4.4 Article

Characterization of the structure, vascularity, and stem/progenitor cell populations in porcine Achilles tendon (PAT)

Journal

CELL AND TISSUE RESEARCH
Volume 384, Issue 2, Pages 367-387

Publisher

SPRINGER
DOI: 10.1007/s00441-020-03379-3

Keywords

Achilles tendon; Paratenon; Interfascicular matrix; Fascicles; Stem cells

Categories

Funding

  1. National Institutes of Health [AR061395, AR065949, AR070340]

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This study characterized the porcine Achilles tendon (PAT) in terms of its structural components, vascularity, and resident tendon cells. The findings revealed the presence of blood vessel-like tissues in the paratenon and IFM, with cells expressing characteristics of vascular stem/progenitor cells. The cells isolated from paratenon and IFM displayed the ability for multi-differentiation and expressed various markers associated with stem/progenitor cells. These findings contribute to a better understanding of the vascular and cellular mechanisms involved in tendon homeostasis, injury, healing, and regeneration.
This study aimed to characterize porcine Achilles tendon (PAT) in terms of its structural components, vascularity, and resident tendon cells. We found that PAT is composed of a paratenon sheath, a core of fascicles, and an endotenon/interfascicular matrix (IFM) that encases the fascicle bundles. We analyzed each of these three tendon components structurally using tissue sections and by isolating cells from each component and analyzing in vitro. Many blood vessel-like tissues were present in the paratenon and IFM but not in fascicles, and the vessels in the paratenon and IFM appeared to be inter-connected. Cells isolated from the paratenon and IFM displayed characteristics of vascular stem/progenitor cells expressing the markers CD105, CD31, with alpha-smooth muscle actin (alpha-SMA) localized surrounding blood vessels. The isolated cells from paratenon and IFM also harbored abundant stem/progenitor cells as evidenced by their ability to form colonies and express stem cell markers including CD73 and CD146. Furthermore, we demonstrate that both paratenon and IFM-isolated cells were capable of undergoing multi-differentiation. In addition, both paratenon and IFM cells expressed elastin, osteocalcin, tubulin polymerization promoting protein (TPPP), and collagen IV, whereas fascicle cells expressed none of these markers, except collagen I. The neurotransmitter substance P (SP) was also found in the paratenon and IFM-localized surrounding blood vessels. The findings of this study will help us to better understand the vascular and cellular mechanisms of tendon homeostasis, injury, healing, and regeneration.

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