Jeremy L. Herrmann

ORCID: 0000-0001-7818-0548
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About
Contact & Profiles
Research Areas
  • Congenital Heart Disease Studies
  • Mesenchymal stem cell research
  • Cardiac Ischemia and Reperfusion
  • Cardiac Valve Diseases and Treatments
  • Cardiac Structural Anomalies and Repair
  • Aortic Disease and Treatment Approaches
  • Pulmonary Hypertension Research and Treatments
  • Tissue Engineering and Regenerative Medicine
  • Tracheal and airway disorders
  • Mechanical Circulatory Support Devices
  • Cardiac Arrest and Resuscitation
  • Infective Endocarditis Diagnosis and Management
  • Coronary Artery Anomalies
  • Anesthesia and Neurotoxicity Research
  • Cardiac Fibrosis and Remodeling
  • Congenital heart defects research
  • Cytokine Signaling Pathways and Interactions
  • Transplantation: Methods and Outcomes
  • Electrospun Nanofibers in Biomedical Applications
  • Immune Response and Inflammation
  • Cardiac, Anesthesia and Surgical Outcomes
  • Estrogen and related hormone effects
  • Vascular anomalies and interventions
  • Clinical Nutrition and Gastroenterology
  • Cardiac Arrhythmias and Treatments

Indiana University – Purdue University Indianapolis
2011-2025

Children's Hospital of Philadelphia
2014-2025

Indiana University Health
2018-2025

Riley Hospital for Children
2018-2025

Indiana University School of Medicine
2010-2024

Houston Methodist
2023

Creative Commons
2022

Indiana University
2007-2022

University School
2022

Eastern Virginia Medical School
2022

Mesenchymal stem cells (MSCs) are a promising therapy for acute organ ischemia in part due to their paracrine production of growth factors. However, transplanted encounter an inflammatory environment that mitigates function and survival, treating the with exogenous agents during ex vivo expansion before transplantation is one strategy overcoming this limitation by enhancing function. We hypothesized preconditioning bone marrow MSCs TGF-alpha would 1) increase MSC critical factor, vascular...

10.1097/shk.0b013e3181b7d137 article EN Shock 2009-12-08

Bone marrow mesenchymal stem cells (MSCs) may be a novel treatment modality for organ ischemia, possibly through the release of beneficial paracrine factors. However, an age threshold likely exists as to when MSCs gain their protective properties. We hypothesized that 1) VEGF would crucial cell mediator in providing postischemic myocardial protection and 2) small-interfering (si)RNA ablation adult (aMSCs) equalize differences observed between aMSC- neonatal (nMSC)-mediated cardioprotection....

10.1152/ajpheart.00565.2008 article EN AJP Heart and Circulatory Physiology 2008-10-11

Females have a lower incidence of heart failure and improved survival after myocardial ischemia-reperfusion (I/R) compared with males. Although estrogen-suppressed cardiomyocyte apoptosis may be mediated through the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) pathway, it is unclear whether this action via estrogen receptor beta (ERbeta). Therefore, we hypothesized that ERbeta mediates estrogen-induced cardioprotection PI3K/Akt antiapoptotic signaling in females but not...

10.1152/ajpregu.00045.2009 article EN AJP Regulatory Integrative and Comparative Physiology 2009-02-12

Optimizing the function and proliferative capacity of stem cells is essential to maximize their therapeutic benefits. High glucose concentrations are known have detrimental effects on many cell types. We hypothesized that human mesenchymal (hMSCs) cultured in high glucose-containing media would exhibit diminished proliferation attenuated production VEGF, hepatocyte growth factor (HGF), FGF2 response treatment with TNF-alpha, LPS, or hypoxia. hMSCs were plated medium containing low (5.5 mM)...

10.1152/ajpregu.90876.2008 article EN AJP Regulatory Integrative and Comparative Physiology 2009-04-22

Mesenchymal stem cells (MSCs) possess immunomodulatory properties and may curtail the inflammatory response that characterizes sepsis other systemic states. We aimed to determine whether intravenous infusion of MSCs is associated with reduced inflammation improved myocardial function in a rat model endotoxemia. Adult Sprague-Dawley rats were administered saline (vehicle) or LPS (5 mg/kg) via tail vein injection. Treatments, either vehicle 2 × 10(6) MSCs, infused 1 h later vein. Animals...

10.1097/shk.0b013e318225f6ae article EN Shock 2011-06-08

Optimal right ventricle-to-pulmonary artery (RV-PA) conduit size for patients with truncus arteriosus is controversial. We aimed to determine the relationship between branch PA and need reoperation following repair of arteriosus. performed a single-center chart review who underwent from January 2009 December 2023. Branch PAs were measured in systole, at narrowest point if focal stenosis was present. For diameter analyses, smaller used. Univariate Cox proportional hazards regression analysis...

10.1177/21501351251314381 article EN World Journal for Pediatric and Congenital Heart Surgery 2025-02-21

Abstract We report on 11 cases of amyoplasia in one identical twins. In total, 135 patients with were ascertained from a study 350 multiple congenital joint contractures (arthrogryposis). These twins represent 8% our amyoplasia. At least 18 sets have been reported previously. However, only four these appear to involve discordant for Thus, 15 which are affected identified.

10.1002/ajmg.1320150408 article EN American Journal of Medical Genetics 1983-08-01

Mesenchymal stem cells (MSCs) may improve myocardial function after I/R injury via paracrine effects, including the release of growth factors. Genetic modification MSCs is an appealing method to enhance MSC action. Ablation TNF receptor 1 (TNFR1), but not TNFR2, increases factor production. In this study, therefore, we hypothesized that 1) preischemic infusion derived from TNFR1 knockout (TNFR1KO) mice will further functional recovery and 2) TNFR2KO TNFR1/2KO abolish MSC-mediated protection...

10.1097/shk.0b013e3181cc0913 article EN Shock 2010-03-23

Background Bone marrow-derived mesenchymal stem cells (MSC) improve myocardial recovery after ischemia/reperfusion (I/R) injury. These effects are mediated in part by the paracrine secretion of angiogenic and tissue growth-promoting factors. Toll-like receptor 4 (TLR4) is expressed MSC induces apoptosis inhibits proliferation neuronal progenitors as well many other cell types. It unknown whether knock-out (KO) TLR4 will change properties turn MSC-associated protection. Methodology/Principal...

10.1371/journal.pone.0014206 article EN cc-by PLoS ONE 2010-12-03

Toll-like receptor 2 (TLR2), a key component of the innate immune system, is linked to inflammation and myocardial dysfunction after ischemia-reperfusion injury (I/R). Treatment heart with mesenchymal stem cells (MSCs) known improve recovery I/R in part by paracrine factors such as VEGF. However, it unknown whether TLR2 activation on MSCs affects MSC-mediated VEGF production. We hypothesized that knockout (TLR2KO MSCs) would 1) 2) increase MSC release. With isolated perfusion Sprague-Dawley...

10.1152/ajpheart.01087.2009 article EN AJP Heart and Circulatory Physiology 2010-02-20
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