Human Umbilical Cord Cells (Wharton's Jelly)

Cat.No.: CSC-C2860

Species: Human

Source: Umbilical Cord

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Cat.No.
CSC-C2860
Description
Wharton's jelly cells are derived from the inner jelly substance in the umbilical cord. Wharton's jelly cells are isolated from a single donor. These cells have characteristics of MSCs and are widely investigated for their use in therapeutic applications. These cells enable researchers to investigate stem cell properties, regenerative medicine, and tissue engineering. In addition, they may be used for developmental studies.
Development period: Postnatal
Species
Human
Source
Umbilical Cord
Disease
Normal
Storage and Shipping
Store at -196 °C (LN2) upon receipt until ready to culture.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Human Wharton's Jelly Mesenchymal Stem Cells (hWJ-MSCs) are derived from Wharton's Jelly, the gelatinous extracellular matrix found within the human umbilical cord. As fetal tissue obtained at birth, these perinatal stem cells have several advantages compared to adult-derived counterparts: they can be harvested non-invasively and without ethical concerns. Cells derived from this tissue are considered to be more primitive than adult-derived MSCs, giving them a higher proliferative ability along with lower immunogenicity and stronger secretome.

Similar to adult MSCs isolated from bone marrow and adipose tissue, hWJ-MSCs express mesenchymal markers (CD73, CD90, CD105) and lack expression of HLA class II, leading to low likelihood for rejection upon allogeneic transplantation. Numerous studies have shown that hWJ-MSCs possess powerful differentiation potential, particularly along chondrocytic and osteogenic lineages. Early studies into Wharton's Jelly focused on its ability to generate mesodermal tissue-types. However, the current literature highlights the major therapeutic effects of MSC administration as being paracrine-mediated. Along with expressing growth factors and cytokines, hWJ-MSCs secrete extracellular vesicles (exosomes) that have been shown to have immune-modulating, anti-inflammatory, antifibrotic, pro-angiogenic, and endogenous progenitor-cell activating effects.

In preclinical and clinical studies, hWJ-MSCs have shown promise in treating diseases affecting many tissues and organs. Major fields of study include osteoarthritis and other degenerative joint diseases, Graft-versus-Host Disease, wound healing, and neurologic disorders. Human WJ-MSCs possess a major advantage over other stem cells in safety due to their relative "immune-privileged" status. This allows for hWJ-MSCs to serve as an accessible, powerful tool in regenerative medicine.

Chondrogenic Differentiation of Human Wharton's Jelly of Umbilical Cord Derived Mesenchymal Stem Cells for Osteoarthritis Therapy

Osteoarthritis (OA) is a degenerative joint disease that commonly affects elderly or obese individuals. Treatment varies depending on severity and physician recommendation. Nadeem et al. aims to differentiate human Wharton's jelly-derived mesenchymal stem cells (hWJ-MSCs) into chondrocytes that could potentially be used for transplantation to treat OA.

hWJ-MSCs were isolated by explant culture. Proliferation rate, phenotype, and differentiation potential of hWJ-MSCs were determined. Expression of Sox9 (early-stage chondrocyte marker) and Col2a1 (mature stage chondrocyte marker) were high while expression of ACAN (mature stage chondrocyte marker) and Col10a1 (hypertrophic stage chondrocyte marker) were low in hWJ-MSCs following 28 days of chondrogenic induction media (Fig. 1A-D).

Gene expression over the course of differentiation (days 0, 3, 7, 14, 28) was compared to primary human knee chondrocytes serving as a positive control. Beta-catenin was significantly increased in day 28 samples compared to days 0-14 and positive control (Fig. 2). Sox9 expression was significantly higher at day 28 compared to days 0-14. Runx2 expression did not change significantly between days 3-14 however there was a significant increase in expression at day 28 compared to undifferentiated MSCs. This trend was similar for Col2a1, Col10a1, and ACAN however all remained significantly lower than the positive control. Immunoblot analysis showed that type II collagen protein was significantly increased in day-28 samples compared to undifferentiated MSCs while type X collagen protein remained low (Fig. 3).

Chondrocyte characterization by ICC, (A) Sox9 (green; nuclear marker), (B) Aggrecan (red), (C) type II collagen (green), (D) type X collagen (green).

Fig. 1. Chondrocyte characterization by ICC, (A) Sox9 (green; nuclear marker), (B) Aggrecan (red), (C) type II collagen (green), (D) type X collagen (green) (Nadeem G, Theerakittayakron K, et al., 2024).

Gene expression analysis of chondrocyte by qPCR: (A) Sox9, (B) Runx2, (C) Col2a1, (D) Col10a1, (E) ACAN, and (F) β-Catenin genes. The targeted gene was normalized to GAPDH as a reference gene, and the relative expression was calculated and compared to each group.

Fig. 2. Gene expression analysis of chondrocyte by qPCR: (A) Sox9, (B) Runx2, (C) Col2a1, (D) Col10a1, (E) ACAN, and (F) β-Catenin genes. The targeted gene was normalized to GAPDH as a reference gene, and the relative expression was calculated and compared to each group (Nadeem G, Theerakittayakron K, et al., 2024).

Type X collagen protein expression analysis of chondrocyte differentiated cells at day 28 by immunoblot, and β-actin protein was used as an internal control. Western blotting was carried out in duplicate.

Fig. 3. Type X collagen protein expression analysis of chondrocyte differentiated cells at day 28 by immunoblot, and β-actin protein was used as an internal control. Western blotting was carried out in duplicate (Nadeem G, Theerakittayakron K, et al., 2024).

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