A Tribute to Professor Alexander Friedenstein and His Outstanding Achievements in the Area of Stromal Stem Cells

A special issue of Bioengineering (ISSN 2306-5354). This special issue belongs to the section "Regenerative Engineering".

Deadline for manuscript submissions: closed (31 May 2024) | Viewed by 10569

Special Issue Editors


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Guest Editor
Leeds Institute of Molecular Medicine, School of Medicine, University of Leeds, Leeds LS2 9JT, UK
Interests: mesenchymal stem cells/multipotential stromal cells (MSCs); bone regeneration; cartilage regeneration; osteoarthritis; regenerative medicine; regenerative orthopedics; MSC senescence
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Guest Editor
Department of Orthopaedics, Division of Sports Medicine, Diabetes Research Institute, Cell Transplant Center, University of Miami, Miller School of Medicine, 1450NW 10th Ave, Room 3012, Miami, FL 33136, USA
Interests: mesenchymal stem cells/multipotential stromal cells (MSCs); MSC trophic and immunomodulatory actions; MSC functionalization ex vivo; inflammation and fibrosis reversal; synovitis; osteoarthritis; regenerative sports medicine; regenerative orthopaedics
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Guest Editor
Department of Biology, Case Western Reserve University, Cleveland, OH, USA
Interests: mesenchymal stem cells/multipotential stromal cells (MSCs); cartilage repair and regeneration; mechanisms of bone invasion during metastasis

Special Issue Information

Dear Colleagues,

Professor Alexander Friedenstein is credited as the discoverer of stromal progenitor cells, later called mesenchymal stem cells (MSCs). He defined them as stroma-resident cells that are (1) highly proliferative and clonogenic in vitro and (2) capable of extensive self-renewal and multi-lineage differentiation in vivo, thus fulfilling the main criteria attributed to stem cells. Using several in vivo transplantation models, he and his colleagues were able to demonstrate that single-cell-derived clones of stromal progenitors had an intrinsic ability to form bone, cartilage and connective tissues in vivo. This achievement is hard to underestimate, not only in terms of stem cells in general, but also in terms of cell therapies and tissue engineering developments that followed on from his discovery and continue to grow exponentially to the present day.

Alexander Friedenstein was born on the 24th of June 1924 in Kyiv. His family relocated to Moscow in 1928, where he graduated with a degree in Medicine in 1946. In 1950, he obtained a PhD in skeletal regeneration in high vertebrates, and in 1960, he was awarded a higher doctorate on the histological origins of extra-skeletal osteogenesis. In the late 1960s and early 1970s, he published a number of seminal articles on stromal precursor cells for osteogenic tissues that were later popularised and disseminated worldwide through his collaboration with Dr Maureen Owen in Oxford. In 1991, Dr Arnold Caplan coined the term MSCs to refer to these stromal progenitors; although this terminology remains a matter of active debate, it continues to provoke a tremendous amount of interest in the scientific community. Cell therapy applications with MSCs or their derivatives (secretomes, extracellular vesicles, etc) continue to expand into medical fields beyond skeletal regeneration. MSC-based bioinks are being used in tissue regeneration and disease modelling. For the bioengineering community, the works of Alexander Friedenstein remain highly influential and open up new avenues for further exploration, for example:

  1. How can we best isolate and culture MSCs in order to maximise their desired function(s)?
  2. The in vivo tissue identity of MSCs as perivascular cells and the therapeutic implications of this identity; MSC migration.
  3. How can we enhance the desired functions of endogenous MSCs?
  4. The heterogeneity of cultures of MSCs as they relate to their clinical effects.
  5. How can we control MSC differentiation or trophic activity through their microenvironment, including smart biomaterials?
  6. How can we effectively isolate MSCs-derived extracellular vesicles and what are the methods that can be used to reinforce their therapeutic signatures?
  7. What are the benefits and limitations of MSCs versus MSC-derived extracellular vesicles for therapeutics?

On the occasion of Professor Alexander Friedenstein’s centenary in June 2024, Drs Elena Jones, Dimitrios Kouroupis and Rodrigo Somoza are editing a Special Issue entitled "Tribute to Professor Alexander Friedenstein and His Outstanding Achievements in the Area of Stromal Stem Cells" to celebrate his memory. Contributions can take the form of original research articles or reviews that include, but not limited to, the above aspects of his legacy, as well as any new developments in the area of MSCs and their applications in regenerative medicine.

Dr. Elena A. Jones
Dr. Dimitrios Kouroupis
Dr. Rodrigo Somoza
Guest Editors

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Published Papers (6 papers)

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Editorial

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7 pages, 1556 KiB  
Editorial
The Collaborative Spark That Ignited the Field of Stromal Stem Cell Biology
by James T. Triffitt
Bioengineering 2024, 11(7), 652; https://doi.org/10.3390/bioengineering11070652 - 26 Jun 2024
Viewed by 1242
Abstract
Russia has produced many scientists of great renown in a multitude of fields from chemistry, physics, astronautics, and mathematics to biology, pathology, and medicine [...] Full article
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3 pages, 192 KiB  
Editorial
Mesenchymal Stem/Stromal Cell-Derived Small Extracellular Vesicles (MSC-sEVs): A Promising Treatment Modality for Diabetic Foot Ulcer
by Dimitrios Kouroupis, Lee D. Kaplan, Camillo Ricordi and Thomas M. Best
Bioengineering 2023, 10(10), 1140; https://doi.org/10.3390/bioengineering10101140 - 28 Sep 2023
Cited by 2 | Viewed by 1219
Abstract
Diabetic foot ulcer (DFU) is associated with neuropathy and/or peripheral artery disease of the lower limb in diabetic patients, affecting quality of life and leading to repeated hospitalizations and infections [...] Full article

Review

Jump to: Editorial

13 pages, 2959 KiB  
Review
Alexander Friedenstein, Mesenchymal Stem Cells, Shifting Paradigms and Euphemisms
by Donald G. Phinney
Bioengineering 2024, 11(6), 534; https://doi.org/10.3390/bioengineering11060534 - 23 May 2024
Viewed by 1303
Abstract
Six decades ago, Friedenstein and coworkers published a series of seminal papers identifying a cell population in bone marrow with osteogenic potential, now referred to as mesenchymal stem cells (MSCs). This work was also instrumental in establishing the identity of hematopoietic stem cell [...] Read more.
Six decades ago, Friedenstein and coworkers published a series of seminal papers identifying a cell population in bone marrow with osteogenic potential, now referred to as mesenchymal stem cells (MSCs). This work was also instrumental in establishing the identity of hematopoietic stem cell and the identification of skeletal stem/progenitor cell (SSPC) populations in various skeletal compartments. In recognition of the centenary year of Friedenstein’s birth, I review key aspects of his work and discuss the evolving concept of the MSC and its various euphemisms indorsed by changing paradigms in the field. I also discuss the recent emphasis on MSC stromal quality attributes and how emerging data demonstrating a mechanistic link between stromal and stem/progenitor functions bring renewed relevance to Friedenstein’s contributions and much needed unity to the field. Full article
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19 pages, 1316 KiB  
Review
Role of Mesenchymal Stem/Stromal Cells (MSCs) and MSC-Derived Extracellular Vesicles (EVs) in Prevention of Telomere Length Shortening, Cellular Senescence, and Accelerated Biological Aging
by Myrna Y. Gonzalez Arellano, Matthew VanHeest, Sravya Emmadi, Amal Abdul-Hafez, Sherif Abdelfattah Ibrahim, Ranga P. Thiruvenkataramani, Rasha S. Teleb, Hady Omar, Tulasi Kesaraju, Tarek Mohamed, Burra V. Madhukar and Said A. Omar
Bioengineering 2024, 11(6), 524; https://doi.org/10.3390/bioengineering11060524 - 21 May 2024
Cited by 1 | Viewed by 1857
Abstract
Biological aging is defined as a progressive decline in tissue function that eventually results in cell death. Accelerated biologic aging results when the telomere length is shortened prematurely secondary to damage from biological or environmental stressors, leading to a defective reparative mechanism. Stem [...] Read more.
Biological aging is defined as a progressive decline in tissue function that eventually results in cell death. Accelerated biologic aging results when the telomere length is shortened prematurely secondary to damage from biological or environmental stressors, leading to a defective reparative mechanism. Stem cells therapy may have a potential role in influencing (counteract/ameliorate) biological aging and maintaining the function of the organism. Mesenchymal stem cells, also called mesenchymal stromal cells (MSCs) are multipotent stem cells of mesodermal origin that can differentiate into other types of cells, such as adipocytes, chondrocytes, and osteocytes. MSCs influence resident cells through the secretion of paracrine bioactive components such as cytokines and extracellular vesicles (EVs). This review examines the changes in telomere length, cellular senescence, and normal biological age, as well as the factors contributing to telomere shortening and accelerated biological aging. The role of MSCs—especially those derived from gestational tissues—in prevention of telomere shortening (TS) and accelerated biological aging is explored. In addition, the strategies to prevent MSC senescence and improve the antiaging therapeutic application of MSCs and MSC-derived EVs in influencing telomere length and cellular senescence are reviewed. Full article
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12 pages, 1880 KiB  
Review
Recent Advances of MSCs in Renal IRI: From Injury to Renal Fibrosis
by Xinhao Niu, Xiaoqing Xu, Cuidi Xu, Yin Celeste Cheuk and Ruiming Rong
Bioengineering 2024, 11(5), 432; https://doi.org/10.3390/bioengineering11050432 - 27 Apr 2024
Viewed by 1381
Abstract
Renal fibrosis is a pathological endpoint of maladaptation after ischemia-reperfusion injury (IRI), and despite many attempts, no good treatment has been achieved so far. At the core of renal fibrosis is the differentiation of various types of cells into myofibroblasts. MSCs were once [...] Read more.
Renal fibrosis is a pathological endpoint of maladaptation after ischemia-reperfusion injury (IRI), and despite many attempts, no good treatment has been achieved so far. At the core of renal fibrosis is the differentiation of various types of cells into myofibroblasts. MSCs were once thought to play a protective role after renal IRI. However, growing evidence suggests that MSCs have a two-sided nature. In spite of their protective role, in maladaptive situations, MSCs start to differentiate towards myofibroblasts, increasing the myofibroblast pool and promoting renal fibrosis. Following renal IRI, it has been observed that Bone Marrow-Derived Mesenchymal Stem Cells (BM-MSCs) and Renal Resident Mesenchymal Stem Cells (RR-MSCs) play important roles. This review presents evidence supporting their involvement, discusses their potential mechanisms of action, and suggests several new targets for future research. Full article
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17 pages, 4764 KiB  
Review
Mesenchymal Stem/Stromal Cells: Immunomodulatory and Bone Regeneration Potential after Tumor Excision in Osteosarcoma Patients
by Max Baron, Philip Drohat, Brooke Crawford, Francis J. Hornicek, Thomas M. Best and Dimitrios Kouroupis
Bioengineering 2023, 10(10), 1187; https://doi.org/10.3390/bioengineering10101187 - 13 Oct 2023
Cited by 5 | Viewed by 2423
Abstract
Osteosarcoma (OS) is a type of bone cancer that is derived from primitive mesenchymal cells typically affecting children and young adults. The current standard of treatment is a combination of neoadjuvant chemotherapy and surgical resection of the cancerous bone. Post-resection challenges in bone [...] Read more.
Osteosarcoma (OS) is a type of bone cancer that is derived from primitive mesenchymal cells typically affecting children and young adults. The current standard of treatment is a combination of neoadjuvant chemotherapy and surgical resection of the cancerous bone. Post-resection challenges in bone regeneration arise. To determine the appropriate amount of bone to be removed, preoperative imaging techniques such as bone and CT scans are employed. To prevent local recurrence, the current standard of care suggests maintaining bony and soft tissue margins from 3 to 7 cm beyond the tumor. The amount of bone removed in an OS patient leaves too large of a deficit for bone to form on its own and requires reconstruction with metal implants or allografts. Both methods require the bone to heal, either to the implant or across the allograft junction, often in the setting of marrow-killing chemotherapy. Therefore, the issue of bone regeneration within the surgically resected margins remains an important challenge for the patient, family, and treating providers. Mesenchymal stem/stromal cells (MSCs) are potential agents for enhancing bone regeneration post tumor resection. MSCs, used with scaffolds and growth factors, show promise in fostering bone regeneration in OS cases. We spotlight two MSC types—bone marrow-derived (BM-MSCs) and adipose tissue-derived (ASCs)—highlighting their bone regrowth facilitation and immunomodulatory effects on immune cells like macrophages and T cells, enhancing therapeutic outcomes. The objective of this review is two-fold: review work demonstrating any ability of MSCs to target the deranged immune system in the OS microenvironment, and synthesize the available literature on the use of MSCs as a therapeutic option for stimulating bone regrowth in OS patients post bone resection. When it comes to repairing bone defects, both MB-MSCs and ASCs hold great potential for stimulating bone regeneration. Research has showcased their effectiveness in reconstructing bone defects while maintaining a non-tumorigenic role following wide resection of bone tumors, underscoring their capability to enhance bone healing and regeneration following tumor excisions. Full article
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