Systemic Infusion of Expanded CD133+ Cells and Expanded CD133+ Cell-Derived EVs for the Treatment of Ischemic Cardiomyopathy in a Rat Model of AMI

المؤلفون المشاركون

Senegaglia, Alexandra Cristina
Angulski, Addeli B. B.
Capriglione, Luiz Guilherme A.
Barchiki, Fabiane
Brofman, Paulo
Stimamiglio, Marco A.
Correa, Alejandro

المصدر

Stem Cells International

العدد

المجلد 2019، العدد 2019 (31 ديسمبر/كانون الأول 2019)، ص ص. 1-11، 11ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2019-12-01

دولة النشر

مصر

عدد الصفحات

11

الملخص EN

Myocardial infarction is a leading cause of death among all cardiovascular diseases.

Cell therapies using a cell population enriched with endothelial progenitor cells (EPCs), expanded CD133+ cells, have promise as a therapeutic option for the treatment of ischemic areas after infarction.

Recently, secreted membrane vesicles, including exosomes and microvesicles, have been recognized as new therapeutic candidates with important roles in intercellular and tissue communication.

Expanded CD133+ cells have the ability to produce extracellular vesicles (EVs); however, their effect in the context of the heart is unknown.

In the present study, we evaluated the effectiveness of the systemic application of expanded CD133+ cells and expanded CD133+ cell-derived EVs for the treatment of ischemic cardiomyopathy in a rat model of acute myocardial infarction (AMI) and examined the hypothesis that the EVs, because of their critical role in transferring regenerative signals from stem cells to the injured tissues, might elicit an equal or better therapeutic response than the expanded CD133+ cells.

We demonstrate that the systemic application of expanded CD133+ cells and EVs has similar effects in infarcted rats.

Few animals per group showed improvements in several heart and kidney parameters analyzed, but not significant differences were observed when comparing the groups.

The systemic route may not be effective to treat ischemic cardiomyopathy; nonetheless, it may be a beneficial therapy to treat the side effects of AMI such as kidney damage.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Angulski, Addeli B. B.& Capriglione, Luiz Guilherme A.& Barchiki, Fabiane& Brofman, Paulo& Stimamiglio, Marco A.& Senegaglia, Alexandra Cristina…[et al.]. 2019. Systemic Infusion of Expanded CD133+ Cells and Expanded CD133+ Cell-Derived EVs for the Treatment of Ischemic Cardiomyopathy in a Rat Model of AMI. Stem Cells International،Vol. 2019, no. 2019, pp.1-11.
https://search.emarefa.net/detail/BIM-1208899

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Angulski, Addeli B. B.…[et al.]. Systemic Infusion of Expanded CD133+ Cells and Expanded CD133+ Cell-Derived EVs for the Treatment of Ischemic Cardiomyopathy in a Rat Model of AMI. Stem Cells International No. 2019 (2019), pp.1-11.
https://search.emarefa.net/detail/BIM-1208899

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Angulski, Addeli B. B.& Capriglione, Luiz Guilherme A.& Barchiki, Fabiane& Brofman, Paulo& Stimamiglio, Marco A.& Senegaglia, Alexandra Cristina…[et al.]. Systemic Infusion of Expanded CD133+ Cells and Expanded CD133+ Cell-Derived EVs for the Treatment of Ischemic Cardiomyopathy in a Rat Model of AMI. Stem Cells International. 2019. Vol. 2019, no. 2019, pp.1-11.
https://search.emarefa.net/detail/BIM-1208899

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1208899