (W.G.); NIH CA227550 and CA193417 (R.R. and R.W.T); Banting Postdoctoral Fellowship from the Government of Canada (A.M.L.). D.H. and N.V. acknowledge the use of the Titan Krios, Tecnai Spirit T12 and auxiliary equipment at the cryo-EM unit of the Sanford Burnham Prebys Medical Discovery Institute, which was created in part with the support of US National Institutes of Health Grant S10-OD012372 (D.H.) and Pew Charitable Trust 864K625 innovation award funds (D.H.). We wish to acknowledge the experimental contributions of Drs. Christian Franz and Jordi Alcarez for their pilot studies that provided essential proof of concept upon which the rationale for the expanded studies summarized in the current manuscript were based. We would also like to acknowledge Dr. Johnathon N. Lakins for his technical assistance and Delaine Larsen and SoYeon Kim from the Nikon Imaging Center at UCSF for their support with image processing. This work was supported by the following grants: US National Institutes of Health NCI grants R35 CA242447‐01A1; R01CA222508‐01; U01 CA202241 and U01 CA250044‐01A1; and BCRF A132292 (V.M.W.); P01 GM121203 (N.V.); Canadian Institutes of Health Research Postdoctoral Fellowship (F.B.K.); National Science Foundation Graduate Research Fellowship (G.O. and A.F.L); U01 grant CA202241 (C.S.); NIH R01GM1341 (S.D); NCI1U01CA202123 (Y.L.H and M.G.); NIH/NIGMS DP2OD022552 (H.H.H. and A.P.W.); American Association for Cancer Research Basic Cancer Research Fellowship (J.J.N.); NIH R35 GM141832 (W.G.); NIH CA227550 and CA193417 (R.R. and R.W.T); Banting Postdoctoral Fellowship from the Government of Canada (A.M.L.). D.H. and N.V. acknowledge the use of the Titan Krios, Tecnai Spirit T12 and auxiliary equipment at the cryo‐EM unit of the Sanford Burnham Prebys Medical Discovery Institute, which was created in part with the support of US National Institutes of Health Grant S10‐OD012372 (D.H.) and Pew Charitable Trust 864K625 innovation award funds (D.H.).
| Funders | Funder number |
|---|---|
| National Science Foundation Arctic Social Science Program | |
| Canada Excellence Research Chairs, Government of Canada | |
| Nikon Imaging Center at UCSF | |
| Canadian Institutes of Health Research | |
| Pew Charitable Trusts | |
| National Childhood Cancer Registry – National Cancer Institute | U01CA202241, R35CA242447, U01CA250044, U01CA227550, U54CA193417, U01CA202123 |
| National Institutes of Health (NIH) | R01CA222508‐01, BCRF A132292, R01GM1341 |
| American Association for Cancer Research | R35 GM141832 |
| National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical Sciences | R35GM141832, P01GM121203, DP2OD022552 |
| NIH Office of the Director | S10OD012372 |
Keywords
- actin tension
- endoplasmic reticulum
- extracellular matrix
- membrane contact sites
- spheroids
ASJC Scopus subject areas
- General Neuroscience
- Molecular Biology
- General Biochemistry, Genetics and Molecular Biology
- General Immunology and Microbiology
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