TY - GEN
T1 - Joint segmentation and pairing of nuclei and Golgi in 3D microscopy images
AU - Narotamo, Hemaxi
AU - Ouarne, Marie
AU - Franco, Claudio Areias
AU - Silveira, Margarida
N1 - Funding Information:
FCT Project UIDB/50009/2020. M.O was supported by EU Horizon 2020 Marie Sklodowska-Curie fellowship (842498).
Publisher Copyright:
© 2021 IEEE.
PY - 2021
Y1 - 2021
N2 - Blood vessels provide oxygen and nutrients to all tissues in the human body, and their incorrect organisation or dysfunction contributes to several diseases. Correct organisation of blood vessels is achieved through vascular patterning, a process that relies on endothelial cell polarization and migration against the blood flow direction. Unravelling the mechanisms governing endothelial cell polarity is essential to study the process of vascular patterning. Cell polarity is defined by a vector that goes from the nucleus centroid to the corresponding Golgi complex centroid, here defined as axial polarity. Currently, axial polarity is calculated manually, which is time-consuming and subjective. In this work, we used a deep learning approach to segment nuclei and Golgi in 3D fluorescence microscopy images of mouse retinas, and to assign nucleus-Golgi pairs. This approach predicts nuclei and Golgi segmentation masks but also a third mask corresponding to joint nuclei and Golgi segmentations. The joint segmentation mask is used to perform nucleus-Golgi pairing. We demonstrate that our deep learning approach using three masks successfully identifies nucleus-Golgi pairs, outperforming a pairing method based on a cost matrix. Our results pave the way for automated computation of axial polarity in 3D tissues and in vivo.
AB - Blood vessels provide oxygen and nutrients to all tissues in the human body, and their incorrect organisation or dysfunction contributes to several diseases. Correct organisation of blood vessels is achieved through vascular patterning, a process that relies on endothelial cell polarization and migration against the blood flow direction. Unravelling the mechanisms governing endothelial cell polarity is essential to study the process of vascular patterning. Cell polarity is defined by a vector that goes from the nucleus centroid to the corresponding Golgi complex centroid, here defined as axial polarity. Currently, axial polarity is calculated manually, which is time-consuming and subjective. In this work, we used a deep learning approach to segment nuclei and Golgi in 3D fluorescence microscopy images of mouse retinas, and to assign nucleus-Golgi pairs. This approach predicts nuclei and Golgi segmentation masks but also a third mask corresponding to joint nuclei and Golgi segmentations. The joint segmentation mask is used to perform nucleus-Golgi pairing. We demonstrate that our deep learning approach using three masks successfully identifies nucleus-Golgi pairs, outperforming a pairing method based on a cost matrix. Our results pave the way for automated computation of axial polarity in 3D tissues and in vivo.
UR - http://www.scopus.com/inward/record.url?scp=85122505168&partnerID=8YFLogxK
U2 - 10.1109/EMBC46164.2021.9630362
DO - 10.1109/EMBC46164.2021.9630362
M3 - Conference contribution
C2 - 34891879
AN - SCOPUS:85122505168
T3 - Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBS
SP - 3017
EP - 3020
BT - 43rd Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2021
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 43rd Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2021
Y2 - 1 November 2021 through 5 November 2021
ER -