Skip to main content

Advertisement

Log in

Disease-related biomarkers as experimental endpoints in 3D skin culture models

  • Review
  • Published:
Cytotechnology Aims and scope Submit manuscript

Abstract

The success of in vitro 3D models in either recapitulating the normal tissue physiology or altered physiology or disease condition depends upon the identification and/or quantification of relevant biomarkers that confirm the functionality of these models. Various skin disorders, such as psoriasis, photoaging, vitiligo, etc., and cancers like squamous cell carcinoma and melanoma, etc. have been replicated via organotypic models. The disease biomarkers expressed by such cell cultures are quantified and compared with the biomarkers expressed in cultures depicting the normal tissue physiology, to identify the most prominent variations in their expression. This may also indicate the stage or reversal of these conditions upon treatment with relevant therapeutics. This review article presents an overview of the important biomarkers that have been identified in in-vitro 3D models of skin diseases as endpoints for validating the functionality of these models.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Adapted from Cario-André et al. 2018 (Cario-André et al. 2018)

Fig. 2

(Adapted from Alsharabasy A et al., 2021; under CC BY 4.0) (Alsharabasy and Pandit 2021)

Fig. 3

Similar content being viewed by others

Data availability

Data sharing not applicable to this article as no datasets were generated or analysed during the current review article.

Abbreviations

FLG:

Filaggrin

LOR:

Loricrin

CA2:

Carbonic anhydrase 2

NELL2:

Neural epidermal growth factor like2

IHC:

Immunohistochemical staining

TSLP:

Thymic stromal lymphopoeitin

RHPE:

Reconstructed human pigmented epidermis

TGFβ:

Transforming growth factor β

MCP-1:

Monocyte chemo-attractant protein

SPARC:

Secreted protein acidic and rich in cysteine

LESA MS:

Liquid extraction surface analysis MS

H and E:

Haematoxylin and Eosin staining

PAS:

Periodic acid-Schiff staining

COL1A1:

Collagen type I A1

COL7A1:

Collagen type VII A1

CCND1:

Cyclin D1

DCN:

Decorin

ELN:

Elastin

FBN1:

Fibrillin 1

GPX1:

Glutathione peroxidase 1

GSR:

Glutathione reductase

IL1α:

Interleukin 1α

IL10:

Interleukin 10

ITGβ1:

Integrin β1

IVL:

Involucrin

MMP1:

Matrix metalloproteinase 1

MMP9:

Matrix metalloproteinase-9

CPDs:

Cyclopyrimidine dimers

4-HNE:

4-Hydroxynonenal

GmCSF:

Granulocyte macrophage colony-stimulating factor

α-SMA:

Alpha smooth muscle actin

ECML:

Extra Cellular Matrix

FFAs:

Free Fatty Acids

SCC:

Squamous Cell Carcinoma

MMPs:

Matrix Metalloproteinases

DEJ:

Dermal Epidermal Junction

IL:

Interleukin

TNF:

Tumor Necrosis Factor

IFN:

Interferon

MGP:

Matrix Gla Protein

VEFG:

Vascular endothelial growth factor

MCP:

Monocyte chemoattractant protein

CPD:

Cyclo-pyrimidine dimers

DP:

Dermal Papilla

ALP:

Alkaline Phosphatase

NCAM:

Neural cell adhesion molecule

SMA:

Smooth Muscle antibody

BMP:

Bone morphogenetic protein

PAS:

Periodic acid-Schiff

MTT:

3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium Bromide

C/EBPβ:

C/CAAT-enhancer-binding proteins

References

Download references

Acknowledgements

Corresponding authors, R.J. and P.D. are thankful to Department of Biotechnology (DBT-ATGC) and Department of Science and Technology (DST-PURSE), Government of India for providing financial support.

Funding

D.C. is financially supported by Department of Biotechnology (DBT-ATGC) and Department of Science and Technology (DST-PURSE), Government of India.

Author information

Authors and Affiliations

Authors

Contributions

Literature survey, data analysis, study design, writing—draft preparation: DC, SP; Supervision: PD, RJ; Writing—reviewing and editing: PD.

Corresponding authors

Correspondence to Ratnesh Jain or Prajakta Dandekar.

Ethics declarations

Conflict of interests

The authors have no relevant financial and non-financial interests to disclose.

Ethical Approval

"Not Applicable".

Informed consent

"Not Applicable".

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (PDF 203 KB)

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chaturvedi, D., Paranjape, S., Jain, R. et al. Disease-related biomarkers as experimental endpoints in 3D skin culture models. Cytotechnology 75, 165–193 (2023). https://doi.org/10.1007/s10616-023-00574-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10616-023-00574-2

Keywords

Navigation