AMPK Activation Can Promote Cardiac Differentiationby S timulating Autophagy Pathway

سال انتشار: 1401
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 107

نسخه کامل این مقاله ارائه نشده است و در دسترس نمی باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

RROYAN23_267

تاریخ نمایه سازی: 17 دی 1401

چکیده مقاله:

Objective: It has been shown that autophagy, an essentialcatabolic process for survival under s tress, contributes to differentiationinto various types of cells such as cardiomyocytes.Adenosine ۵ʹ-monophosphate (AMP)-activated protein kinase(AMPK) is an energy-sensing protein kinase involved in the regulation of autophagy. It has been demons trated that AMPKplays a role in many other cellular processes. Due to its involvementin multiple cellular processes, AMPK can influence thesurvival and health of cardiomyocytes. In this s tudy, the timedependenteffects of an activator of AMPK (Metformin) and anautophagy inhibitor (Hydroxychloroquine) on human pluripotents tem cell-derived cardiomyocytes (hPSC-CM) differentiationwere inves tigated.Materials and Methods: During cardiomyocyte differentiation,Metformin and Hydroxychloroquine were used to induceand inhibit autophagy, respectively. Days ۰, ۲, ۴, and ۱۳ wereexamined for the expression patterns of the autophagy genes.Results: During cardiomyocyte differentiation, autophagy wasupregulated, and it was not affected by autophagy inhibitor/inducer.AMPK activation also increased the expression of cardiomyocyte-specific markers in hPSC-CMs. Also, autophagy inhibitionby targeting autophagosome-lysosome fusion impairedcardiomyocyte differentiation.Conclusion: In conclusion, AMPK might be a promising targetfor regulating cardiomyocyte generation by in vitro differentiationof pluripotent s tem cells, due to the importance of autophagyin this cellular process.

کلیدواژه ها:

Autophagy ، Adenosine ۵ʹ-monophosphate-activatedprotein kinase (AMPK) ، Cardiomyocyte Differentiation ، HumanPluripotent S tem Cell (hPSC)

نویسندگان

M Kolahdouz Mohammadi

Department of Biology, School of Basic Science, Science andResearch Branch, Islamic Azad University, Tehran, Iran . Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cell Biology andTechnology, AC

S Pahlavan

Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cell Biology andTechnology, ACECR, Tehran, Iran

N Salehi

School of Biological Science, Ins titute for Research in FundamentalSciences (IPM), Tehran, Iran

F SotoodehnejadNematalah

Department of Biology, School of Basic Science, Science andResearch Branch, Islamic Azad University, Tehran, Iran

M Totonchi

Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cell Biology andTechnology, ACECR, Tehran, Iran