Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 Polarization

ABSTRACT Background Chronic refractory wounds refer to wounds that cannot be repaired timely. Platelet‐rich plasma (PRP) has significant potential in chronic wound healing therapy. The exosomes isolated from PRP were proved to exhibit more effectiveness than PRP. However, the therapeutic potential o...

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Main Authors: Xiong Li, Feifei Guo, Jiehua Deng, Jiasong Li, Jie Zhang, Ming Fu, Hui Fan
Format: Article
Language:English
Published: Wiley 2024-11-01
Series:Immunity, Inflammation and Disease
Subjects:
Online Access:https://doi.org/10.1002/iid3.70064
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author Xiong Li
Feifei Guo
Jiehua Deng
Jiasong Li
Jie Zhang
Ming Fu
Hui Fan
author_facet Xiong Li
Feifei Guo
Jiehua Deng
Jiasong Li
Jie Zhang
Ming Fu
Hui Fan
author_sort Xiong Li
collection DOAJ
description ABSTRACT Background Chronic refractory wounds refer to wounds that cannot be repaired timely. Platelet‐rich plasma (PRP) has significant potential in chronic wound healing therapy. The exosomes isolated from PRP were proved to exhibit more effectiveness than PRP. However, the therapeutic potential of exosomes from PRP on chronic refractory wounds remained elusive. Hence, this study aimed to clarify the action of exosomes from PRP on chronic refractory wounds by evaluating the response of macrophages to exosomes. Methods Pure platelet‐rich plasma (P‐PRP) and leukocyte platelet‐rich plasma (L‐PRP) were prepared from the fasting venous blood of healthy volunteers. Exosomes were extracted from P‐PRP and L‐PRP using ultracentrifugation and identified by transmission electron microscopy (TEM), nanoparticle tracking analysis (NTA), and western blot. Macrophages were obtained by inducing THP‐1 cells with phorbol‐12‐myristate‐13 acetate (PMA). The internalization of exosomes into macrophages was observed utilizing confocal laser scanning microscopy after being labeled with PKH67. Cell viability was determined by CCK‐8 assay. Cell apoptosis was measured utilizing a flow cytometer. The polarization status of M1 and M2 macrophages were evaluated by detecting their markers. Nitric oxide (NO) detection was conducted using the commercial kit. Results Exosomes from P‐PRP and L‐PRP were absorbed by macrophages. Exosomes from L‐PRP restrained viability and induced apoptosis of macrophages. Besides, exosomes from P‐PRP promoted M2 polarization, and exosomes from L‐PRP promoted M1 polarization. Furthermore, exosomes from L‐PRP promoted NO generation of macrophages. Conclusion Exosomes from L‐PRP restrained viability, induced apoptosis and NO generation of macrophages, and promoted M1 polarization, while exosomes from P‐PRP increased M2 polarization. The exosomes from L‐PRP presented a more effective effect on macrophages than that from P‐PRP, making it a promising strategy for chronic refractory wound management.
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spelling doaj-art-bb03aa2010c04f7a99ed36a5f91c31ae2025-08-20T02:11:00ZengWileyImmunity, Inflammation and Disease2050-45272024-11-011211n/an/a10.1002/iid3.70064Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 PolarizationXiong Li0Feifei Guo1Jiehua Deng2Jiasong Li3Jie Zhang4Ming Fu5Hui Fan6Department of Plastic and Aesthetic Surgery The Second Affiliated Hospital of Guilin Medical University Guilin ChinaDepartment of Health Management Centre The Second Affiliated Hospital of Guilin Medical University Guilin ChinaDepartment of Plastic and Aesthetic Surgery The Second Affiliated Hospital of Guilin Medical University Guilin ChinaDepartment of Plastic and Aesthetic Surgery The Second Affiliated Hospital of Guilin Medical University Guilin ChinaDepartment of Plastic and Aesthetic Surgery The Second Affiliated Hospital of Guilin Medical University Guilin ChinaDepartment of Plastic and Aesthetic Surgery The Second Affiliated Hospital of Guilin Medical University Guilin ChinaDepartment of Otolaryngology The Second Affiliated Hospital of Guilin Medical University Guilin ChinaABSTRACT Background Chronic refractory wounds refer to wounds that cannot be repaired timely. Platelet‐rich plasma (PRP) has significant potential in chronic wound healing therapy. The exosomes isolated from PRP were proved to exhibit more effectiveness than PRP. However, the therapeutic potential of exosomes from PRP on chronic refractory wounds remained elusive. Hence, this study aimed to clarify the action of exosomes from PRP on chronic refractory wounds by evaluating the response of macrophages to exosomes. Methods Pure platelet‐rich plasma (P‐PRP) and leukocyte platelet‐rich plasma (L‐PRP) were prepared from the fasting venous blood of healthy volunteers. Exosomes were extracted from P‐PRP and L‐PRP using ultracentrifugation and identified by transmission electron microscopy (TEM), nanoparticle tracking analysis (NTA), and western blot. Macrophages were obtained by inducing THP‐1 cells with phorbol‐12‐myristate‐13 acetate (PMA). The internalization of exosomes into macrophages was observed utilizing confocal laser scanning microscopy after being labeled with PKH67. Cell viability was determined by CCK‐8 assay. Cell apoptosis was measured utilizing a flow cytometer. The polarization status of M1 and M2 macrophages were evaluated by detecting their markers. Nitric oxide (NO) detection was conducted using the commercial kit. Results Exosomes from P‐PRP and L‐PRP were absorbed by macrophages. Exosomes from L‐PRP restrained viability and induced apoptosis of macrophages. Besides, exosomes from P‐PRP promoted M2 polarization, and exosomes from L‐PRP promoted M1 polarization. Furthermore, exosomes from L‐PRP promoted NO generation of macrophages. Conclusion Exosomes from L‐PRP restrained viability, induced apoptosis and NO generation of macrophages, and promoted M1 polarization, while exosomes from P‐PRP increased M2 polarization. The exosomes from L‐PRP presented a more effective effect on macrophages than that from P‐PRP, making it a promising strategy for chronic refractory wound management.https://doi.org/10.1002/iid3.70064apoptosischronic refractory woundsL‐PRPmacrophagesNOpolarization
spellingShingle Xiong Li
Feifei Guo
Jiehua Deng
Jiasong Li
Jie Zhang
Ming Fu
Hui Fan
Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 Polarization
Immunity, Inflammation and Disease
apoptosis
chronic refractory wounds
L‐PRP
macrophages
NO
polarization
title Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 Polarization
title_full Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 Polarization
title_fullStr Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 Polarization
title_full_unstemmed Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 Polarization
title_short Leukocyte Platelet‐Rich Plasma‐Derived Exosomes Restrained Macrophages Viability and Induced Apoptosis, NO Generation, and M1 Polarization
title_sort leukocyte platelet rich plasma derived exosomes restrained macrophages viability and induced apoptosis no generation and m1 polarization
topic apoptosis
chronic refractory wounds
L‐PRP
macrophages
NO
polarization
url https://doi.org/10.1002/iid3.70064
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