Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of Cajal

Abstract Transplantation of neural stem cells is a promising approach in treatment of intestinal dysfunctionality. The interstitial cells of Cajal (ICCs) are also critical in conditions such as pyloric dysfunctionality and gastroparesis. The objective of this study was to replenish neurons and ICCs...

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Main Authors: Prabhash Dadhich, Khalil N. Bitar
Format: Article
Language:English
Published: Wiley 2020-06-01
Series:Stem Cells Translational Medicine
Subjects:
Online Access:https://doi.org/10.1002/sctm.19-0316
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spelling doaj-ed1222305a43408b8ef9ce91b61a8d912020-11-25T03:10:42ZengWileyStem Cells Translational Medicine2157-65642157-65802020-06-019671372310.1002/sctm.19-0316Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of CajalPrabhash Dadhich0Khalil N. Bitar1Wake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine Winston‐Salem North CarolinaWake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine Winston‐Salem North CarolinaAbstract Transplantation of neural stem cells is a promising approach in treatment of intestinal dysfunctionality. The interstitial cells of Cajal (ICCs) are also critical in conditions such as pyloric dysfunctionality and gastroparesis. The objective of this study was to replenish neurons and ICCs in a dysfunctional pylorus as cell‐based therapy to restore functionality. ICCs and enteric neural progenitor cells (NPCs) were isolated from rat duodenum and transduced with fluorescent proteins. Rat pylorus was harvested, and an ex‐vivo neuromuscular dysfunctional model was developed by selective ablation of neurons and ICCs via chemical treatments. Cellular repopulation and restoration of motility were assessed by immunohistochemistry, qPCR, and functional analysis after delivery of fluorescently tagged cells. Chemical treatment of pylorus resulted in significant depletion of ICCs (67%, P = .0024; n = 3) and neural cells (83%, P = .0012; n = 3). Delivered ICCs and NPCs survived and integrated with host muscle layers. Co‐injection of ICCs with NPCs exhibited 34.4% (P = .0004; n = 3) and 61.0% (P = .0003; n = 3) upregulation of ANO1 and βIII tubulin, respectively. This regeneration resulted in the restoration of agonist‐induced excitatory contraction (82%) and neuron evoked relaxation (83%). The functional studies with specific neuronal nitric oxide (NO) synthase blocker confirmed that restoration of relaxation was NO mediated and neuronally derived. The simultaneous delivery of ICCs observed 35.7% higher neuronal differentiation and functional restoration compared with injection of NPCs alone. Injected NPCs and ICCs integrated into the dysfunctional ex vivo pylorus tissues and restored neuromuscular functionality. The co‐transplantation of NPCs and ICCs can be used to treat neurodegenerative disorders of the pylorus.https://doi.org/10.1002/sctm.19-0316cell interactionscell transplantationcellular therapydifferentiationexperimental modelsneural differentiation
collection DOAJ
language English
format Article
sources DOAJ
author Prabhash Dadhich
Khalil N. Bitar
spellingShingle Prabhash Dadhich
Khalil N. Bitar
Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of Cajal
Stem Cells Translational Medicine
cell interactions
cell transplantation
cellular therapy
differentiation
experimental models
neural differentiation
author_facet Prabhash Dadhich
Khalil N. Bitar
author_sort Prabhash Dadhich
title Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of Cajal
title_short Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of Cajal
title_full Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of Cajal
title_fullStr Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of Cajal
title_full_unstemmed Functional restoration of ex vivo model of pylorus: Co‐injection of neural progenitor cells and interstitial cells of Cajal
title_sort functional restoration of ex vivo model of pylorus: co‐injection of neural progenitor cells and interstitial cells of cajal
publisher Wiley
series Stem Cells Translational Medicine
issn 2157-6564
2157-6580
publishDate 2020-06-01
description Abstract Transplantation of neural stem cells is a promising approach in treatment of intestinal dysfunctionality. The interstitial cells of Cajal (ICCs) are also critical in conditions such as pyloric dysfunctionality and gastroparesis. The objective of this study was to replenish neurons and ICCs in a dysfunctional pylorus as cell‐based therapy to restore functionality. ICCs and enteric neural progenitor cells (NPCs) were isolated from rat duodenum and transduced with fluorescent proteins. Rat pylorus was harvested, and an ex‐vivo neuromuscular dysfunctional model was developed by selective ablation of neurons and ICCs via chemical treatments. Cellular repopulation and restoration of motility were assessed by immunohistochemistry, qPCR, and functional analysis after delivery of fluorescently tagged cells. Chemical treatment of pylorus resulted in significant depletion of ICCs (67%, P = .0024; n = 3) and neural cells (83%, P = .0012; n = 3). Delivered ICCs and NPCs survived and integrated with host muscle layers. Co‐injection of ICCs with NPCs exhibited 34.4% (P = .0004; n = 3) and 61.0% (P = .0003; n = 3) upregulation of ANO1 and βIII tubulin, respectively. This regeneration resulted in the restoration of agonist‐induced excitatory contraction (82%) and neuron evoked relaxation (83%). The functional studies with specific neuronal nitric oxide (NO) synthase blocker confirmed that restoration of relaxation was NO mediated and neuronally derived. The simultaneous delivery of ICCs observed 35.7% higher neuronal differentiation and functional restoration compared with injection of NPCs alone. Injected NPCs and ICCs integrated into the dysfunctional ex vivo pylorus tissues and restored neuromuscular functionality. The co‐transplantation of NPCs and ICCs can be used to treat neurodegenerative disorders of the pylorus.
topic cell interactions
cell transplantation
cellular therapy
differentiation
experimental models
neural differentiation
url https://doi.org/10.1002/sctm.19-0316
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