Spatial models of pattern formation during phagocytosis.

Phagocytosis, the biological process in which cells ingest large particles such as bacteria, is a key component of the innate immune response. Fcγ receptor (FcγR)-mediated phagocytosis is initiated when these receptors are activated after binding immunoglobulin G (IgG). Receptor activation initiates...

Full description

Bibliographic Details
Main Authors: John Cody Herron, Shiqiong Hu, Bei Liu, Takashi Watanabe, Klaus M Hahn, Timothy C Elston
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-10-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1010092
_version_ 1797831722259185664
author John Cody Herron
Shiqiong Hu
Bei Liu
Takashi Watanabe
Klaus M Hahn
Timothy C Elston
author_facet John Cody Herron
Shiqiong Hu
Bei Liu
Takashi Watanabe
Klaus M Hahn
Timothy C Elston
author_sort John Cody Herron
collection DOAJ
description Phagocytosis, the biological process in which cells ingest large particles such as bacteria, is a key component of the innate immune response. Fcγ receptor (FcγR)-mediated phagocytosis is initiated when these receptors are activated after binding immunoglobulin G (IgG). Receptor activation initiates a signaling cascade that leads to the formation of the phagocytic cup and culminates with ingestion of the foreign particle. In the experimental system termed "frustrated phagocytosis", cells attempt to internalize micropatterned disks of IgG. Cells that engage in frustrated phagocytosis form "rosettes" of actin-enriched structures called podosomes around the IgG disk. The mechanism that generates the rosette pattern is unknown. We present data that supports the involvement of Cdc42, a member of the Rho family of GTPases, in pattern formation. Cdc42 acts downstream of receptor activation, upstream of actin polymerization, and is known to play a role in polarity establishment. Reaction-diffusion models for GTPase spatiotemporal dynamics exist. We demonstrate how the addition of negative feedback and minor changes to these models can generate the experimentally observed rosette pattern of podosomes. We show that this pattern formation can occur through two general mechanisms. In the first mechanism, an intermediate species forms a ring of high activity around the IgG disk, which then promotes rosette organization. The second mechanism does not require initial ring formation but relies on spatial gradients of intermediate chemical species that are selectively activated over the IgG patch. Finally, we analyze the models to suggest experiments to test their validity.
first_indexed 2024-04-09T13:56:14Z
format Article
id doaj.art-f7ee124af7934947bb6a3ae023d5663b
institution Directory Open Access Journal
issn 1553-734X
1553-7358
language English
last_indexed 2024-04-09T13:56:14Z
publishDate 2022-10-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Computational Biology
spelling doaj.art-f7ee124af7934947bb6a3ae023d5663b2023-05-08T05:31:19ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582022-10-011810e101009210.1371/journal.pcbi.1010092Spatial models of pattern formation during phagocytosis.John Cody HerronShiqiong HuBei LiuTakashi WatanabeKlaus M HahnTimothy C ElstonPhagocytosis, the biological process in which cells ingest large particles such as bacteria, is a key component of the innate immune response. Fcγ receptor (FcγR)-mediated phagocytosis is initiated when these receptors are activated after binding immunoglobulin G (IgG). Receptor activation initiates a signaling cascade that leads to the formation of the phagocytic cup and culminates with ingestion of the foreign particle. In the experimental system termed "frustrated phagocytosis", cells attempt to internalize micropatterned disks of IgG. Cells that engage in frustrated phagocytosis form "rosettes" of actin-enriched structures called podosomes around the IgG disk. The mechanism that generates the rosette pattern is unknown. We present data that supports the involvement of Cdc42, a member of the Rho family of GTPases, in pattern formation. Cdc42 acts downstream of receptor activation, upstream of actin polymerization, and is known to play a role in polarity establishment. Reaction-diffusion models for GTPase spatiotemporal dynamics exist. We demonstrate how the addition of negative feedback and minor changes to these models can generate the experimentally observed rosette pattern of podosomes. We show that this pattern formation can occur through two general mechanisms. In the first mechanism, an intermediate species forms a ring of high activity around the IgG disk, which then promotes rosette organization. The second mechanism does not require initial ring formation but relies on spatial gradients of intermediate chemical species that are selectively activated over the IgG patch. Finally, we analyze the models to suggest experiments to test their validity.https://doi.org/10.1371/journal.pcbi.1010092
spellingShingle John Cody Herron
Shiqiong Hu
Bei Liu
Takashi Watanabe
Klaus M Hahn
Timothy C Elston
Spatial models of pattern formation during phagocytosis.
PLoS Computational Biology
title Spatial models of pattern formation during phagocytosis.
title_full Spatial models of pattern formation during phagocytosis.
title_fullStr Spatial models of pattern formation during phagocytosis.
title_full_unstemmed Spatial models of pattern formation during phagocytosis.
title_short Spatial models of pattern formation during phagocytosis.
title_sort spatial models of pattern formation during phagocytosis
url https://doi.org/10.1371/journal.pcbi.1010092
work_keys_str_mv AT johncodyherron spatialmodelsofpatternformationduringphagocytosis
AT shiqionghu spatialmodelsofpatternformationduringphagocytosis
AT beiliu spatialmodelsofpatternformationduringphagocytosis
AT takashiwatanabe spatialmodelsofpatternformationduringphagocytosis
AT klausmhahn spatialmodelsofpatternformationduringphagocytosis
AT timothycelston spatialmodelsofpatternformationduringphagocytosis