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1. Cardiac inducing RNAs (CIRs) from human fetal heart promote the differentiation of non-muscle cells to form into cardiomyocytes in vitro.

   https://doi.org/10.31031/AICS.2021.03.000553  

   Lemanski, L.F. (April 2021, Advancements in case studies)

   null (Ed.)

   We have discovered a cardiac-inducing RNA (CIR) in the axolotl, Ambystoma mexicanum, (a salamander) and two cardiac inducing RNAs (CIR-6 and CIR-30) in human heart that have the ability to induce the differentiation of non-muscle cells, including induced pluripotent stem cells from human skin, mouse embryonic stem cells, and mouse fibroblasts into cardiomyocytes in vitro. Although the primary sequences of salamander and human RNAs are not homologous, their secondary structures are very similar and we believe account for their shared unique abilities to promote differentiation of non-muscle cells into definitive cardiomyocytes. We are beginning to explore the potential for repair/regeneration of cardiac muscle in vivo using mouse and rat models with induced acute myocardial infarctions (AMI) to determine if pluripotent stem cells or fibroblasts transfected with the human CIRs or CIRs alone injected into the damaged areas of the hearts can effect repair of the damaged cardiac muscle tissue, and return the infarcted hearts and the AMI animal models to pre-heart-attack function again. If cardiac cells damaged in heart attacks can be replaced with living, functioning cardiomyocytes, patients with heart disease would be able to have normal heart function restored and could return to normal pre-heart-attack activity levels. Understanding how CIR transforms non-muscle cells into vigorously contracting, functional cardiac muscle and effectively replacing damaged heart cells with newly-formed cardiac muscle tissue would represent a major breakthrough in modern biology and medicine with the potential to have a significant impact on the survival rate and quality of life of millions of individuals worldwide who suffer heart attacks each year. 

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2. Monolithic silicon for high spatiotemporal translational photostimulation

   https://doi.org/10.1038/s41586-024-07016-9  

   Li, Pengju; Zhang, Jing; Hayashi, Hidenori; Yue, Jiping; Li, Wen; Yang, Chuanwang; Sun, Changxu; Shi, Jiuyun; Huberman-Shlaes, Judah; Hibino, Narutoshi; et al (February 2024, Nature)

   Electrode-based electrical stimulation underpins several clinical bioelectronic devices, including deep-brain stimulators and cardiac pacemakers. However, leadless multisite stimulation is constrained by the technical difficulties and spatial-access limitations of electrode arrays. Optogenetics offers optically controlled random access with high spatiotemporal capabilities, but clinical translation poses challenges. Here we show tunable spatiotemporal photostimulation of cardiac systems using a non-genetic platform based on semiconductor-enabled biomodulation interfaces. Through spatiotemporal profiling of photoelectrochemical currents, we assess the magnitude, precision, accuracy and resolution of photostimulation in four leadless silicon-based monolithic photoelectrochemical devices. We demonstrate the optoelectronic capabilities of the devices through optical overdrive pacing of cultured cardiomyocytes (CMs) targeting several regions and spatial extents, isolated rat hearts in a Langendorff apparatus, in vivo rat hearts in an ischaemia model and an in vivo mouse heart model with transthoracic optical pacing. We also perform the first, to our knowledge, optical override pacing and multisite pacing of a pig heart in vivo. Our systems are readily adaptable for minimally invasive clinical procedures using our custom endoscopic delivery device, with which we demonstrate closed-thoracic operations and endoscopic optical stimulation. Our results indicate the clinical potential of the leadless, lightweight and multisite photostimulation platform as a pacemaker in cardiac resynchronization therapy (CRT), in which lead-placement complications are common. 

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3. Mechanical Stress Triggers Premature Senescence in Cardiac Fibroblasts

   https://doi.org/10.1002/advs.202513314  

   Schneider, Stephanie_E; Scott, Adrienne_K; Gallagher, Katie_M; Miller, Emily_Y; Ghosh, Soham; Neu, Corey_P (September 2025, Advanced Science)

   Abstract The cardiovascular system functions under continuous cyclic mechanical stretch, with disruptions in mechanical and biochemical signals contributing to disease progression. In cardiovascular disorders, these disruptions activate cardiac fibroblasts (CFs) and promote cellular senescence, yet it remains unclear whether mechanical stimuli alone can initiate this phenotype. Here, primary murine CFs are exposed to uniaxial stretch, and systematically varied mechanical parameters assessed their role in senescence induction. Loss of stretch magnitude and increase in frequency, mimicking a pathologic hypertrophy and fibrosis, led to a senescence phenotype, identified through cell cycle arrest, decreased lamin B expression, and DNA damage. Mechanically‐induced CF senescence depends on p53/p21, whereas senescence triggered by oxidative stress or lamin A/C mutation proceeded via p16. Notably, mechanically‐induced premature senescence is accompanied by reduced levels of the nuclear envelope protein emerin. These findings demonstrate that altered mechanical signals are sufficient to trigger premature senescence and implicate compromised nuclear integrity in the underlying mechanism. 

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4. Evaluating Passive Myocardial Stiffness Using in vivo cine, cDTI, and Tagged MRI

   https://doi.org/10.1007/978-3-031-35302-4_54  

   Kolawole, Fikunwa O.; Wang, Vicky Y.; Freytag, Bianca; Loecher, Michael; Cork, Tyler E.; Nash, Martyn P.; Kuhl, Ellen; Ennis, Daniel B. (June 2023, Functional Imaging and Modeling of the Heart. FIMH 2023. Lecture Notes in Computer Science.)

   Bernard, O.; Clarysse, P.; Duchateau, N.; Ohayon, J.; Viallon, M (Ed.)

   Increased passive myocardial stiffness is implicated in the pathophysiology of many cardiac diseases, and its in vivo estimation can improve management of heart disease. MRI-driven computational constitutive modeling has been used extensively to evaluate passive myocardial stiffness. This approach requires subject-specific data that is best acquired with different MRI sequences: conventional cine (e.g. bSSFP), tagged MRI (or DENSE), and cardiac diffusion tensor imaging. However, due to the lack of comprehensive datasets and the challenge of incorporating multi-phase and single-phase disparate MRI data, no studies have combined in vivo cine bSSFP, tagged MRI, and cardiac diffusion tensor imaging to estimate passive myocardial stiffness. The objective of this work was to develop a personalized in silico left ventricular model to evaluate passive myocardial stiffness by integrating subject-specific geometric data derived from cine bSSFP, regional kinematics extracted from tagged MRI, and myocardial microstructure measured using in vivo cardiac diffusion tensor imaging. To demonstrate the feasibility of using a complete subject-specific imaging dataset for passive myocardial stiffness estimation, we calibrated a bulk stiffness parameter of a transversely isotropic exponential constitutive relation to match the local kinematic field extracted from tagged MRI. This work establishes a pipeline for developing subject-specific biomechanical ventricular models to probe passive myocardial mechanical behavior, using comprehensive cardiac imaging data from multiple in vivo MRI sequences. 

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5. Development of Novel Carbon Fiber based Electrodes for Lithium-ion Batteries

   Kaynan, Ozge; Raj, Ayush; Carrola, Mia; Castaneda, Homero; Asadi, Amir (September 2023, American Society for Composites-DESTech publications)

   Carbon fiber-based structural lithium-ion batteries are attracting significant attention in the automotive and aerospace industries due to their dual capability of energy storage and mechanical load-bearing, leading to weight reduction. These batteries utilize lightweight carbon fiber (CF) composites, which offer excellent stiffness, strength-to-weight ratios, and electrical conductivity. Polyacrylonitrile-based CFs, comprising graphitic and amorphous carbon, are particularly suitable for Li-ion battery applications as they allow the storage of lithium ions. However, integrating lithium iron phosphate (LFP) into CFs poses challenges due to complex lab-scale processes and the use of toxic dispersants, hindering large-scale industrial compatibility. To address this, we investigate the development of water-based LFP-integrated CF structural Li-ion batteries. Homogeneous suspensions are created using cellulose nanocrystals (CNCs) to form hybrid structures. The battery system employs LFP-modified CF as the cathode, unsized CF as the anode, and a water-based electrolyte. The LFP-CNC-graphene nanoplatelet (GNP) hybrids are coated onto CFs through immersion coating. Scanning electron microscopy (SEM) images confirm the well-dispersed and well-adhered LFP-CNC-GNP structures on the CF surface, contributing to their mechanical interlocking and electrochemical performance. The batteries demonstrate a specific energy density of 62.67 Wh/kg and a specific capacity of 72.7 mAh/g. Furthermore, the cyclic voltammetry experiments reveal the stability of the LFP-CNC-GNP-coated CF batteries over 200 cycles without degradation. This research enables the engineering of hybrid nanostructured battery laminates using novel LFP-CNC-GNP-coated CFs, opening avenues for the development of innovative Li-ion structural batteries. 

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