Sains Malaysiana 52(11)(2023): 3103-3119

http://doi.org/10.17576/jsm-2023-5211-07

 

The Optimal Cryo Revival Period of Cryopreserved Wharton's Jelly Derived-Mesenchymal Stem Cells

(Tempoh Pemulihan Krio Optimum bagi Sel Stem Mesenkima Wharton Jeli yang Diawet Krio)

 

VIKNESWARY RAVI KUMAR1,2, MOHAMAD FIKERI ISHAK2, SHARIFAH IZWAN TUAN OTHMAN1, TRISTAN TAN3 & YOGESWARAN LOKANATHAN2,*

 

1University Selangor (UNISEL, Shah Alam City Campus, Selangor), Jalan Zirkon A7/A, Seksyen 7, 40000 Shah Alam, Selangor, Malaysia

2Centre for Tissue Engineering and Regenerative Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaacob Latiff, Bandar Tun Razak, 56000 Cheras, Kuala Lumpur, Malaysia

 3Da Vinci Healife Sdn. Bhd. 13-2, The Boulevard Offices, Mid Valley City, 59200 Kuala Lumpur, Malaysia

 

Received: 12 May 2023/Accepted: 20 October 2023

 

Abstract

The workflow of cryopreservation is a challenging step in the standardised preparation of cell therapy products in terms of methods used (i.e., adapted controls of the work environment, quality control, reagents, and equipment). This study aimed to determine the effect of cryopreservation on the stability of mesenchymal stem cell (MSC) characteristics by comparing fresh cells with those that underwent different post-thaw cell recovery periods. The MSCs were derived from human Wharton’s jelly umbilical cord (n = 4). The cells that were cryopreserved for 7 days were revived at 0 h (CRC-0h), 24 h (CRC-24h) and 7 days (CRC-7d) and then evaluated on the basis of cell viability, doubling time, morphology, trilineage differentiation potential, growth kinetics, and MSC surface marker expression. The cell viability of the CRC-0h group was 90%, whereas that of the CRC-24h group was 80%-85%. Cell attachment results showed that CRC-24h had a notably higher attachment rate than the other two groups. The CRC groups showed CD90, CD73 or CD44 expression, which meets the minimum criteria for defining multipotent MSCs. By contrast, CD105 expression was significantly reduced in the CRC groups and was lower than the minimum requirement based on the standards of the International Society for Cellular Therapy. Results suggest that at least 24 h is necessary to improve the quality of MSCs for it to be adequate for cell therapy use.

 

Keywords: Cell therapy; cryopreservation; cryorevival; mesenchymal stromal cell; recovery period

 

Abstract

Aliran kerja pengawetan krio ialah satu langkah yang mencabar dalam penyediaan piawai produk terapi sel daripada segi kaedah yang digunakan (seperti kawalan disesuaikan persekitaran kerja, kawalan kualiti, reagen dan peralatan). Kajian ini bertujuan untuk menentukan kesan pengawetan krio ke atas kestabilan ciri sel stem mesenkima (MSC) dengan membandingkan sel segar dengan sel yang menjalani tempoh pemulihan sel pasca nyahbeku yang berbeza. MSC diperoleh daripada tali pusat jeli Wharton manusia (n = 4). Sel yang diawet krio selama 7 hari telah dihidupkan semula pada 0 jam (CRC-0j), 24 jam (CRC-24j) dan 7 hari (CRC-7h) dan kemudian dinilai berdasarkan daya maju sel, masa gandaan, morfologi, potensi pembezaan trilineage, kinetik pertumbuhan dan ekspresi penanda permukaan MSC. Daya maju sel kumpulan CRC-0j ialah 90%, manakala kumpulan CRC-24j ialah 80%–85%. Keputusan pelekatan sel menunjukkan bahawa CRC-24j mempunyai kadar pelekatan yang lebih tinggi daripada dua kumpulan lain. Kumpulan CRC menunjukkan ekspresi CD90, CD73 atau CD44 yang memenuhi kriteria minimum untuk menentukan MSC multipoten. Sebaliknya, ekspresi CD105 berkurang dengan ketara dalam kumpulan CRC dan lebih rendah daripada keperluan minimum berdasarkan piawaian International Society for Cellular Therapy. Keputusan menunjukkan bahawa sekurang-kurangnya 24 jam diperlukan untuk meningkatkan kualiti MSC supaya ia mencukupi untuk kegunaan terapi sel.

 

Kata kunci: Pemulihan krio; pengawetan krio; sel stromal mesenkima; tempoh pemulihan; terapi sel

 

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*Corresponding author; email: lyoges@ppukm.ukm.edu.my

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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