The architecture of cell differentiation in choanoflagellates and sponge choanocytes.

Although collar cells are conserved across animals and their closest relatives, the choanoflagellates, little is known about their ancestry, their subcellular architecture, or how they differentiate. The choanoflagellate Salpingoeca rosetta expresses genes necessary for animal development and can al...

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Main Authors: Davis Laundon, Ben T Larson, Kent McDonald, Nicole King, Pawel Burkhardt
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-04-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.3000226
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spelling doaj-223e999d7e694303a1d3a23d7468182c2021-07-02T16:28:56ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852019-04-01174e300022610.1371/journal.pbio.3000226The architecture of cell differentiation in choanoflagellates and sponge choanocytes.Davis LaundonBen T LarsonKent McDonaldNicole KingPawel BurkhardtAlthough collar cells are conserved across animals and their closest relatives, the choanoflagellates, little is known about their ancestry, their subcellular architecture, or how they differentiate. The choanoflagellate Salpingoeca rosetta expresses genes necessary for animal development and can alternate between unicellular and multicellular states, making it a powerful model for investigating the origin of animal multicellularity and mechanisms underlying cell differentiation. To compare the subcellular architecture of solitary collar cells in S. rosetta with that of multicellular 'rosette' colonies and collar cells in sponges, we reconstructed entire cells in 3D through transmission electron microscopy on serial ultrathin sections. Structural analysis of our 3D reconstructions revealed important differences between single and colonial choanoflagellate cells, with colonial cells exhibiting a more amoeboid morphology consistent with higher levels of macropinocytotic activity. Comparison of multiple reconstructed rosette colonies highlighted the variable nature of cell sizes, cell-cell contact networks, and colony arrangement. Importantly, we uncovered the presence of elongated cells in some rosette colonies that likely represent a distinct and differentiated cell type, pointing toward spatial cell differentiation. Intercellular bridges within choanoflagellate colonies displayed a variety of morphologies and connected some but not all neighbouring cells. Reconstruction of sponge choanocytes revealed ultrastructural commonalities but also differences in major organelle composition in comparison to choanoflagellates. Together, our comparative reconstructions uncover the architecture of cell differentiation in choanoflagellates and sponge choanocytes and constitute an important step in reconstructing the cell biology of the last common ancestor of animals.https://doi.org/10.1371/journal.pbio.3000226
collection DOAJ
language English
format Article
sources DOAJ
author Davis Laundon
Ben T Larson
Kent McDonald
Nicole King
Pawel Burkhardt
spellingShingle Davis Laundon
Ben T Larson
Kent McDonald
Nicole King
Pawel Burkhardt
The architecture of cell differentiation in choanoflagellates and sponge choanocytes.
PLoS Biology
author_facet Davis Laundon
Ben T Larson
Kent McDonald
Nicole King
Pawel Burkhardt
author_sort Davis Laundon
title The architecture of cell differentiation in choanoflagellates and sponge choanocytes.
title_short The architecture of cell differentiation in choanoflagellates and sponge choanocytes.
title_full The architecture of cell differentiation in choanoflagellates and sponge choanocytes.
title_fullStr The architecture of cell differentiation in choanoflagellates and sponge choanocytes.
title_full_unstemmed The architecture of cell differentiation in choanoflagellates and sponge choanocytes.
title_sort architecture of cell differentiation in choanoflagellates and sponge choanocytes.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2019-04-01
description Although collar cells are conserved across animals and their closest relatives, the choanoflagellates, little is known about their ancestry, their subcellular architecture, or how they differentiate. The choanoflagellate Salpingoeca rosetta expresses genes necessary for animal development and can alternate between unicellular and multicellular states, making it a powerful model for investigating the origin of animal multicellularity and mechanisms underlying cell differentiation. To compare the subcellular architecture of solitary collar cells in S. rosetta with that of multicellular 'rosette' colonies and collar cells in sponges, we reconstructed entire cells in 3D through transmission electron microscopy on serial ultrathin sections. Structural analysis of our 3D reconstructions revealed important differences between single and colonial choanoflagellate cells, with colonial cells exhibiting a more amoeboid morphology consistent with higher levels of macropinocytotic activity. Comparison of multiple reconstructed rosette colonies highlighted the variable nature of cell sizes, cell-cell contact networks, and colony arrangement. Importantly, we uncovered the presence of elongated cells in some rosette colonies that likely represent a distinct and differentiated cell type, pointing toward spatial cell differentiation. Intercellular bridges within choanoflagellate colonies displayed a variety of morphologies and connected some but not all neighbouring cells. Reconstruction of sponge choanocytes revealed ultrastructural commonalities but also differences in major organelle composition in comparison to choanoflagellates. Together, our comparative reconstructions uncover the architecture of cell differentiation in choanoflagellates and sponge choanocytes and constitute an important step in reconstructing the cell biology of the last common ancestor of animals.
url https://doi.org/10.1371/journal.pbio.3000226
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