4.5 Article

Direct Observation of Tunneling Nanotubes within Human Mesenchymal Stem Cell Spheroids

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 122, Issue 43, Pages 9920-9926

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.8b07305

Keywords

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Funding

  1. National Institutes of Health [R01 DE025475, R21 ES025350]
  2. Gordon and Betty Moore Foundation
  3. National Science Foundation Graduate Research Fellowship [1650042]
  4. UCD-LLNL Joint Graduate Mentorship Award
  5. NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH [R01DE025475] Funding Source: NIH RePORTER

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Tunneling nanotubes (TNTs) play an important role in cell-cell communication. TNTs have been predominantly reported among cells in monolayer culture. Using various imaging modalities, including scanning electron microscopy (SEM) and laser scanning confocal microscopy (LSCM), this work reports the finding of TNTs between cells within human mesenchymal stem cell (MSC) spheroids. TNTs visualized by SEM are consistent in size and geometry with those observed in cellular monolayer culture. LSCM imaging of living spheroids confirms the presence of F-actin filaments within the TNTs, which are known to maintain nanotube integrity. In addition, LSCM revealed the distribution of F-actin fibers across the entire spheroid body instead of being confined within individual cells. Intracellular material transport by TNTs was tested in MSC spheroids treated with cytochalasin D (CytoD), a known actin polymerization inhibitor for disrupting TNT formation. CytoD treatment decreased the transport of cytosolic material by at least four-fold compared to untreated spheroids. To the best of our knowledge, this work represents the first direct observation of TNTs within MSC spheroids. These findings offer new physical insight into cellular interactions within spheroids, providing structural information for increasing interests in spheroid-based cell therapy.

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