Data driven and cell specific determination of nuclei-associated actin structure.

F-actin LINC cytoskeleton machine learning mechanobiology nuclear envelope

Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
06 Apr 2023
Historique:
pubmed: 18 4 2023
medline: 18 4 2023
entrez: 17 4 2023
Statut: epublish

Résumé

Quantitative and volumetric assessment of filamentous actin fibers (F-actin) remains challenging due to their interconnected nature, leading researchers to utilize threshold based or qualitative measurement methods with poor reproducibility. Here we introduce a novel machine learning based methodology for accurate quantification and reconstruction of nuclei-associated F-actin. Utilizing a Convolutional Neural Network (CNN), we segment actin filaments and nuclei from 3D confocal microscopy images and then reconstruct each fiber by connecting intersecting contours on cross-sectional slices. This allowed measurement of the total number of actin filaments and individual actin filament length and volume in a reproducible fashion. Focusing on the role of F-actin in supporting nucleocytoskeletal connectivity, we quantified apical F-actin, basal F-actin, and nuclear architecture in mesenchymal stem cells (MSCs) following the disruption of the Linker of Nucleoskeleton and Cytoskeleton (LINC) Complexes. Disabling LINC in mesenchymal stem cells (MSCs) generated F-actin disorganization at the nuclear envelope characterized by shorter length and volume of actin fibers contributing a less elongated nuclear shape. Our findings not only present a new tool for mechanobiology but introduce a novel pipeline for developing realistic computational models based on quantitative measures of F-actin.

Identifiants

pubmed: 37066142
doi: 10.1101/2023.04.06.535937
pmc: PMC10104112
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIA NIH HHS
ID : R01 AG059923
Pays : United States
Organisme : NIH HHS
ID : S10 OD032354
Pays : United States

Déclaration de conflit d'intérêts

Competing interests The author(s) declare no competing interests financial or otherwise.

Auteurs

Nina Nikitina (N)

Boise State University.

Nurbanu Bursa (N)

University of Idaho.
Hacettepe University.

Matthew Goelzer (M)

Oral Roberts University.

Madison Goldfeldt (M)

Boise State University.

Chase Crandall (C)

Boise State University.

Sean Howard (S)

Boise State University.

Janet Rubin (J)

University of North Carolina at Chapel Hill.

Aykut Satici (A)

Boise State University.

Gunes Uzer (G)

Boise State University.

Classifications MeSH