Abstract:Albumin is a major plasma protein that has become ubiquitous in regenerative medicine research. As such, many studies have examined its structure and advantageous properties. However, a systematic and comprehensive understanding of albumin's role, capabilities and therapeutic potential still eludes the field. In the present work, we review how albumin is applied in tissue engineering, including cell culture and storage, in vitro fertilization and transplantation. Furthermore, we discuss how albumin's physiolog… Show more
“…With this in mind, the authors showed that serum albumin‐coated bone allograft (BoneAlbumin) successfully supports bone regeneration in various experimental models. The idea behind the phenomenon is that locally increased albumin concentration induces endogenous progenitor recruitment, resulting in the presence of a higher cell number to support the tissue remodelling phase (Horvathy, Simon, et al, ). Evidence of stem cell activation was supported by a first‐in‐human investigation, in which large albumin‐coated structural allografts were used to support recovery after total joint revision arthroplasty, with single photon emission computed tomography (SPECT) analysis showing increased osteoblast activation even 1 year after operation (Klara, Csonge, Janositz, Csernatony, & Lacza, ).…”
Section: Discussionmentioning
confidence: 99%
“…BoneAlbumin was also shown to decrease donor site morbidity and enhance bone formation after anterior cruciate ligament reconstruction with bone‐patellar tendon‐bone autografts (Schandl et al, ). Moreover, in a thorough review article, the albumin molecule was shown to have an important and potentially active but not yet completely understood role in bone regeneration (Horvathy, Simon, et al, ). Additionally, stem cell function was tested on various serum albumin‐coated surfaces.…”
Serum albumin‐coated bone allografts (BoneAlbumin) have successfully supported bone regeneration in various experimental models by activating endogenous progenitors. However, the effect of tissue aging, linked to declining stem cell function, has yet to be explicitly examined within the context of BoneAlbumin's regenerative capacity. Stem cell function was tested with an in vitro attachment assay, which showed that albumin coating increases stem cell attachment on demineralized bone surfaces in an aging cell population. Bone regeneration was investigated in vivo by creating critical size bone defects on the parietal bones of aging female rats. Demineralized bone matrices with and without serum albumin coating were used to fill the defects. Bone regeneration was determined by measuring the density and the size of the remaining bone defect with computed tomography (CT). Microcomputed tomography (MicroCT) and mechanical testing were performed on the parietal bone explants. In vivo CT and ex vivo microCT measurements showed better regeneration with albumin‐coated grafts. Additionally, the albumin‐coated group showed a twofold increase in peak fracture force compared with uncoated allografts. In the present study, serum albumin‐coated demineralized bone matrices successfully supported faster and functionally superior bone regeneration in aging rats. Because stem cell function, a key contributor of bone remodelling, decreases with age and serum albumin is an effective activator of endogenous progenitor cells, this method could be an effective and safe adjuvant in bone regeneration of aging adult and osteo‐compromised populations.
“…With this in mind, the authors showed that serum albumin‐coated bone allograft (BoneAlbumin) successfully supports bone regeneration in various experimental models. The idea behind the phenomenon is that locally increased albumin concentration induces endogenous progenitor recruitment, resulting in the presence of a higher cell number to support the tissue remodelling phase (Horvathy, Simon, et al, ). Evidence of stem cell activation was supported by a first‐in‐human investigation, in which large albumin‐coated structural allografts were used to support recovery after total joint revision arthroplasty, with single photon emission computed tomography (SPECT) analysis showing increased osteoblast activation even 1 year after operation (Klara, Csonge, Janositz, Csernatony, & Lacza, ).…”
Section: Discussionmentioning
confidence: 99%
“…BoneAlbumin was also shown to decrease donor site morbidity and enhance bone formation after anterior cruciate ligament reconstruction with bone‐patellar tendon‐bone autografts (Schandl et al, ). Moreover, in a thorough review article, the albumin molecule was shown to have an important and potentially active but not yet completely understood role in bone regeneration (Horvathy, Simon, et al, ). Additionally, stem cell function was tested on various serum albumin‐coated surfaces.…”
Serum albumin‐coated bone allografts (BoneAlbumin) have successfully supported bone regeneration in various experimental models by activating endogenous progenitors. However, the effect of tissue aging, linked to declining stem cell function, has yet to be explicitly examined within the context of BoneAlbumin's regenerative capacity. Stem cell function was tested with an in vitro attachment assay, which showed that albumin coating increases stem cell attachment on demineralized bone surfaces in an aging cell population. Bone regeneration was investigated in vivo by creating critical size bone defects on the parietal bones of aging female rats. Demineralized bone matrices with and without serum albumin coating were used to fill the defects. Bone regeneration was determined by measuring the density and the size of the remaining bone defect with computed tomography (CT). Microcomputed tomography (MicroCT) and mechanical testing were performed on the parietal bone explants. In vivo CT and ex vivo microCT measurements showed better regeneration with albumin‐coated grafts. Additionally, the albumin‐coated group showed a twofold increase in peak fracture force compared with uncoated allografts. In the present study, serum albumin‐coated demineralized bone matrices successfully supported faster and functionally superior bone regeneration in aging rats. Because stem cell function, a key contributor of bone remodelling, decreases with age and serum albumin is an effective activator of endogenous progenitor cells, this method could be an effective and safe adjuvant in bone regeneration of aging adult and osteo‐compromised populations.
“…Thus, it is an advantageous preparation method to help in the application of an autologous biocompatible membrane for tissue regeneration. In the following experimental steps this membrane can be useful to start clinical studies to investigate the effect of frozen hypACT PRF membrane as gingival graft after bone replacing by albumin-coated bone granules in maxillofacial surgery [ 42 , 43 , 44 , 45 ], the material is also a promising candidate for clininal studies in orthopedics, namely in cartilage regeneration.…”
Platelet-rich fibrin (PRF) membrane is a three-dimensional biodegradable biopolymer, which consists of platelet derived growth factors enhancing cell adhesion and proliferation. It is widely used in soft and hard tissue regeneration, however, there are unresolved problems with its clinical application. Its preparation needs open handling of the membranes, it degrades easily, and it has a low tensile strength which does not hold a suture blocking wider clinical applications of PRF. Our aim was to produce a sterile, suturable, reproducible PRF membrane suitable for surgical intervention. We compared the biological and mechanical properties of PRF membranes created by the classical glass-tube and those that were created in a single-syringe closed system (hypACT Inject), which allowed aseptic preparation. HypACT Inject device produces a PRF membrane with better handling characteristics without compromising biological properties. Freeze-thawing resulted in significantly higher tensile strength and higher cell adhesion at a lower degradation rate of the membranes. Mesenchymal stem cells seeded onto PRF membranes readily proliferated on the surface of fresh, but even better on freeze/thawed or freeze-dried membranes. These data show that PRF membranes can be made sterile, more uniform and significantly stronger which makes it possible to use them as suturable surgical membranes.
“…However, it is unavoidable to supplement cell cultures with serum-specific growth factors, and other, still-unidentified factors of the serum as MSCs cannot survive in the absence of such components. Thus, human blood-derived additives like human serum albumin (HSA) [ 12 ] or platelet releasates such as platelet-rich plasma (PRP) are considered as efficient alternatives to replace FCS [ 13 , 14 ]. The scientific rationale behind platelet-rich products is that thrombocytes provide a diverse growth factor supply such as platelet-derived growth factors (PDGFs), transforming growth factor beta-1 (TGF β -1) or vascular endothelial growth factor (VEGF), coagulation factors, serotonin, mitogens, and adhesion factors like fibronectin, fibrin, or vitronectin to support healing [ 15 ].…”
Mesenchymal stem cells (MSCs) are widely used in laboratory experiments as well as in human cell therapy. Their culture requires animal sera like fetal calf serum (FCS) as essential supplementation; however, animal sera pose a risk for clinical applications. Human blood derivatives, for example, platelet-rich plasma (PRP) releasates, are potential replacements of FCS; however, it is unclear which serum variant has the best effect on the given cell or tissue type. Additionally, blood derivatives are commonly used in musculoskeletal diseases like osteoarthritis (OA) or osteonecrosis as “proliferative agents” for the topical MSC pool. Hyperacute serum (HAS), a new serum derivative, has been designed to approximate the natural coagulation cascade with a single-step, additive-free preparation method. We investigated the effects of HAS on monolayer MSC cultures and in their natural niche, in 3D subchondral bone and marrow explants. Viability measurements, RT-qPCR evaluation for gene expression and flow cytometry for cell surface marker analysis were performed to compare the effects of FCS-, PRP-, or HAS-supplemented culture media. Monolayer MSCs showed significantly higher metabolic activity following 5 days' incubation in HAS, and osteoblast-specific mRNA expression was markedly increased, while cells also retained their MSC-specific cell surface markers. A similar effect was observed on bone and marrow explants, which was further confirmed with confocal microscopy analysis. Moreover, markedly higher bone marrow preservation was observed with histology in case of HAS supplementation compared to FCS. These findings indicate possible application of HAS in regenerative solutions of skeletal diseases like OA or osteonecrosis.
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