Loading…
The Role of Cell Membrane Information Reception, Processing, and Communication in the Structure and Function of Multicellular Tissue
Investigations of information dynamics in eukaryotic cells focus almost exclusively on heritable information in the genome. Gene networks are modeled as "central processors" that receive, analyze, and respond to intracellular and extracellular signals with the nucleus described as a cell...
Saved in:
Published in: | International journal of molecular sciences 2019-07, Vol.20 (15), p.3609 |
---|---|
Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c478t-d7514717fc5e3fc769536d6f6a9f61fe3338a147a9a408dab98f25ff807d70a53 |
---|---|
cites | cdi_FETCH-LOGICAL-c478t-d7514717fc5e3fc769536d6f6a9f61fe3338a147a9a408dab98f25ff807d70a53 |
container_end_page | |
container_issue | 15 |
container_start_page | 3609 |
container_title | International journal of molecular sciences |
container_volume | 20 |
creator | Gatenby, Robert A |
description | Investigations of information dynamics in eukaryotic cells focus almost exclusively on heritable information in the genome. Gene networks are modeled as "central processors" that receive, analyze, and respond to intracellular and extracellular signals with the nucleus described as a cell's control center. Here, we present a model in which cellular information is a distributed system that includes non-genomic information processing in the cell membrane that may quantitatively exceed that of the genome. Within this model, the nucleus largely acts a source of macromolecules and processes information needed to synchronize their production with temporal variations in demand. However, the nucleus cannot produce microsecond responses to acute, life-threatening perturbations and cannot spatially resolve incoming signals or direct macromolecules to the cellular regions where they are needed. In contrast, the cell membrane, as the interface with its environment, can rapidly detect, process, and respond to external threats and opportunities through the large amounts of potential information encoded within the transmembrane ion gradient. Our model proposes environmental information is detected by specialized protein gates within ion-specific transmembrane channels. When the gate receives a specific environmental signal, the ion channel opens and the received information is communicated into the cell via flow of a specific ion species (i.e., K
, Na
, Cl
, Ca
, Mg
) along electrochemical gradients. The fluctuation of an ion concentration within the cytoplasm adjacent to the membrane channel can elicit an immediate, local response by altering the location and function of peripheral membrane proteins. Signals that affect a larger surface area of the cell membrane and/or persist over a prolonged time period will produce similarly cytoplasmic changes on larger spatial and time scales. We propose that as the amplitude, spatial extent, and duration of changes in cytoplasmic ion concentrations increase, the information can be communicated to the nucleus and other intracellular structure through ion flows along elements of the cytoskeleton to the centrosome (via microtubules) or proteins in the nuclear membrane (via microfilaments). These dynamics add spatial and temporal context to the more well-recognized information communication from the cell membrane to the nucleus following ligand binding to membrane receptors. Here, the signal is transmitted and amplified through transdu |
doi_str_mv | 10.3390/ijms20153609 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_1a5a3bae0d5f4fa4855f3f308809f1b1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_1a5a3bae0d5f4fa4855f3f308809f1b1</doaj_id><sourcerecordid>2265766946</sourcerecordid><originalsourceid>FETCH-LOGICAL-c478t-d7514717fc5e3fc769536d6f6a9f61fe3338a147a9a408dab98f25ff807d70a53</originalsourceid><addsrcrecordid>eNpdks1vEzEQxVcIREvhxhlZ4sIhAX-svbsXpCqiEKkVqISzNfGOU0e7drDXSNz5w3GSUqWcPPL89ObN01TVa0bfC9HRD247Jk6ZFIp2T6pzVnM-p1Q1T0_qs-pFSltKueCye16dCSbqumnFefVndYfkNgxIgiULHAZyg-M6gkey9DbEESYXPLlFg7t9NSPfYjCYkvObGQHfk0UYx-ydOYLOk6kofp9iNlOOeECusjeHbplxk4fJmTIoDxDJyqWU8WX1zMKQ8NX9e1H9uPq0WnyZX3_9vFxcXs9NMTvN-0ayumGNNRKFNY3qytK9sgo6q5hFIUQLhYAOatr2sO5ay6W1LW36hoIUF9XyqNsH2OpddCPE3zqA04ePEDcaYnE3oGYgQawBaS9tbaFupbTCCtq2tLNszYrWx6PWLq9H7A36KcLwSPRxx7s7vQm_tFKdEoIXgXf3AjH8zJgmPbq0D6ZkH3LSnCvZFLhWBX37H7oNOfoSleZlaSWpVHtHsyNlYkgpon0ww6jen4o-PZWCvzld4AH-dxviL6XKu6g</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2333650561</pqid></control><display><type>article</type><title>The Role of Cell Membrane Information Reception, Processing, and Communication in the Structure and Function of Multicellular Tissue</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Gatenby, Robert A</creator><creatorcontrib>Gatenby, Robert A</creatorcontrib><description>Investigations of information dynamics in eukaryotic cells focus almost exclusively on heritable information in the genome. Gene networks are modeled as "central processors" that receive, analyze, and respond to intracellular and extracellular signals with the nucleus described as a cell's control center. Here, we present a model in which cellular information is a distributed system that includes non-genomic information processing in the cell membrane that may quantitatively exceed that of the genome. Within this model, the nucleus largely acts a source of macromolecules and processes information needed to synchronize their production with temporal variations in demand. However, the nucleus cannot produce microsecond responses to acute, life-threatening perturbations and cannot spatially resolve incoming signals or direct macromolecules to the cellular regions where they are needed. In contrast, the cell membrane, as the interface with its environment, can rapidly detect, process, and respond to external threats and opportunities through the large amounts of potential information encoded within the transmembrane ion gradient. Our model proposes environmental information is detected by specialized protein gates within ion-specific transmembrane channels. When the gate receives a specific environmental signal, the ion channel opens and the received information is communicated into the cell via flow of a specific ion species (i.e., K
, Na
, Cl
, Ca
, Mg
) along electrochemical gradients. The fluctuation of an ion concentration within the cytoplasm adjacent to the membrane channel can elicit an immediate, local response by altering the location and function of peripheral membrane proteins. Signals that affect a larger surface area of the cell membrane and/or persist over a prolonged time period will produce similarly cytoplasmic changes on larger spatial and time scales. We propose that as the amplitude, spatial extent, and duration of changes in cytoplasmic ion concentrations increase, the information can be communicated to the nucleus and other intracellular structure through ion flows along elements of the cytoskeleton to the centrosome (via microtubules) or proteins in the nuclear membrane (via microfilaments). These dynamics add spatial and temporal context to the more well-recognized information communication from the cell membrane to the nucleus following ligand binding to membrane receptors. Here, the signal is transmitted and amplified through transduction by the canonical molecular (e.g., Mitogen Activated Protein Kinases (MAPK) pathways. Cytoplasmic diffusion allows this information to be broadly distributed to intracellular organelles but at the cost of loss of spatial and temporal information also contained in ligand binding.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms20153609</identifier><identifier>PMID: 31344783</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Amino acids ; Calcium - metabolism ; Cell Communication - genetics ; cell membrane ; Cell Membrane - genetics ; Cell membranes ; Cell Nucleus - genetics ; Cellular structure ; Critical components ; Cytoplasm - genetics ; Cytoskeleton - genetics ; Deoxyribonucleic acid ; distributed system ; DNA ; DNA structure ; Dynamic structural analysis ; E coli ; Eukaryotic Cells ; Genes ; genome ; Genome - genetics ; Genomes ; Hypotheses ; information ; Information processing ; Information storage ; Ion Channels - genetics ; Ion Channels - metabolism ; Ions - metabolism ; Lipids ; Membranes ; Organisms ; Physiology ; Proteins ; Review ; signal conduction ; Signal Transduction - genetics ; Structure-function relationships</subject><ispartof>International journal of molecular sciences, 2019-07, Vol.20 (15), p.3609</ispartof><rights>2019. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the author. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-d7514717fc5e3fc769536d6f6a9f61fe3338a147a9a408dab98f25ff807d70a53</citedby><cites>FETCH-LOGICAL-c478t-d7514717fc5e3fc769536d6f6a9f61fe3338a147a9a408dab98f25ff807d70a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2333650561/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2333650561?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31344783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gatenby, Robert A</creatorcontrib><title>The Role of Cell Membrane Information Reception, Processing, and Communication in the Structure and Function of Multicellular Tissue</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Investigations of information dynamics in eukaryotic cells focus almost exclusively on heritable information in the genome. Gene networks are modeled as "central processors" that receive, analyze, and respond to intracellular and extracellular signals with the nucleus described as a cell's control center. Here, we present a model in which cellular information is a distributed system that includes non-genomic information processing in the cell membrane that may quantitatively exceed that of the genome. Within this model, the nucleus largely acts a source of macromolecules and processes information needed to synchronize their production with temporal variations in demand. However, the nucleus cannot produce microsecond responses to acute, life-threatening perturbations and cannot spatially resolve incoming signals or direct macromolecules to the cellular regions where they are needed. In contrast, the cell membrane, as the interface with its environment, can rapidly detect, process, and respond to external threats and opportunities through the large amounts of potential information encoded within the transmembrane ion gradient. Our model proposes environmental information is detected by specialized protein gates within ion-specific transmembrane channels. When the gate receives a specific environmental signal, the ion channel opens and the received information is communicated into the cell via flow of a specific ion species (i.e., K
, Na
, Cl
, Ca
, Mg
) along electrochemical gradients. The fluctuation of an ion concentration within the cytoplasm adjacent to the membrane channel can elicit an immediate, local response by altering the location and function of peripheral membrane proteins. Signals that affect a larger surface area of the cell membrane and/or persist over a prolonged time period will produce similarly cytoplasmic changes on larger spatial and time scales. We propose that as the amplitude, spatial extent, and duration of changes in cytoplasmic ion concentrations increase, the information can be communicated to the nucleus and other intracellular structure through ion flows along elements of the cytoskeleton to the centrosome (via microtubules) or proteins in the nuclear membrane (via microfilaments). These dynamics add spatial and temporal context to the more well-recognized information communication from the cell membrane to the nucleus following ligand binding to membrane receptors. Here, the signal is transmitted and amplified through transduction by the canonical molecular (e.g., Mitogen Activated Protein Kinases (MAPK) pathways. Cytoplasmic diffusion allows this information to be broadly distributed to intracellular organelles but at the cost of loss of spatial and temporal information also contained in ligand binding.</description><subject>Amino acids</subject><subject>Calcium - metabolism</subject><subject>Cell Communication - genetics</subject><subject>cell membrane</subject><subject>Cell Membrane - genetics</subject><subject>Cell membranes</subject><subject>Cell Nucleus - genetics</subject><subject>Cellular structure</subject><subject>Critical components</subject><subject>Cytoplasm - genetics</subject><subject>Cytoskeleton - genetics</subject><subject>Deoxyribonucleic acid</subject><subject>distributed system</subject><subject>DNA</subject><subject>DNA structure</subject><subject>Dynamic structural analysis</subject><subject>E coli</subject><subject>Eukaryotic Cells</subject><subject>Genes</subject><subject>genome</subject><subject>Genome - genetics</subject><subject>Genomes</subject><subject>Hypotheses</subject><subject>information</subject><subject>Information processing</subject><subject>Information storage</subject><subject>Ion Channels - genetics</subject><subject>Ion Channels - metabolism</subject><subject>Ions - metabolism</subject><subject>Lipids</subject><subject>Membranes</subject><subject>Organisms</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Review</subject><subject>signal conduction</subject><subject>Signal Transduction - genetics</subject><subject>Structure-function relationships</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdks1vEzEQxVcIREvhxhlZ4sIhAX-svbsXpCqiEKkVqISzNfGOU0e7drDXSNz5w3GSUqWcPPL89ObN01TVa0bfC9HRD247Jk6ZFIp2T6pzVnM-p1Q1T0_qs-pFSltKueCye16dCSbqumnFefVndYfkNgxIgiULHAZyg-M6gkey9DbEESYXPLlFg7t9NSPfYjCYkvObGQHfk0UYx-ydOYLOk6kofp9iNlOOeECusjeHbplxk4fJmTIoDxDJyqWU8WX1zMKQ8NX9e1H9uPq0WnyZX3_9vFxcXs9NMTvN-0ayumGNNRKFNY3qytK9sgo6q5hFIUQLhYAOatr2sO5ay6W1LW36hoIUF9XyqNsH2OpddCPE3zqA04ePEDcaYnE3oGYgQawBaS9tbaFupbTCCtq2tLNszYrWx6PWLq9H7A36KcLwSPRxx7s7vQm_tFKdEoIXgXf3AjH8zJgmPbq0D6ZkH3LSnCvZFLhWBX37H7oNOfoSleZlaSWpVHtHsyNlYkgpon0ww6jen4o-PZWCvzld4AH-dxviL6XKu6g</recordid><startdate>20190724</startdate><enddate>20190724</enddate><creator>Gatenby, Robert A</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20190724</creationdate><title>The Role of Cell Membrane Information Reception, Processing, and Communication in the Structure and Function of Multicellular Tissue</title><author>Gatenby, Robert A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-d7514717fc5e3fc769536d6f6a9f61fe3338a147a9a408dab98f25ff807d70a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Amino acids</topic><topic>Calcium - metabolism</topic><topic>Cell Communication - genetics</topic><topic>cell membrane</topic><topic>Cell Membrane - genetics</topic><topic>Cell membranes</topic><topic>Cell Nucleus - genetics</topic><topic>Cellular structure</topic><topic>Critical components</topic><topic>Cytoplasm - genetics</topic><topic>Cytoskeleton - genetics</topic><topic>Deoxyribonucleic acid</topic><topic>distributed system</topic><topic>DNA</topic><topic>DNA structure</topic><topic>Dynamic structural analysis</topic><topic>E coli</topic><topic>Eukaryotic Cells</topic><topic>Genes</topic><topic>genome</topic><topic>Genome - genetics</topic><topic>Genomes</topic><topic>Hypotheses</topic><topic>information</topic><topic>Information processing</topic><topic>Information storage</topic><topic>Ion Channels - genetics</topic><topic>Ion Channels - metabolism</topic><topic>Ions - metabolism</topic><topic>Lipids</topic><topic>Membranes</topic><topic>Organisms</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Review</topic><topic>signal conduction</topic><topic>Signal Transduction - genetics</topic><topic>Structure-function relationships</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gatenby, Robert A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gatenby, Robert A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Role of Cell Membrane Information Reception, Processing, and Communication in the Structure and Function of Multicellular Tissue</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2019-07-24</date><risdate>2019</risdate><volume>20</volume><issue>15</issue><spage>3609</spage><pages>3609-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Investigations of information dynamics in eukaryotic cells focus almost exclusively on heritable information in the genome. Gene networks are modeled as "central processors" that receive, analyze, and respond to intracellular and extracellular signals with the nucleus described as a cell's control center. Here, we present a model in which cellular information is a distributed system that includes non-genomic information processing in the cell membrane that may quantitatively exceed that of the genome. Within this model, the nucleus largely acts a source of macromolecules and processes information needed to synchronize their production with temporal variations in demand. However, the nucleus cannot produce microsecond responses to acute, life-threatening perturbations and cannot spatially resolve incoming signals or direct macromolecules to the cellular regions where they are needed. In contrast, the cell membrane, as the interface with its environment, can rapidly detect, process, and respond to external threats and opportunities through the large amounts of potential information encoded within the transmembrane ion gradient. Our model proposes environmental information is detected by specialized protein gates within ion-specific transmembrane channels. When the gate receives a specific environmental signal, the ion channel opens and the received information is communicated into the cell via flow of a specific ion species (i.e., K
, Na
, Cl
, Ca
, Mg
) along electrochemical gradients. The fluctuation of an ion concentration within the cytoplasm adjacent to the membrane channel can elicit an immediate, local response by altering the location and function of peripheral membrane proteins. Signals that affect a larger surface area of the cell membrane and/or persist over a prolonged time period will produce similarly cytoplasmic changes on larger spatial and time scales. We propose that as the amplitude, spatial extent, and duration of changes in cytoplasmic ion concentrations increase, the information can be communicated to the nucleus and other intracellular structure through ion flows along elements of the cytoskeleton to the centrosome (via microtubules) or proteins in the nuclear membrane (via microfilaments). These dynamics add spatial and temporal context to the more well-recognized information communication from the cell membrane to the nucleus following ligand binding to membrane receptors. Here, the signal is transmitted and amplified through transduction by the canonical molecular (e.g., Mitogen Activated Protein Kinases (MAPK) pathways. Cytoplasmic diffusion allows this information to be broadly distributed to intracellular organelles but at the cost of loss of spatial and temporal information also contained in ligand binding.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31344783</pmid><doi>10.3390/ijms20153609</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2019-07, Vol.20 (15), p.3609 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_1a5a3bae0d5f4fa4855f3f308809f1b1 |
source | Publicly Available Content Database; PubMed Central |
subjects | Amino acids Calcium - metabolism Cell Communication - genetics cell membrane Cell Membrane - genetics Cell membranes Cell Nucleus - genetics Cellular structure Critical components Cytoplasm - genetics Cytoskeleton - genetics Deoxyribonucleic acid distributed system DNA DNA structure Dynamic structural analysis E coli Eukaryotic Cells Genes genome Genome - genetics Genomes Hypotheses information Information processing Information storage Ion Channels - genetics Ion Channels - metabolism Ions - metabolism Lipids Membranes Organisms Physiology Proteins Review signal conduction Signal Transduction - genetics Structure-function relationships |
title | The Role of Cell Membrane Information Reception, Processing, and Communication in the Structure and Function of Multicellular Tissue |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T03%3A52%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Role%20of%20Cell%20Membrane%20Information%20Reception,%20Processing,%20and%20Communication%20in%20the%20Structure%20and%20Function%20of%20Multicellular%20Tissue&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Gatenby,%20Robert%20A&rft.date=2019-07-24&rft.volume=20&rft.issue=15&rft.spage=3609&rft.pages=3609-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms20153609&rft_dat=%3Cproquest_doaj_%3E2265766946%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c478t-d7514717fc5e3fc769536d6f6a9f61fe3338a147a9a408dab98f25ff807d70a53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2333650561&rft_id=info:pmid/31344783&rfr_iscdi=true |