2016
DOI: 10.1016/j.acthis.2016.06.001
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Ultrastructural and immunohistochemical characteristics of telocytes in the skin and skeletal muscle of newborn rats

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Cited by 13 publications
(15 citation statements)
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References 57 publications
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“…In the present study we have described for the first time the distribution of TCs in murine skeletal muscles damaged by forced EC and provided novel experimental evidence supporting their morpho-functional interaction with activated SCs. In particular, confocal immunofluorescence analysis of intact control muscle sections revealed the presence of CD34 + CD31 − elongated, thin and varicose processes organized in an interstitial network alongside the striated myofibers and around blood vessels, consistent with the previous description of telopodes of TCs in the endomysial and perimysial sheaths of skeletal muscle 10,1315,17 . Notably, in EC-damaged muscles this CD34 + CD31 − telopode network appeared particularly extended and was preferentially arranged around activated SCs that displayed Pax7 and MyoD nuclear positivity and were located in their distinctive site at the periphery of striated myofibers.…”
Section: Discussionsupporting
confidence: 88%
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“…In the present study we have described for the first time the distribution of TCs in murine skeletal muscles damaged by forced EC and provided novel experimental evidence supporting their morpho-functional interaction with activated SCs. In particular, confocal immunofluorescence analysis of intact control muscle sections revealed the presence of CD34 + CD31 − elongated, thin and varicose processes organized in an interstitial network alongside the striated myofibers and around blood vessels, consistent with the previous description of telopodes of TCs in the endomysial and perimysial sheaths of skeletal muscle 10,1315,17 . Notably, in EC-damaged muscles this CD34 + CD31 − telopode network appeared particularly extended and was preferentially arranged around activated SCs that displayed Pax7 and MyoD nuclear positivity and were located in their distinctive site at the periphery of striated myofibers.…”
Section: Discussionsupporting
confidence: 88%
“…Only recently, TCs entered this scenario as a new distinctive type of interstitial cells that may potentially behave as nursing cells for SC-mediated skeletal muscle regeneration. However, it must be frankly recognized that such supporting role for TCs has only been supposed on the basis of their in situ identification in the close vicinity of SCs in healthy skeletal muscles 10,1315,17 , their possible role during early myogenesis 28 , and their well-documented interaction and/or cross-talk with stem/progenitor cells in other organs 3,10,2934 . Indeed, at present, the effective occurrence of a morpho-functional interplay between TCs and SCs in injured skeletal muscles has yet to be demonstrated with certainty.…”
Section: Discussionmentioning
confidence: 99%
“…We also observed that the peritubular CD34-negative/α-SMA-positive myoid cells/myofibroblasts coexpress PDGFRα, which further strengthen the evidence that single immunohistochemistry is not enough and can lead to misleading results when studying TCs by light microscopy. Since the expression of the stemness-related marker c-kit/CD117 has been reported in TCs from some tissues and organs, such as in the heart, skeletal muscles and female reproductive system 6 , 7 , 12 , 14 , 16 , 59 , we also double immunolabeled our human testicular sections for CD34/c-kit. Hence, we found that human testicular TCs are c-kit/CD117-negative, as previously documented in other human organs including the gastrointestinal tract and the skin 36 , 52 .…”
Section: Discussionmentioning
confidence: 99%
“…In addition, several tumors can have their origin in CD34+SCs/TCs [ 32 , 33 , 34 ]. In the skin, the suggested roles of CD34+SCs/TCs include mechanical support, regeneration (tandem between TCs and stem cells), communication (intercellular contacts and extracellular vesicles) and endocytosis, immune regulation, modulation of fibroblasts, mast cells and macrophages, reduction of inflammatory response, participation in metabolism, homeostasis, (neo) angiogenesis and in the interaction between collagen and elastic fibers [ 3 , 4 , 13 , 14 , 15 , 18 , 22 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 ].…”
Section: Introductionmentioning
confidence: 99%