4.5 Article

Bone Marrow Mesenchymal Stem Cells in Patients with Beta Thalassemia Major: Molecular Analysis with Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy Study as a Novel Method

期刊

STEM CELLS AND DEVELOPMENT
卷 21, 期 11, 页码 2000-2011

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/scd.2011.0444

关键词

-

资金

  1. METU internal funds
  2. Hacettepe University PEDI-STEM Project [2006 K 120 640]

向作者/读者索取更多资源

Bone marrow mesenchymal stem cells (BM-MSCs) are the main cellular components of the bone marrow, providing a supportive cellular microenvironment to maintain healthy hematopoiesis. beta-thalassemia major (beta-TM) is characterized by anemia that is caused by a genetic defect in hemoglobin synthesis and results in ineffective erythropoiesis (IE). The alterations in the microenvironment in thalassemic bone marrow during IE can cause changes in BM-MSCs. This study aimed to investigate global structural and compositional changes in BM-MSCs in beta-TM that may provide a basis in understanding interactions of hematopoietic stem cells (HSCs)-MSCs in such a pathological bone marrow microenvironment. Following characterization of morphological, immunophenotypical, and differentiation properties, the changes in healthy and thalassemic BM-MSCs before and after bone marrow transplantation (BMT) were examined by attenuated total reflection-Fourier transform infrared (ATR-FTIR). The significant increase in lipid, protein, glycogen, and nucleic acid contents in thalassemic BM-MSCs with respect to healthy BM-MSCs was attributed to enhanced cell proliferation and BM activity during IE. The significant decreases in the content of mentioned macromolecules in post-transplant group BM-MSCs versus pre-transplant BM-MSCs was interpreted as restoring effect of BMT therapy on IE and defective BM microenvironment. These alterations were also supported by ELISA results of erythropoietin (EPO) and growth differentiation factor (GDF15) in bone marrow plasma samples as a reflection of IE and by MTT proliferation assay on BM-MSCs. Based on these changes, sampling groups were discriminated by cluster analysis. These results provide information for the studies that concentrate on interactions between HSCs-MSCs in bone marrow.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Immunology

Long Term Follow-Up of the Patients with Severe Combined Immunodeficiency After Hematopoietic Stem Cell Transplantation: A Single-Center Study

Duygu Demirtas, Deniz Cagdas, Tuba Turul Ozgur, Baris Kuskonmaz, Duygu Uckan Cetinkaya, Ozden Sanal, Ilhan Tezcan

Summary: This study evaluated the outcomes of hematopoietic stem cell transplantation in 44 patients with severe combined immunodeficiency. The majority of patients showed normal immune reconstitution and growth after HSCT. It may be beneficial to use bone marrow instead of peripheral stem cells due to lower incidence of acute GVHD in bone marrow transplanted patients.

IMMUNOLOGICAL INVESTIGATIONS (2022)

Article Biotechnology & Applied Microbiology

Comparison of immune modulatory properties of human multipotent mesenchymal stromal cells derived from bone marrow and placenta

A. Sarikaya, G. Aydin, O. Ozyuncu, E. Sahin, D. Uckan-Cetinkaya, F. Aerts-Kaya

Summary: MSC can be isolated from tissues like bone marrow and placenta. There may be differences in differentiation and immunomodulation by MSC from different sources. Placenta-derived MSC showed higher proliferation rate compared to bone marrow MSC.

BIOTECHNIC & HISTOCHEMISTRY (2022)

Article Hematology

Pre-Conditioning Serum Uric Acid as a Risk Factor for Sinusoidal Obstruction Syndrome of the Liver in Children Undergoing Hematopoietic Stem Cell Transplantation

Fatma Visal Okur, Murat Karapapak, Khaled Warasnhe, Umut Ece Arslan, Baris Kuskonmaz, Duygu Cetinkaya

Summary: This study suggests that pre-conditioning serum UA is an independent risk factor for hepatic SOS after HSCT in children, and it may be used as an early predictor of SOS along with previously described clinical and laboratory parameters.

TURKISH JOURNAL OF HEMATOLOGY (2021)

Article Clinical Neurology

Effect of mesenchymal stem cells therapy in experimental kaolin induced syringomyelia model

Ercan Bal, Sahin Hanalioglu, Cagla Z. Kopru, Sevil Kose, Ahmet T. Basak, Sibel B. Pehlivan, Duygu U. Cetinkaya, Nuhan Purali, Petek Korkusuz, Gokhan Bozkurt

Summary: This study found that axonal repair in syringomyelia can be significantly improved through stem cell therapy. Stem cell treatment also promotes the organized reconstruction of tissue surrounding the syrinx cavity, accelerating the repair and regeneration of damaged axons. Therefore, stem cells may have potential therapeutic effects in the recovery of neural tissue and myelin damage in syringomyelia.

JOURNAL OF NEUROSURGICAL SCIENCES (2022)

Article Oncology

Intestinal mycobiota composition and changes in children with thalassemia who underwent allogeneic hematopoietic stem cell transplantation

Siddika Songul Yalcin, Tekin Aksu, Baris Kuskonmaz, Namik Yasar Ozbek, Vicente Perez-Brocal, Melda Celik, Duygu Uckan Cetinkaya, Andres Moya, Ener Cagri Dinleyici

Summary: This study evaluated the mycobiota composition pre- and post-HSCT in children with thalassemia, revealing a decrease in diversity following transplantation. Particularly, there was a predominance of Malassezia in children with GVHD. Further research is needed to understand this phenomenon in children with GVHD.

PEDIATRIC BLOOD & CANCER (2022)

Article Hematology

Association of Pre-Transplant Angiopoietin-2 Index with the Risk of Acute Graft-Versus-Host Disease after Hematopoietic Stem Cell Transplantation

Ozlem Satirer, Inci Cevher Zeytin, Berna Alkan, Jale Karakaya, Duygu Cetinkaya, Fatma Visal Okur

Summary: This study investigated the association between pre-transplant levels of angiogenic factors and the risk of acute graft-versus-host disease (aGvHD). The findings suggest that alterations in pre-transplant Ang2 levels may serve as an independent risk factor for aGvHD development.

TURKISH JOURNAL OF HEMATOLOGY (2022)

Article Cell Biology

Global miRNA expression of bone marrow mesenchymal stem/stromal cells derived from Fanconi anemia patients

Ilgin Cagnan, Mustafa Keles, Ayse Gokce Keskus, Melike Tombaz, Ozge Burcu Sahan, Fatima Aerts-Kaya, Duygu Uckan-Cetinkaya, Ozlen Konu, Aysen Gunel-Ozcan

Summary: Fanconi anemia (FA) is a rare genetic disorder characterized by genomic instability and bone marrow failure. This study investigated the miRNA profile of FA BM-MSCs before and after BM transplantation, with specific focus on miRNAs that may modulate BM mRNA networks in FA patients, revealing potential candidates for further research.

HUMAN CELL (2022)

Article Hematology

Hematopoietic stem cell transplantation for adolescents and adults with inborn errors of immunity: an EBMT IEWP study

Michael H. Albert, Tiarlan Sirait, Dirk-Jan Eikema, Katerina Bakunina, Claudia Wehr, Felipe Suarez, Maria Laura Fox, Nizar Mahlaoui, Andrew R. Gennery, Arjan C. Lankester, Rita Beier, Maria Ester Bernardo, Venetia Bigley, Caroline A. Lindemans, Siobhan O. Burns, Ben Carpenter, Jaroslaw Dybko, Tayfun Gungor, Fabian Hauck, Su Han Lum, Dmitry Balashov, Roland Meisel, Despina Moshous, Ansgar Schulz, Carsten Speckmann, Mary A. Slatter, Brigitte Strahm, Duygu Uckan-Cetinkaya, Isabelle Meyts, Tanja C. Vallee, Robert Wynn, Benedicte Neven, Emma C. Morris

Summary: Allogeneic hematopoietic stem cell transplantation (HSCT) is the gold standard curative therapy for infants and children with inborn errors of immunity (IEI), but its adoption for adolescents and adults with IEI has been delayed due to lack of outcome data and perceived high risk of transplant-related mortality. This large retrospective, multicenter study reports on 329 IEI patients who underwent HSCT between 2000 and 2019. The study found that the overall survival (OS) and event-free survival (EFS) rates were 78% and 65% at 1 year post-HSCT, and 71% and 62% at 5 years post-HSCT, respectively. The study also identified risk factors for adverse outcomes, providing important evidence for patient selection.
Letter Biophysics

First allogeneic hematopoietic stem cell transplantation in RASGRP1 deficiency: long-term follow-up

Baris Kuskonmaz, Deniz Ayvaz, Fatma Visal Okur, Burca Aydin, Ilhan Tezcan, Duygu Uckan Cetinkaya

BONE MARROW TRANSPLANTATION (2022)

Article Biophysics

Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience

M. Akif Yesilipek, Vedat Uygun, Alphan Kupesiz, Gulsun Karasu, Gulyuz Ozturk, Mehmet Ertem, Ilgen Sasmaz, Hayriye Daloglu, Elif Guler, Volkan Hazar, Tunc Fisgin, Gulay Sezgin, Savas Kansoy, Baris Kuskonmaz, Burcu Akinci, Namik Ozbek, Elif Unal Ince, Seda Ozturkmen, Funda Tayfun Kupesiz, Koray Yalcin, Sema Anak, Ceyhun Bozkurt, Musa Karakukcu, Serhan Kupeli, Davut Albayrak, Haldun Oniz, Serap Aksoylar, Fatma Visal Okur, Canan Albayrak, Fatma Demir Yenigurbuz, Ikbal Ok Bozkaya, Talia Ileri, Orhan Gursel, Barbaros Sahin Karagun, Gulen Tuysuz Kintrup, Suna Celen, Murat Elli, Basak Adakli Aksoy, Ebru Yilmaz, Atila Tanyeli, Sule Turan Akyol, Zuhal Onder Sivi, Gulcihan Ozek, Duygu Uckan, Ibrahim Kartal, Didem Atay, Arzu Akyay, Ozlem Arman Bilir, Hasan Fatih Cakmakl, Emin Kurekci, Baris Malbora, Sinan Akbayram, Haci Ahmet Demir, Suar Caki Kilic, Adalet Meral Gunes, Emine Zengin, Salih Ozmen, Ali Bulent Antmen

Summary: The study analyzed national data on hematopoietic stem cell transplantation for thalassemia major patients in Turkey, finding that transplanting before the age of 7 with a matched donor can improve outcomes, and that different time points and donor types have varying impacts on transplant results.

BONE MARROW TRANSPLANTATION (2022)

Article Genetics & Heredity

Combined immunodeficiency due to purine nucleoside phosphorylase deficiency: Outcome of three patients

Basak Torun, Ahmet Bilgin, Diclehan Orhan, Rahsan Gocmen, Sebnem Sara Kilic, Baris Kuskonmaz, Duygu Cetinkaya, Ilhan Tezcan, Deniz Cagdas

Summary: PNP deficiency caused by mutations in the PNP gene can result in immunodeficiency and various clinical symptoms. Hematopoietic stem cell transplantation is the only available treatment and can improve neurological symptoms and developmental delay.

EUROPEAN JOURNAL OF MEDICAL GENETICS (2022)

Article Biochemical Research Methods

The structural effects of Vitamin A deficiency on biological macromolecules due to ethanol consumption and withdrawal: An FTIR study with chemometrics

Birsen Elibol, Mete Severcan, Ewa Jakubowska-Dogru, Ilknur Dursun, Feride Severcan

Summary: The structural effects of vitamin A deficiency on the molecular profiles of biomolecules in the male rat hippocampus during prolonged ethanol intake/withdrawal were investigated using FT-IR spectroscopy and chemometrics. The study found that ethanol consumption/withdrawal caused significant changes in the conformation of proteins, while having minimal structural effects on lipids. In the presence of vitamin A deficiency, ethanol induced structural changes in lipids, particularly in the early ethanol withdrawal stage. Moreover, an increase in lipid and protein content, an increase in the saturated/unsaturated lipid ratio, a decrease in nucleic acids content, and a decrease in membrane fluidity were observed. These changes were less severe in the presence of vitamin A.

JOURNAL OF BIOPHOTONICS (2022)

Article Pediatrics

Predictors of kidney complications and analysis of hypertension in children with allogeneic hematopoietic stem cell transplantation

Anar Gurbanov, Bora Gulhan, Baris Kuskonmaz, Fatma Visal Okur, Fatih Ozaltin, Ali Duzova, Duygu Uckan Cetinkaya, Rezan Topaloglu

Summary: This study aimed to determine the incidence of kidney complications in pediatric allogeneic hematopoietic stem cell transplantation patients. The results showed a higher incidence of acute kidney injury, with primary malignant disease and viral infection being associated with an increased risk. Additionally, 24-hour ambulatory blood pressure monitoring played an important role in monitoring hypertension in these patients.

PEDIATRIC NEPHROLOGY (2023)

Article Cell & Tissue Engineering

Alterations in Hematopoietic and Mesenchymal Stromal Cell Components of the Osteopetrotic Bone Marrow Niche

Inci Cevher Zeytin, Berna Alkan, Cansu Ozdemir, Duygu Uckan Cetinkaya, Fatma Visal Okur

Summary: This study investigates the alterations in the HSC and MSC components of the osteopetrotic niche, as well as their interactions, to mimic stem cell dynamics/trafficking in the bone marrow niche after HSC transplantation. The findings suggest significant changes in both the MSC and HPC compartments of the osteopetrotic niche and highlight the impact of functionally impaired osteoclasts on defective niche formation.

STEM CELLS TRANSLATIONAL MEDICINE (2022)

Article Immunology

A single-center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class- Switch Recombination defects

Aysegul Akarsu, Sevil Halacli, Cagman Tan, Baris Kuskonmaz, Alphan Kupesiz, Duygu Cetinkaya, Ozden Sanal, Ilhan Tezcan, Deniz Cagdas

Summary: Patients with CSR defects and HIGM phenotype exhibit diverse clinical manifestations and laboratory features. CD40L deficiency patients show low IgM levels, neutropenia, and eosinophilia prominently.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY (2022)

暂无数据