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Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body

Fluid in interstitial spaces accounts for ~20% of an adult body weight and flows diffusively for a short range. Does it circulate around the body like vascular circulations? This bold conjecture has been debated for decades. As a conventional physiological concept, interstitial space is a micron‐siz...

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Autores principales: Li, Hongyi, Yin, Yajun, Yang, Chongqing, Chen, Min, Wang, Fang, Ma, Chao, Li, Hua, Kong, Yiya, Ji, Fusui, Hu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046480/
https://www.ncbi.nlm.nih.gov/pubmed/31957194
http://dx.doi.org/10.1111/cpr.12760
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author Li, Hongyi
Yin, Yajun
Yang, Chongqing
Chen, Min
Wang, Fang
Ma, Chao
Li, Hua
Kong, Yiya
Ji, Fusui
Hu, Jun
author_facet Li, Hongyi
Yin, Yajun
Yang, Chongqing
Chen, Min
Wang, Fang
Ma, Chao
Li, Hua
Kong, Yiya
Ji, Fusui
Hu, Jun
author_sort Li, Hongyi
collection PubMed
description Fluid in interstitial spaces accounts for ~20% of an adult body weight and flows diffusively for a short range. Does it circulate around the body like vascular circulations? This bold conjecture has been debated for decades. As a conventional physiological concept, interstitial space is a micron‐sized space between cells and vasculature. Fluid in interstitial spaces is thought to be entrapped within interstitial matrix. However, our serial data have further defined a second space in interstitium that is a nanosized interfacial transport zone on a solid surface. Within this fine space, fluid along a solid fibre can be transported under a driving power and identically, interstitial fluid transport can be visualized by tracking the oriented fibres. Since 2006, our data from volunteers and cadavers have revealed a long‐distance extravascular pathway for interstitial fluid flow, comprising at least four types of anatomic distributions. The framework of each extravascular pathway contains the longitudinally assembled and oriented fibres, working as a fibrorail for fluid flow. Interestingly, our data showed that the movement of fluid in a fibrous pathway is in response to a dynamic driving source and named as dynamotaxis. By analysis of previous studies and our experimental results, a hypothesis of interstitial fluid circulatory system is proposed.
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spelling pubmed-70464802020-03-13 Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body Li, Hongyi Yin, Yajun Yang, Chongqing Chen, Min Wang, Fang Ma, Chao Li, Hua Kong, Yiya Ji, Fusui Hu, Jun Cell Prolif Review Fluid in interstitial spaces accounts for ~20% of an adult body weight and flows diffusively for a short range. Does it circulate around the body like vascular circulations? This bold conjecture has been debated for decades. As a conventional physiological concept, interstitial space is a micron‐sized space between cells and vasculature. Fluid in interstitial spaces is thought to be entrapped within interstitial matrix. However, our serial data have further defined a second space in interstitium that is a nanosized interfacial transport zone on a solid surface. Within this fine space, fluid along a solid fibre can be transported under a driving power and identically, interstitial fluid transport can be visualized by tracking the oriented fibres. Since 2006, our data from volunteers and cadavers have revealed a long‐distance extravascular pathway for interstitial fluid flow, comprising at least four types of anatomic distributions. The framework of each extravascular pathway contains the longitudinally assembled and oriented fibres, working as a fibrorail for fluid flow. Interestingly, our data showed that the movement of fluid in a fibrous pathway is in response to a dynamic driving source and named as dynamotaxis. By analysis of previous studies and our experimental results, a hypothesis of interstitial fluid circulatory system is proposed. John Wiley and Sons Inc. 2020-01-19 /pmc/articles/PMC7046480/ /pubmed/31957194 http://dx.doi.org/10.1111/cpr.12760 Text en © 2020 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Li, Hongyi
Yin, Yajun
Yang, Chongqing
Chen, Min
Wang, Fang
Ma, Chao
Li, Hua
Kong, Yiya
Ji, Fusui
Hu, Jun
Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body
title Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body
title_full Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body
title_fullStr Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body
title_full_unstemmed Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body
title_short Active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body
title_sort active interfacial dynamic transport of fluid in a network of fibrous connective tissues throughout the whole body
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046480/
https://www.ncbi.nlm.nih.gov/pubmed/31957194
http://dx.doi.org/10.1111/cpr.12760
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