A joint alignment and reconstruction algorithm for electron tomography to visualize in-depth cell-to-cell interactions.

Electron microscopy Electron tomography Fiducial-less alignment Inverse problem Joint alignment and reconstruction algorithm Primal-dual iterative reconstruction

Journal

Histochemistry and cell biology
ISSN: 1432-119X
Titre abrégé: Histochem Cell Biol
Pays: Germany
ID NLM: 9506663

Informations de publication

Date de publication:
Jun 2022
Historique:
accepted: 24 02 2022
pubmed: 24 3 2022
medline: 25 5 2022
entrez: 23 3 2022
Statut: ppublish

Résumé

Electron tomography allows one to obtain 3D reconstructions visualizing a tissue's ultrastructure from a series of 2D projection images. An inherent problem with this imaging technique is that its projection images contain unwanted shifts, which must be corrected for to achieve reliable reconstructions. Commonly, the projection images are aligned with each other by means of fiducial markers prior to the reconstruction procedure. In this work, we propose a joint alignment and reconstruction algorithm that iteratively solves for both the unknown reconstruction and the unintentional shift and does not require any fiducial markers. We evaluate the approach first on synthetic phantom data where the focus is not only on the reconstruction quality but more importantly on the shift correction. Subsequently, we apply the algorithm to healthy C57BL/6J mice and then compare it with non-obese diabetic (NOD) mice, with the aim of visualizing the attack of immune cells on pancreatic beta cells within type 1 diabetic mice at a more profound level through 3D analysis. We empirically demonstrate that the proposed algorithm is able to compute the shift with a remaining error at only the sub-pixel level and yields high-quality reconstructions for the limited-angle inverse problem. By decreasing labour and material costs, the algorithm facilitates further research directed towards investigating the immune system's attacks in pancreata of NOD mice for numerous samples at different stages of type 1 diabetes.

Identifiants

pubmed: 35318489
doi: 10.1007/s00418-022-02095-z
pii: 10.1007/s00418-022-02095-z
pmc: PMC9124659
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

685-696

Subventions

Organisme : Juvenile Diabetes Research Foundation United States of America
ID : 2021-1043-S-B
Organisme : BioTechMed
ID : MIDAS

Informations de copyright

© 2022. The Author(s).

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Auteurs

Lea Bogensperger (L)

Institute of Computer Graphics and Vision, Graz University of Technology, Graz, Austria.

Erich Kobler (E)

Institute of Computer Graphics, University of Linz, Linz, Austria.

Dominique Pernitsch (D)

Core Facility Ultrastructure Analysis, Neue Stiftingtalstraße 6/II, 8010, Graz, Austria.

Petra Kotzbeck (P)

COREMED, Cooperative Centre for Regenerative Medicine, Joanneum Research Forschungsgesellschaft mbH, Graz, Austria.
The Research Unit for Tissue Regeneration, Repair and Reconstruction, c/o Division of Plastic, Aesthetic and Reconstructive Surgery, Department of Surgery, Medical University of Graz, Graz, Austria.

Thomas R Pieber (TR)

Division of Endocrinology and Diabetology, Medical University of Graz, Graz, Austria.
The Center for Biomarker Research in Medicine GmbH, Graz, Austria.

Thomas Pock (T)

Institute of Computer Graphics and Vision, Graz University of Technology, Graz, Austria. pock@icg.tugraz.at.

Dagmar Kolb (D)

Core Facility Ultrastructure Analysis, Neue Stiftingtalstraße 6/II, 8010, Graz, Austria. dagmar.kolb@medunigraz.at.
Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Division of Cell Biology, Histology and Embryology, Medical University of Graz, Neue Stiftingtalstraße 6/II, 8010, Graz, Austria. dagmar.kolb@medunigraz.at.

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Classifications MeSH