Cross-talk of healthy and impaired human tissues for dissection of disease pathogenesis

Alice Zoso1,2, Alessandro Zambon1,2, Onelia Gagliano1,2

  • 1Venetian Inst. of Molecular Medicine, Via Orus 2, Padova, 35129, Italy.

Biotechnology Progress
|December 15, 2018
PubMed

Insights

This study developed an in vitro model to investigate how diseased adipose tissue affects skeletal muscle. The model revealed that obese adipose tissue disrupts healthy muscle insulin sensitivity, mimicking early diabetes development.

Area of Science:

  • Biotechnology
  • Tissue Engineering
  • Metabolic Disease Research

Background:

  • Systemic diseases involve complex tissue interactions challenging to study in vivo.
  • In vitro models offer control but struggle to replicate systemic human responses.
  • Obesity is a major risk factor for type 2 diabetes mellitus, highlighting the need to understand adipose-muscle crosstalk.

Purpose of the Study:

  • To develop an in vitro model simulating systemic interactions between adipose and skeletal muscle tissues.
  • To investigate the impact of diseased adipose tissue on healthy skeletal muscle function.
  • To understand early-stage type 2 diabetes mellitus pathogenesis through tissue crosstalk.

Main Methods:

  • Established a 3D ex vivo culture of human adipose tissue from an obese donor.
  • Created a human skeletal muscle-on-chip model using primary cells and topological cues.
  • Stimulated the muscle-on-chip with conditioned medium from the adipose tissue culture.

Main Results:

  • The skeletal muscle-on-chip model successfully mimicked in vivo responses.
  • Conditioned medium from obese adipose tissue impaired insulin sensitivity in healthy skeletal muscle.
  • This impairment reflects early-stage changes observed in type 2 diabetes.

Conclusions:

  • The developed in vitro system effectively models human tissue crosstalk relevant to metabolic diseases.
  • This platform facilitates the study of systemic interactions between unhealthy and healthy tissues.
  • The findings provide insights into early type 2 diabetes pathogenesis via adipose-muscle signaling.

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