PIPages
Labs

Michinari Nakamura

Rutgers University-New Brunswick, NJ·Physiology

Obesity can damage the heart directly, apart from high blood pressure, diabetes or clogged arteries. This condition, obesity cardiomyopathy, thickens and stiffens the heart and can lead to heart failure.

Fields

Physiology

Medicine & Clinical Research

Microbiology & Immunology

Topics

obesity cardiomyopathy

heart failure with preserved ejection fraction

HFpEF

Grants
1 known grant, through Apr 2030

What they work on

  1. Determine whether increased Bcl-xS, a short form of the Bcl2l1 protein, in the spleen protects against heart inflammation and obesity cardiomyopathy, using Bcl-xS knockout mice on a high-fat diet.
  2. Test how asparagine metabolism in B cells contributes to cardiomyopathy after a high-fat diet or Bcl-xS deletion, using stable-isotope labeling metabolomics and engineered mice.
  3. Uncover how Bcl-xS suppresses asparagine metabolism in B cells, using proteomics and adeno-associated virus gene delivery.

More about the research

The heart starts burning fat in an uncontrolled way, and the excess fat becomes toxic, a process called lipotoxicity. Because obesity affects the whole body, this project asks whether fat-induced changes in a distant organ, the spleen, help drive heart disease.

Why it matters

Obesity is a leading driver of heart disease and death, and there are few targeted treatments for heart damage caused by obesity itself. By linking the spleen's immune cells to heart inflammation, this work could reveal a new drug target, such as B-cell asparagine metabolism or Bcl2l1 splicing, for preventing or reversing obesity cardiomyopathy.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Role of Lipotoxicity-Induced Splenic Cell Alternative Splicing in Obesity Cardiomyopathy

NIH · Aug 2026 – Apr 2030

Closest labs

Tammy Kindel

Medical College of Wisconsin, WI·Medicine & Clinical Research

Test whether the gut microbiome after sleeve gastrectomy raises blood bile acids that activate FXR, a bile-acid sensor, using fecal transfer from operated mice and metagenomic sequencing of rodent and human stool.

Stefano Morotti

University of California-Davis, CA·Physiology

Identify key molecular and cellular changes in excitation-contraction coupling, the link between electrical signals and heartbeats, in a mouse model of heart failure with preserved ejection fraction (HFpEF), using functional and transcriptomic data.

Thomas Vondriska

University of California-Los Angeles, CA·Physiology

Map gene activity, chromatin accessibility and histone modifications in heart, kidney and liver of ZSF1 rats as HFpEF develops, building the first multi-organ epigenomic atlases of the disease.

The school

Rutgers University-New Brunswick: 57 labs on PI Pages, $837M a year on research, 713 research doctorates a year.

More about Rutgers University-New Brunswick

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