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Telocytes: current methods of research, challenges and future perspectives

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Abstract

Telocytes (TCs) are CD34-positive interstitial cells that have long cytoplasmic projections, called telopodes; they have been identified in several organs and in various species. These cells establish a complex communication network between different stromal and epithelial cell types, and there is growing evidence that they play a key role in physiology and pathology. In many tissues, TC network impairment has been implicated in the onset and progression of pathological conditions, which makes the study of TCs of great interest for the development of novel therapies. In this review, we summarise the main methods involved in the characterisation of these cells as well as their inherent difficulties and then discuss the functional assays that are used to uncover the role of TCs in normal and pathological conditions, from the most traditional to the most recent. Furthermore, we provide future perspectives in the study of TCs, especially regarding the establishment of more precise markers, commercial lineages and means for drug delivery and genetic editing that directly target TCs.

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Abbreviations

ApoE:

Apolipoprotein E

BMP4:

Bone morphogenetic protein 4

CAVD:

Calcific aortic valve disease

CD31:

Cluster of differentiation 31

CD34:

Cluster of differentiation 34

CD81:

Cluster of differentiation 81

CD90:

Cluster of differentiation 90

Cdip1:

Cell death inducing p53 target 1

CREB1:

CAMP response element binding protein 1

CRISPR-Cas9:

Clustered regularly interspaced short palindromic repeats–CRISPR associated protein 9

CSCs:

Cardiac stem cells

CTGF:

Connective tissue growth factor

Dkk3:

Dickkopf-related protein 3

DUOX2:

Dual oxidase 2

ECM:

Extracellular matrix

EGF:

Epidermal growth factor

EVs:

Extracellular vesicles

Foxl1:

Forkhead box L1

HCC:

Hepatocellular carcinoma

HGF:

Hepatocyte growth factor

IL-6:

Interleukin 6

lncRNA:

Long noncoding RNA

LPS:

Lipopolysaccharide

MCP-1:

Monocyte chemoattractant protein-1

MHY14:

Myosin heavy chain 14

MIP-1α:

Macrophage inflammatory protein 1α

MIP-2:

Macrophage inflammatory protein-2

miR-146a-5p:

MicroRNA 146a-5p

miRNA-21-5p:

MicroRNA 21-5p

miR-942-3p:

MicroRNA 942-3p

MMP9:

Matrix metalloproteinase 9

MSCs:

Mesenchymal stem cells

MYL9:

Myosin regulatory light polypeptide 9

MyoD:

Myoblast determination protein 1

Pax7:

Paired box protein 7

PDGFβ:

Platelet-derived growth factor subunit β

PDGFRα:

Platelet-derived growth factor receptor α

PDGFRβ:

Platelet-derived growth factor receptor β

qPCR:

Quantitative polymerase chain reaction

Rosa-mTmG:

ROSA26-membrane-tdT-membrane-EGFP

scRNA-seq:

Single-cell RNA sequencing

SDF-1:

Stromal cell-derived factor 1

SEM:

Scanning electron microscopy

sFRP1:

Secreted Frizzled-related protein 1

SNHG16:

Small nucleolar RNA host gene 16

SPRR1A:

Small proline-rich repeat protein 1A

TAGLN:

Transgelin

TC:

Telocyte

TEM:

Transmission electron microscopy

TGFβ1:

Transforming growth factor β1

TP:

Telopode

VEGF:

Vascular endothelial growth factor

Wnt:

Wingless-related integration site

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Acknowledgements

We thank FAPESP and CNPq for the funding and the researchers of the School of Chemical Engineering, University of Birmingham, as well as of INFABIC lab at the State University of Campinas (UNICAMP).

Funding

This work was supported by FAPESP (São Paulo Research Foundation) (contract number 2021/02303-7 (to HFC)) and CNPq (Brazilian National Council for Scientific and Technological Development) (contract numbers 465699/2014-6 (to HCF) and 104276/2023-1 (to BDAS)).

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Correspondence to Hernandes F. Carvalho.

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Sanches, B.D.A., Teófilo, F.B.S., Brunet, M.Y. et al. Telocytes: current methods of research, challenges and future perspectives. Cell Tissue Res 396, 141–155 (2024). https://doi.org/10.1007/s00441-024-03888-5

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