Novel Insights into the Role of Heart Cells in Cardiac Function, Remodeling and Regeneration

A special issue of Biology (ISSN 2079-7737). This special issue belongs to the section "Medical Biology".

Deadline for manuscript submissions: closed (30 November 2021) | Viewed by 7248

Special Issue Editors


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Guest Editor
Vascular Biology and Regenerative Medicine Unit, Centro Cardiologico Monzino IRCCS, 20138 Milan, Italy
Interests: calcium signaling; CaMKII; cardiovascular diseases; arrhythmogenic cardiomyopathy; mesenchymal stromal cells; human-induced pluripotent stem-cell-derived cardiomyocytes

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Guest Editor
Laboratory of Cardiac Cellular Physiology, Department of Biotechnology and Biosciences, University of Milano-Bicocca, I-20126 Milan, Italy
Interests: cardiac cellular physiology; arrhythmias; nanotechnology; optical stimulation; Ca2+ signalling; excitation-contraction coupling
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Guest Editor
Centro de Investigaciones Cardiovasculares, University of La Plata (UNLP)-CONICET, Argentina
Interests: alkalinizing transporters and cardiac pathophysiology; arrhythmias; excitation–contraction coupling; ovariectomized rats

Special Issue Information

Dear Colleagues,

The heart is a multicellular organ with highly specialized structures and cells that communicate with each other through direct cell–cell interactions and paracrine signaling, contributing to an organized structure and proper function.

Understanding the signaling pathways involved in cardiac cell expansion, differentiation into a specific lineage, survival within the host tissue, and communication is of paramount importance to boosting their therapeutic application.

In fact, the concept that the heart is a regeneration-capable organ has highlighted the possibility that cell-based therapies may provide alternative, even more effective, treatments to conventional treatments for heart failure.

In parallel, the ability to differentiate human-induced pluripotent stem cells (hiPSCs) into cardiomyocytes (hiPSC-CMs) represents an inexhaustible and scalable source of differentiated patient-specific cells that carry the same genome as the subject they are derived from, thus representing a valuable in vitro tool for performing mechanistic investigations on specific cardiac diseases and for predictive safety pharmacology in a reliable human-derived screening model. Likewise, restoring coronary circulation by stimulating resident endothelial cells or injecting endothelial precursors could also promote cardiac repair.

We therefore strongly encourage the submission of original research articles, state-of-the-art reviews, and perspective papers that will highlight novel insights into the signaling pathways that drive the fate of cardiac cells and their therapeutic application for both structural and conduction cardiac disturbances. Potential topics for this Special Issue include, but are not limited to:

  • new perspectives on the role of endothelial progenitor cells (EPCs), mesenchymal stem cells (MSCs), and adipose-tissue-derived stem and progenitor cells (ADSCs) in cardiac remodeling and regeneration;
  • new perspectives on cardiac resident stem cells;
  • novel signaling pathways to boost therapeutic heart therapy interventions;
  • application of hiPSCs as a model of heart development for the study of congenital heart disease; and
  • innovative strategies for cardiac regeneration and disease modeling.

Dr. Angela Serena Maione
Dr. Francesco Lodola
Dr. Verónica C. De Giusti
Guest Editors

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Keywords

  • cardiovascular diseases;
  • signaling pathways;
  • cardiac cells;
  • cardiac regeneration;
  • cardiac remodeling;
  • arrhythmias.

Published Papers (2 papers)

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Review

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18 pages, 7964 KiB  
Review
Phenotypic and Functional Heterogeneity of Monocyte Subsets in Chronic Heart Failure Patients
by Aušra Mongirdienė and Julius Liobikas
Biology 2022, 11(2), 195; https://doi.org/10.3390/biology11020195 - 26 Jan 2022
Cited by 3 | Viewed by 3331
Abstract
Chronic heart failure (CHF) results when the heart cannot consistently supply the body’s tissues with oxygen and required nutrients. CHF can be categorized as heart failure (HF) with preserved ejection fraction (HFpEF) or HF with reduced ejection fraction (HFrEF). There are different causes [...] Read more.
Chronic heart failure (CHF) results when the heart cannot consistently supply the body’s tissues with oxygen and required nutrients. CHF can be categorized as heart failure (HF) with preserved ejection fraction (HFpEF) or HF with reduced ejection fraction (HFrEF). There are different causes and mechanisms underlying HF pathogenesis; however, inflammation can be regarded as one of the factors that promotes both HFrEF and HFpEF. Monocytes, a subgroup of leukocytes, are known to be cellular mediators in response to cardiovascular injury and are closely related to inflammatory reactions. These cells are a vital component of the immune system and are the source of macrophages, which participate in cardiac tissue repair after injury. However, these monocytes are not as homogenous as thought and can present different functions under different cardiovascular disease conditions. In addition, there is still an open question regarding whether the functions of monocytes and macrophages should be regarded as causes or consequences in CHF development. Therefore, the aim of this work was to summarize current studies on the functions of various monocyte subsets in CHF with a focus on the role of a certain monocyte subset in HFpEF and HFrEF patients, as well as the subsets’ relationship to inflammatory markers. Full article
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14 pages, 9813 KiB  
Perspective
Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
by Francesco Lodola, Verónica Celeste De Giusti, Claudia Maniezzi, Daniele Martone, Ilaria Stadiotti, Elena Sommariva and Angela Serena Maione
Biology 2021, 10(8), 730; https://doi.org/10.3390/biology10080730 - 30 Jul 2021
Cited by 1 | Viewed by 2947
Abstract
The stem cell technology and the induced pluripotent stem cells (iPSCs) production represent an excellent alternative tool to study cardiomyopathies, which overcome the limitations associated with primary cardiomyocytes (CMs) access and manipulation. CMs from human iPSCs (hiPSC–CMs) are genetically identical to patient primary [...] Read more.
The stem cell technology and the induced pluripotent stem cells (iPSCs) production represent an excellent alternative tool to study cardiomyopathies, which overcome the limitations associated with primary cardiomyocytes (CMs) access and manipulation. CMs from human iPSCs (hiPSC–CMs) are genetically identical to patient primary cells of origin, with the main electrophysiological and mechanical features of CMs. The key issue to be solved is to achieve a degree of structural and functional maturity typical of adult CMs. In this perspective, we will focus on the main differences between fetal-like hiPSC-CMs and adult CMs. A viewpoint is given on the different approaches used to improve hiPSC-CMs maturity, spanning from long-term culture to complex engineered heart tissue. Further, we outline limitations and future developments needed in cardiomyopathy disease modeling. Full article
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