Alvin Jogasuria

ORCID: 0000-0002-8569-339X
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About
Contact & Profiles
Research Areas
  • Alcohol Consumption and Health Effects
  • Hematopoietic Stem Cell Transplantation
  • Liver Disease Diagnosis and Treatment
  • Lipid metabolism and biosynthesis
  • Fibroblast Growth Factor Research
  • Clinical Nutrition and Gastroenterology
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Epigenetics and DNA Methylation
  • Lung Cancer Treatments and Mutations
  • RNA modifications and cancer
  • T-cell and B-cell Immunology
  • Metabolism and Genetic Disorders
  • Blood disorders and treatments
  • Immune Cell Function and Interaction
  • Cancer-related molecular mechanisms research
  • Immune Response and Inflammation
  • Organ Transplantation Techniques and Outcomes
  • NF-κB Signaling Pathways
  • MicroRNA in disease regulation
  • Eicosanoids and Hypertension Pharmacology
  • Neutropenia and Cancer Infections
  • Medical Imaging and Pathology Studies
  • Kruppel-like factors research
  • Lipid metabolism and disorders
  • Adipose Tissue and Metabolism

Case Western Reserve University
2019-2022

Northeast Ohio Medical University
2015-2019

Pharmaceutical Biotechnology (Czechia)
2017

Zhuhai Hospital of Integrated Traditional Chinese and Western Medicine
2017

Shanghai University of Traditional Chinese Medicine
2017

Matrix Research (United States)
2016

Lipin-1 is a Mg2+-dependent phosphatidic acid phosphohydrolase involved in the generation of diacylglycerol during synthesis phospholipids and triglycerides. Ethanol-mediated inhibitory effects on adipose-specific lipin-1 expression were associated with experimental steatohepatitis rodents. In present study, using an overexpression transgenic (Lpin1-Tg) mouse model, we tested hypothesis that mice might dampen ethanol-induced liver damage. Experimental alcoholic was induced by pair-feeding...

10.1002/hep4.1333 article EN cc-by-nc-nd Hepatology Communications 2019-03-12

Ethanol-mediated injury, combined with gut-derived lipopolysaccharide (LPS), provokes generation of proinflammatory cytokines in Kupffer cells, causing hepatic inflammation. Among the mediators these effects, miR-217 aggravates ethanol-induced steatosis hepatocytes. However, role liver inflammation process is unknown. Here, we examined responses to ethanol, LPS, or a combination ethanol and LPS RAW 264.7 macrophages primary cells. In macrophages, substantially exacerbated LPS-mediated...

10.1016/j.ajpath.2015.01.030 article EN cc-by-nc-nd American Journal Of Pathology 2015-03-29

MitoNEET (mNT) (CDGSH iron-sulfur domain-containing protein 1 or CISD1) is an outer mitochondrial membrane that donates 2Fe-2S clusters to apo-acceptor proteins. In the present study, using a global mNT knock-out (mNTKO) mouse model, we investigated in vivo functional role of development alcoholic steatohepatitis. Experimental steatohepatitis was achieved by pair feeding wild-type (WT) and mNTKO mice with Lieber-DeCarli ethanol-containing diets for 4 weeks. Strikingly, chronically...

10.1074/jbc.m116.737015 article EN cc-by Journal of Biological Chemistry 2016-08-30

Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive disease characterized by interstitial remodeling and dysfunction. The etiology of IPF not completely understood but involves pathologic inflammation subsequent failure to resolve in response epithelial injury. Treatments for are limited anti-inflammatory immunomodulatory agents, which only partially effective. Prostaglandin E2 (PGE2) disrupts TGFβ signaling suppresses myofibroblast differentiation, however practical strategies...

10.1038/s41598-020-68336-0 article EN cc-by Scientific Reports 2020-07-15

Abstract Lipin-1 is a phosphatidate phosphohydrolase (PAP) required for the generation of diacylglycerol during glycerolipid synthesis, and exhibits dual functions in regulation lipid metabolism. has been implicated pathogenesis alcoholic liver disease (ALD). In present study, we assessed lipin-1 function myeloid cells ALD using cell-specific knockout (mLipin-1KO) mouse model. Utilizing Gao-binge ethanol feeding protocol, matched mLipin-1KO mice littermate loxP control (WT) were pair-fed...

10.1038/srep34117 article EN cc-by Scientific Reports 2016-09-26

The splenic microenvironment regulates hematopoietic stem and progenitor cell (HSPC) function, particularly during demand-adapted hematopoiesis; however, practical strategies to enhance support of transplanted HSPCs have proved elusive. We previously demonstrated that inhibiting 15-hydroxyprostaglandin dehydrogenase (15-PGDH), using the small molecule (+)SW033291 (PGDHi), increases BM prostaglandin E2 (PGE2) levels, expands HSPC numbers, accelerates hematologic reconstitution after...

10.1172/jci.insight.143658 article EN cc-by JCI Insight 2021-02-28

Aplastic anemia (AA) is a human immune-mediated bone marrow failure syndrome that treated by stem cell transplantation for patients who have matched related donor and immunosuppressive therapy (IST) those do not. Responses to IST are variable, with still at risk prolonged neutropenia, transfusion dependence, immune suppression, severe opportunistic infections. Therefore, additional therapies needed accelerate hematologic recovery in receiving front-line IST. We shown inhibiting...

10.1016/j.bbmt.2020.04.010 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2020-05-15

Emerging evidence implicates the eicosanoid molecule prostaglandin E2 (PGE2) in conferring a regenerative phenotype to multiple organ systems following tissue injury. As aging is part characterized by loss of stem cells’ capacity, we tested hypothesis that prostaglandin-degrading enzyme 15-hydroxyprostaglandin dehydrogenase (15-PGDH) contributes diminished fitness aged mice. Here demonstrate genetic 15-PGDH ( Hpgd ) confers protective effect on murine hematopoietic and gastrointestinal (GI)...

10.1371/journal.pone.0268787 article EN cc-by PLoS ONE 2022-05-19

Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive disease characterized by interstitial remodeling and dysfunction. The etiology of IPF not completely understood but involves pathologic inflammation subsequent failure to resolve in response epithelial injury. Therapeutic strategies for are limited anti-inflammatory immunomodulatory agents, which only partially effective. Prostaglandin E2 (PGE2) disrupts TGFβ signaling suppresses myofibroblast differentiation, however practical...

10.1101/2019.12.16.878215 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2019-12-18

Aplastic anemia (AA) is a human immune mediated bone-marrow failure syndrome that treated by stem cell transplantation for patients who have matched related donor or immunosuppressive therapy (IST) those do not. Responses to IST are variable, with still at risk prolonged neutropenia, transfusion-dependence, suppression, and severe opportunistic infections. Therefore, additional therapies accelerate hematologic recovery in receiving front line needed. We shown inhibiting...

10.1101/2020.04.07.030312 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-04-09

Abstract The splenic microenvironment regulates hematopoietic stem and progenitor cell (HSPC) function, particularly during demand-adapted hematopoiesis, however practical strategies to enhance support of transplanted HSPCs have proven elusive. We previously demonstrated that inhibiting 15-hydroxyprostaglandin dehydrogenase (15-PGDH), using the small molecule (+)SW033291 (PGDHi), increases bone marrow (BM) prostaglandin E2 (PGE2) levels, expands HSPC numbers, accelerates hematologic...

10.1101/2020.09.17.302422 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-09-18
David A. Dorward Christopher D. Lucas Gavin Chapman Christopher Haslett Kevin Dhaliwal and 95 more Adriano G. Rossi Sameh Mikhail Christopher Albanese Michael J. Pishvaian Sandhya Xavier Sara F. Rinaldi Sofia Makieva Lorraine Frew Jean Wade Adrian Thomson Carmel M. Moran Jane E. Norman Sarah J. Stock Ola Z. Ismail Xizhong Zhang Junjun Wei Aaron Haig Bradley M. Denker Rita S. Suri Alp Şener Lakshman Gunaratnam Satu Lehti Peter Sjövall Reijo Käkelä Mikko I. Mäyränpää Petri T. Kovanen Katariina Öörni Ming Liang Lauren E. Woodard Anlin Liang Jinlong Luo Matthew W. Wilson William A. Mitch Jizhong Cheng Andréia Z. Chignalia Stephen J. Vogel Albert B. Reynolds Dolly Mehta Randal O. Dull Richard D. Minshall Asrar B. Malik Yuru Liu Ruth J. Pepper Hsu-Han Wang Gayathri Rajakaruna Eugenia Papakrivopoulou Thomas Vogl Charles D. Pusey H Cook Alan D. Salama Yuji Ishida Chihiro Yamasaki Ami Yanagi Yasumi Yoshizane Kazuyuki Fujikawa Koichi Watashi Hiromi Abe Takaji Wakita C. Nelson Hayes Kazuaki Chayama Chise Tateno Huquan Yin Xiaomei Liang Alvin Jogasuria Nicholas O. Davidson Min You Daniel Delitto Kien Pham Adrian C. Vlada George A. Sarosi Ryan Thomas K.E. Behrns Chen Liu Steven G. Hughes Shannon M. Wallet José G. Treviño Hideya Kawasaki Isao Kosugi Makiko Sakao‐Suzuki Shiori Meguro Yoshifumi Arai Yoshihiro Tsutsui Toshihide Iwashita Peter Gardner Samia Yazid Colin J. Chu David A. Copland Peter Adamson Andrew W. Dick Virginia L. Calder Monika Siwetz Martina Dieber‐Rotheneder M Cervar-Zivkovic Daniel Kummer Julia Kremshofer

10.1016/s0002-9440(15)00158-3 article EN publisher-specific-oa American Journal Of Pathology 2015-04-20

Elevated triglycerides (TGs) are an independent risk factor for cardiovascular disease (CVD). Lipoprotein lipase (LPL) found along the capillary endothelium catalyzes hydrolysis of TG rich lipoproteins and chylomicrons. Angiopoietin-like (ANGPTL) proteins including ANGPTL3 have been identified as endogenous inhibitors LPL. As a result, overexpression is associated with elevated TGs increased CVD. Excessive alcohol intake secondary hypertriglyceridemia may worsen seen in primary lipid...

10.1096/fasebj.29.1_supplement.885.21 article EN The FASEB Journal 2015-04-01

ABSTRACT Emerging evidence implicates the eicosanoid molecule prostaglandin E2 (PGE2) in conferring a regenerative phenotype to multiple organ systems following tissue injury. As aging is part characterized by loss of stem cells’ capacity, we tested hypothesis that prostaglandin-degrading enzyme 15-hydroxyprostaglandin dehydrogenase (15-PGDH) contributes diminished fitness aged mice. Here demonstrate genetic 15-PGDH ( Hpgd ) confers protective effect on murine hematopoietic and...

10.1101/2020.12.22.424017 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-12-22
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