Specialist article | PRP research | Cell communication

Telocytes and PRP: current research on possible cell interactions

Telocytes are described in tissue research as stromal cells with long cellular extensions. PRP contains platelet-derived mediators that may be involved in physiological repair and remodelling processes. Whether telocytes clinically mediate PRP signals in humans is not currently established.

In brief

This article describes biological and preclinical research approaches relating to telocytes and platelet-rich plasma. The mechanisms discussed are mainly based on experimental, histological and preclinical data. They do not allow conclusions on clinical efficacy, treatment recommendations or standardised therapeutic protocols.

What are telocytes?

Telocytes are interstitial cells with a small cell body and long, very thin extensions called telopodes. These structures can extend over comparatively long distances in tissue and establish contact with different cell types.

They have been described in skin, heart, lung, liver, digestive tract, joint-related tissues and other organs. They are often found close to blood vessels, nerve fibres or stromal cell niches.

Described

Telocytes have been detected in different tissues and characterised morphologically.

Discussed

Their potential role in stromal organisation, cell communication and tissue remodelling is being investigated.

Not established

A clinically usable telocyte mechanism in connection with PRP has not been proven.

Distinction from fibroblasts

Telocytes are not simply unusually long fibroblasts. Morphologically, they differ by their small cell body and long, thin processes with alternating dilations, mainly described by electron microscopy. There is no single marker that clearly defines telocytes for routine use.

Evidence classification

Identification usually requires a combination of ultrastructure, cell morphology, tissue location and marker profile. This is currently not suitable for routine clinical diagnostics.

PRP: biological basics

Platelet-rich plasma, or PRP, is plasma obtained from autologous blood with an increased platelet concentration. Venous blood is collected, anticoagulated and centrifuged. Depending on the system and protocol, different fractions are produced and the platelet-rich portion is collected.

PRP contains platelets and platelet-derived mediators, including growth factors and cytokines that can be involved in physiological repair and remodelling processes. The exact composition is not uniform.

Influencing factors include blood volume, anticoagulant, tube type, centrifugation parameters, RCF/g-force, spin time, leukocyte content, activation and time between preparation and use.

Evidence classification

PRP is not a single standardised preparation. Any efficacy statement must be assessed by indication and methodology. Studies are only meaningfully comparable when the preparation method is documented transparently.

Possible interactions between telocytes and PRP mediators

Research is examining whether telocytes can respond to mediators contained in PRP, especially signalling molecules released by platelets after activation. These are mechanistic hypotheses, not proof of clinical effect.

Receptors and signalling pathways

Receptor axes have been described for telocytes that could in principle interact with PRP-associated mediators, including PDGF-, TGF-β- and VEGF-related pathways. Such mechanisms are biologically plausible, but they do not prove clinical relevance.

Cell contacts and vesicles

Telocytes form contacts with other cell types and can release extracellular vesicles containing proteins, microRNAs and other signalling molecules. PRP also contains vesicular components. Mutual influence is experimentally conceivable; its clinical relevance is not clarified.

Important distinction

Telocytes should not currently be presented as an established mechanism of PRP. The appropriate wording is: possible involvement in stromal cell communication, mainly studied preclinically, not clinically proven.

Preclinical and histological research fields

Several studies examine telocytes in tissues involved in remodelling and repair. The following examples are for scientific classification only. They do not describe established treatment areas and are not treatment recommendations.

Skin models and stromal repair zones

In preclinical and histological work, telocytes have been described in healing skin areas, sometimes near newly formed microvessels and stromal repair zones. A 2024 publication discusses telocytes as possible participants in PRP-associated cellular processes in skin tissue. These observations do not prove a clinical PRP treatment effect.

Myocardial and joint-related tissue research

In the myocardium, telocytes are investigated as part of the stromal network. In joint-related tissues, such as synovial membrane, their specific role remains a research question. Clinical PRP studies in orthopaedic questions are heterogeneous and do not prove a direct telocyte-mediated effect.

Why the evidence is limited

There is no single marker that reliably detects telocytes in routine practice. Electron microscopy, morphology and marker panels are often required, which limits comparability and reproducibility.

Cell culture, animal and tissue studies can describe biological mechanisms. They do not automatically show that a procedure is clinically effective, safe or superior in humans. Correlation is not causality: the observation of telocytes in tissue remodelling does not prove that they control the process.

Why PRP studies are difficult to compare

Preparation

  • Single-spin or double-spin
  • RCF/g-force and spin time
  • Tube type and anticoagulant

Composition

  • Leukocyte-poor or leukocyte-rich
  • Platelet concentration
  • Final volume and fraction

Documentation

  • System and IFU
  • LOT/batch of materials
  • Timing of use

Practical classification for professional users

PRP should not be explained or promoted through telocyte-related efficacy claims. A clean, documented and indication-specific approach within the relevant legal, hygienic and product-specific requirements is more appropriate.

  • document the PRP system and instructions for use
  • record blood volume, anticoagulant and single-use materials
  • use RCF/g-force rather than RPM alone
  • document spin duration, final volume and fraction
  • record LOT/batch of materials
  • document information, consent and follow-up

No telocyte-derived protocols

Current evidence does not allow standardised protocols for targeted telocyte activation by PRP. Professional users should follow the IFU, hygiene requirements, internal SOPs and individual professional judgement.

Safety, information and limits

PRP applications belong in trained hands and must be performed according to the relevant system specifications. Possible local reactions include pain, swelling, redness or bruising at the application site. Infections are rare but possible with improper handling. These notes do not replace medical evaluation or product-specific instructions for use.

FAQ: telocytes and PRP

Is there a clinically proven synergy between telocytes and PRP?

No. There are preclinical and histological indications of possible interactions. A clinically established telocyte-PRP synergy has not been proven.

Are telocytes the mechanism of action of PRP?

This is not established. Telocytes are being investigated as part of stromal cell communication, but they do not currently explain a clinical PRP effect.

Can PRP be used specifically to activate telocytes?

There is currently no standardised, clinically validated procedure for this. Telocyte-related PRP protocols cannot be derived from the current evidence.

Why are PRP studies difficult to compare?

PRP differs according to preparation, leukocyte content, activation, centrifugation, tube type and system used. Studies and applications therefore need precise documentation.

Conclusion

Telocytes are an interesting topic in current tissue research. A possible interaction with PRP mediators is biologically plausible, but the current evidence is not sufficient to derive established clinical mechanisms, treatment recommendations or standardised protocols. Communication should clearly distinguish between preclinical hypotheses, histological observations and clinically established evidence.

Literature and further reading

  1. Manole CG et al. Skin Telocytes Could Fundament the Cellular Mechanisms of Wound Healing in Platelet-Rich Plasma Administration. Cells. 2024.
  2. Manetti M et al. Telocytes in regenerative medicine. Journal of Cellular and Molecular Medicine. 2019.
  3. Cretoiu D et al. Telocytes and their extracellular vesicles — evidence and hypotheses. International Journal of Molecular Sciences. 2019.
  4. Cismașiu VB, Popescu LM. Telocytes transfer extracellular vesicles loaded with microRNAs to stem cells. Journal of Cellular and Molecular Medicine. 2015.
  5. Klein M et al. Cardiac Telocytes 16 Years on — What Have We Learned So Far? International Journal of Molecular Sciences. 2021.
  6. Zheng Y et al. Intramyocardial transplantation of cardiac telocytes decreases myocardial infarction and improves post-infarcted cardiac function in rats. Journal of Cellular and Molecular Medicine. 2014.
Product added to wishlist
Product added to compare.
group_work Cookie consent