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All Journal Medical Journal of Indonesia Indonesian Journal of Cancer Ibnu Sina: Jurnal Kedokteran dan Kesehatan - Fakultas Kedokteran Universitas Islam Sumatera Utara

Lia Damayanti

Departement of Histology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia

Author-ID : 249135

Humanities Biochemistry, Genetics & Molecular Biology Health Professions Immunology & microbiology Medicine & Pharmacology Public Health

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Articles

Comparison of various procedures in the processing of binucleated-lymphocytes on to glass slide to detect chromosomal breakage Pawitan, Jeanne A.; Suryono, Isnani A.; Damayanti, Lia; Purbadi, Sigit
Medical Journal of Indonesia Vol 12, No 1 (2003): January-March
Publisher : Faculty of Medicine Universitas Indonesia

Binucleated lymphocytes can be screened for micronuclei to assess chromosomal damage. There are various procedures to get slides containing binucleated lymphocytes, that are different in harvesting, fixation, and slide preparation methods. Screening binucleated lymphocytes to find a micronucleus needs at least 800 cells with intact cytoplasm. This study aimed to analyze the various procedures and simplified procedures to know which procedure gave the most abundant binucleated lymphocytes with intact cytoplasm and best staining properties for the purpose of micronucleus scoring. Seven heparinized blood samples were obtained from the Dept. of Obstetrics and gynecology, Faculty of medicine, University of Indonesia, Jakarta. The 7 blood samples were subjected to 17 procedures different in harvesting (with or without washing), slide preparation (smear and spot method, and using a cytocentrifuge), and fixation methods (methanol for 1 minute, methanol brief, methanol/glacial acetic acid 3:1 or 9:1). Our results showed that fixatives containing glacial acetic acid are not suitable for micronucleus test. To generate binucleated lymphocytes with intact cytoplasm as much as possible, the procedure should be conducted without washing steps. Methanol fixation either briefly or 1 minute is preferable, and for the ease of screening cytocentrifuge preparation, followed by spot method is preferable. (Med J Indones 2003; 12: 3-7)Â Keywords: cytokinesis blocked, spot, smear, cytocentrifuge, fixatives

Effect of adipose tissue processing procedures in culture result: a study preliminary Pawitan, Jeanne A.; Bustami, Arleni; Damayanti, Lia; Antarianto, Radiana D.; Swantari, Ni M.
Medical Journal of Indonesia Vol 20, No 1 (2011): February
Publisher : Faculty of Medicine Universitas Indonesia

Background: There are various methods of processing adipose tissue before culture, depending on the adipose tissue samples. The aim of this study is to compare several modifications of culturing and sub-culturing procedures of adipose tissue to fit the condition in our laboratory.Method: This is a descriptive study that was done in the Immunology and Endocrinology Integrated Laboratory, University of Indonesia, fromÂ October 2009 to April 2010. Three adipose tissue processing procedures, various amount of seeding and two subculture methods were compared in term of cell yield and time needed. In the first procedure, collagenase-1 digestion was done in 30minutes, cell seeding were 24,000 and 36,000 per flask; in the second procedure, collagenase-1 digestion was done in 60minutes, cell seeding were 24,000, 48,000, and 72,000 per flask; and in the third procedure, the adipose tissue remnants from the firstÂ procedure were again digested for another 45 minutes, cell seeding were 74,000, and 148,000 per flask. Difference in subculture methods were the presence or absence of washing step.Result: Procedure 1 yielded the lowest amount of cell, and after culture, the cells grew very slow, and was contaminated before harvest of primary culture. Procedure-2 and -3 succeeded to yield primary cultures. Some of the cultures were contaminated, so that further subculture was notÂ applicable, and only one tissue processing procedure (procedure 2: 60 minute collagenase-1 digestion, without lysis buffer, cell seeding 48,000 and 72,000) could complete the three subcultures. Though some of the procedures could not be completed, final result could be concluded.Conclusion: In this preliminary study, 60 minute colagenase-1 digestion with intermittent shaking every 5 minutes and cell seeding around 50,000 or more, followed by subculture method without washing step gave the best result. (Med J Indones 2011; 20:15-9)Keywords: collagenase-1, primary culture, subculture, stromal-vascular fraction

Cytology technique: development of a simple spot method for cultured cell suspension Pawitan, Jeanne A.; Damayanti, Lia; Arleni, Arleni; Swantari, Ni M.
Medical Journal of Indonesia Vol 19, No 1 (2010): February
Publisher : Faculty of Medicine Universitas Indonesia

Aim To develop a simple spot method to attach cultured cells in suspension on to a glass slide.Methods We compared three approaches using both conventional and special glass slide (Shandon-Polysin), either without additional fetal bovine serum (FBS), or with addition of 3 or 10 Î¼l of FBS to a 20 Î¼l sample (altogether there were six approaches). The slides were examined qualitatively for the background color, boundary color and intactness, and whether there were folded and detached parts. Further, for each slide, the attached intact cells were counted, and the percentage of attached intact cells per number of spotted cells was calculated. The difference in attach intact cells between different approaches was analyzed by ANOVA using SPSS 13.0 for windows.Results There were no significant difference in the percentage of attached intact cells between the six approaches (P= 0.804), though the approach using special glass slide without additional FBS (FBS final concentration 5%) yield the highest percentage of attached intact cells, showed clean background without folded parts.Conclusions We have developed a simple spot method for cultured cell suspension, and the best approach to make spot specimen is using special glass slide with 5% FBS in the cell suspension. (Med J Indones 2010; 19:26-31)Keywords: spot specimen, special glass slide, fetal bovine serum

Adipose derived stem cell conditioned medium effect on proliferation phase of wound healing in Sprague Dawley rat Tarcisia, Twidy; Damayanti, Lia; Antarianto, Radiana D.; Moenadjat, Yefta; Pawitan, Jeanne A.
Medical Journal of Indonesia Vol 26, No 4 (2017): December
Publisher : Faculty of Medicine Universitas Indonesia

Background: Disintegration of skin tissue can lead to disability and death. Recent studies on wound therapy applied stem cells and adipose derived stem cell conditioned medium (ADSC-CM) to improve wound healing. However, the role of ADSC-CM in wound healing mechanism in terms of angiogenesis, quantity of collagen, and epithelialization is not fully understood. Therefore, this study aimed to analyze the levels of growth factors (VEGF and EGF) in ADSC-CM and histological features of angiogenesis, epithelialization, and collagen density after skin incision in Sprague Dawley rats.Methods: Thirty rats were injured at the back (full thickness wound) and treated topically with ADSC-CM, culture medium, basal medium, and without treatment. Mice were sacrificed on days 3, 7, 14, 21 and 28. After sacrificed, tissue samples were examined microscopically to assess angiogenesis, epithelialization, and collagen density. Concentrations of VEGF and EGF in ADSC-CM were measured by ELISA.Results: Clinically, wound that was treated with ADSC-CM showed improvement in wound healing process. ADSC-CM treated wound showed the highest epithelialization ratio and the fastest wound closure.Conclusion: There were no statistical significant differences between groups that were treated with ADSC-CM and not. However, topical ADSC-CM treated wound revealed a better clinical improvement in epithelialization.

Comparison of fetal bovine serum and platelet-rich plasma on human lipoaspirate-derived mesenchymal stem cell proliferation Suryani, Des; Pawitan, Jeanne A.; Lilianty, Jinia; Purwoko, Reza Y.; Liem, Isabella K.; Damayanti, Lia
Medical Journal of Indonesia Vol 22, No 3 (2013): August
Publisher : Faculty of Medicine Universitas Indonesia

Background: Lipoaspirate-derived stem cells (LSCs) are very promising for regenerative medicine, e.g. to treat acute myocard infarction. Fetal bovine serum (FBS) is commonly used to propagate the LSCs. However, for its clinical application, FBS contains xeno-proteins that are potential to elicit immune rejection in patients. Platelet rich plasma (PRP) is one of the candidates to replace FBS. This study was aimed to compare the proliferation of LSCs cultured in 5% PRP, 10% PRP, and FBS containing medium (MesenCult®).Methods: LSCs were cultured in 5% PRP/DMEM, 10% PRP/DMEM, and MesenCult®. After the primary culture reached its confluency, cells were harvested using TrypLE Select and seeded (around 20,000 viable cells) in new vessels in the same media. Passages were done until passage-5, with six replications. Population doubling time (PDT) of the three groups were analyzed using Kruskal Wallis test.Results: LSCs showed different proliferation rates when cultured in 5% PRP/DMEM, 10% PRP/DMEM, and MesenCult®. PDT of the three experimental groups in passage 1-5 were significanly different (p < 0.05), with the lowest rank was cultured in medium of 10% PRP/DMEM.Conclusion: The results suggest that 10% PRP/DMEM can be used as an alternative to replace FBS in LSC culture. (Med J Indones. 2013;22:146-51. doi: 10.13181/mji.v22i3.583)Keywords: Fetal bovine serum, lipoaspirate, platelet rich plasma, stem cell

Stimulation Effect of Exosome From Healthy Sera to Natural Killer (NK) Cells of Hepatocellular Carcinoma Subject In Vitro Deby, Deby; Antarianto, Radiana Dhewayani; Barasila, Atikah Chalida; Irawan, Cosphiadi; Ahani, Ardhi Rahman; Jasirwan, Chyntia Olivia Maurine; Damayanti, Lia; Ritchie, Ni Ken; Aditya, Robby Nur
Indonesian Journal of Cancer Vol 18, No 4 (2024): December
Publisher : http://dharmais.co.id/

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33371/ijoc.v18i4.1122

Background: Hepatocellular carcinoma has a poor prognosis due to limitations of therapy such as late diagnosis, lack of specific biomarkers, and insensitivity to this tumor agent. This study aims to develop immunotherapy using autologous natural killer cells (NK cells) with exosome stimulation for hepatocellular carcinoma patients, addressing treatment limitations.Methods: Experimental research conducted from October 2022 to June 2023 at Universitas Indonesia’s Faculty of Medicine involved three hepatocellular carcinoma patients at Dr. Cipto Mangunkusumo General Hospital in Jakarta, Indonesia. NK cells from hepatocellular carcinoma patients were isolated from peripheral venous blood, and exosomes were isolated from the blood serum of healthy donors. Exosome characterization with a particle size analyzer and flow cytometry. Stimulation of exosomes on NK cells for 24 hours, then evaluation of expression of NKp44, NKp46, NKp30, NKG2D, KIR2D, and NKG2A receptors, as well as perforin and granzyme B expression. Visualization of interactions of NK cells with other mononuclear cell fractions (CD4, CD8, CD11c, and CD19) by immunofluorescence. The study compares stimulated and unstimulated NK cells, analyzing their expression of activated and inhibitory receptors, using either the One-Way Anova parametric test or the Kruskal-Wallis non-parametric test for non-normally distributed data.Results: Particle size 100 nm, negative electric charge, and CD63+CD81+ (double positive) exosome isolated results. There was increased expression of receptors NKp44, NKp46, NKp30, NKG2D, decreased expression of NKG2A, and increased expression of perforin and granzyme B in exosome-induced NK cells. There was no cell interaction in the form of immune synapses between exosome-induced NK cells and other mononuclear cell fractions in hepatocellular carcinoma patients. Conclusions: Induction of exosomes into NK cells of hepatocellular carcinoma patients restores the cytotoxic ability of NK cells

PERAN RASIO LACTATE DEHIDROGINASE DAN LIMFOSIT SEBAGAI PENANDA EFUSI PLEURA MALIGNANSI: THE ROLE OF LACTATE DEHYDROGENASE AND LYMPHOCYTE RATIO AS MARKERS OF MALIGNANT PLEURAL EFFUSION Pasaribu, Rouly Pola; Damayanti, Lia
Ibnu Sina: Jurnal Kedokteran dan Kesehatan - Fakultas Kedokteran Universitas Islam Sumatera Utara Vol. 24 No. 2 (2025): Juli 2025
Publisher : Faculty of Medicine Universitas Islam Sumatera Utara

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30743/ibnusina.v24i2.913

Pendahuluan: Efusi pleura merupakan salah satugejala dari patologi yang mendasarinya. Pemeriksaan biokimia yang umumnya dilakukan untuk membedakan patologi tersebut adalah kadar laktat dehydrogenase, adenosine deaminase, dan limfosit. Tujuan: mengevaluasi penggunaan rasio LDH cairan pleura/limfosit dalam cairan pleura sebagai parameter baru untuk membedakan antara efusi pleura maligna dan bukan. Metode: Penelitian cross sectional di RSUP Dr. Mohammad Hoesin (RSMH) Palembang menggunakan rekam medis. Pasien dewasa dengan diagnosa efusi pleura eksudatif yang dilakukan pemeriksaan analisa cairan pleura libatkan dalam penelitian ini. Uji hipotesis dilakukan dengan menggunakan uji T tidak berpasangan atau uji Mann Whitney U. Hasil: Penelitian ini melibatkan 206 pasien, dimana 43,21% didiagnosis dengan efusi pleura non-malignansi, sedangkan 56,79% dengan efusi pleura malignansi. Pemeriksaan LDH cairan pleuradan limfosit cairan pleura menunjukkan perbedaan yang signifikan antara kelompok pasien dengan dan tanpa malignansi (LDH cairan pleurakelompok malignansi: 593,5 U/L [32 – 1.940] vs kelompok non-malignansi: 198 U/L [104 – 811], p < 0,001; limfosit kelompok non-malignansi: 87% [21-95] vs kelompok malignansi: 38% [30-93], p < 0,001). Rasio LDH cairan pleura terhadap limfosit juga menunjukkan perbedaan yang signifikan (kelompok malignansi: 15,18 [0,81-60,03] vs non-malignansi: 2,84 [1,15-22,87], p < 0,001). Kesimpulan: Terdapat perbedaan yang signifikan antara LDH cairan pleura, limfosit cairan pleura, dan rasio antara kedua antara pasien dengan efusi pleura maligna dan non-maligna.

Co-Authors Aditya, Robby Nur Ahani, Ardhi Rahman Antarianto, Radiana Dhewayani Arleni Arleni Arleni Bustami Barasila, Atikah Chalida Chyntia Olivia Maurine Jasirwan, Chyntia Olivia Maurine Cosphiadi Irawan Deby Deby Des Suryani Isabella K. Liem Isnani A. Suryono Jeanne A. Pawitan Jinia Lilianty Ni Ken Ritchie, Ni Ken Ni M. Swantari Pasaribu, Rouly Pola Radiana D. Antarianto Reza Y. Purwoko Sigit Purbadi Twidy Tarcisia, Twidy Yefta Moenadjat

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