Search PubMedSearch

PubMed · 991514

Bone morphogenesis and surface charge.

Abstract

The electrophoretic mobility of variously treated bone specimens, with and without bone morphogenetic activity, has been measured in physiological solutions. The Bone Morphogenetic Principle appears to be associated with a minimum negative surface charge on the implant that corresponds to that of normal undemineralized cortical bone in saline. Demineralization of cortical bone in 0.6 N HCI at 2 degrees consistently increases the bone negative surface charge, and biologically produces an implant with morphogenetic activity. It is suggested that through the mediation of the positively charges ionic layer surrounding the negative implant that the negatively charged mesenchymal cell is able to reside in very close contact with the surfaces of the implant. The binding force can be expected to be directly proportional to the degree of negativity of the implant. However, implants with a positive zeta potentaial will be surrounded by ions with a net negative charge so discouraging the stable positioning of mesenchymal cells in close contact with the implant. The negative surface charge corresponding to that of untreated cortical bone is apparently borderline in permitting such a close contact for a sufficiently long period of time for differentiation to follow.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

C Eriksson. Bone morphogenesis and surface charge.. https://pubmed.ncbi.nlm.nih.gov/991514/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Trabecular generation de novo. A morphological and immunohistochemical study of primary ossification in the human femoral anlagen.

An understanding of trabecular formation in early skeletal development may provide insight into the problem of trabecular replacement in the aging skeleton. In an optical and scanning electron microscope study of the processes of de novo trabecular generation, the immunohistochemical distribution of collagen Types I, II and III, together with the matrix organising proteins fibronectin and tenascin, has been examined in the ossifying human femoral anlage. In the region of the developing spongiosa, the primary osseous trabeculae that arose by endochondral ossification were assembled around calcified cartilage remnants, consisting almost entirely of aggregates of mineralised microspheres. These structures were specifically recognised by antibodies raised against collagen Type II and fibronectin. In contrast, the primary osseous trabeculae that arose by subperiosteal intramembranous processes, were assembled around a framework of prominent coarse fibres that were recognised by antibodies raised against collagen Type III and tenascin. Irrespective of their origin, all the new trabeculae were similar in their general staining character for collagen Type I and fibronectin. However, throughout the developmental stages examined here endochondral trabeculae were separated from intramembranous trabeculae by a discrete boundary of compressed cells and mineralised cartilage.

Bone Development

The periphysis and its effect on the metaphysis: I. Definition and normal radiographic pattern.

The zone of Ranvier and the ring of LaCroix, together with the membranous bone bark they produce, are termed the periphysis in order to emphasize their normal effect (the metaphyseal collar) on the metaphysis of the infant and young child. In the first 7 years of life, the normal collar at the wrist is 1-3 mm wide. The step-off between the metaphyseal collar and the curvilinear metaphysis, at the margin of the periphysis, should not be mistaken for abuse fracture. The periphyseal bone bark may be radiologically visible at the edge of the physis at the distal ulna in 9% of infants and should not be mistaken for fracture or rickets.

Bone Development

Radiological assessment of the effects of splinting on early hip development: results from a randomised controlled trial of abduction splinting vs sonographic surveillance.

Whilst delayed treatment of fully dislocated hips diagnosed at birth prejudices final outcome, splinting clinically dislocatable hips is controversial as the majority stabilise spontaneously. Early stabilisation may not ensure normal development but even early splinting carries a small risk of avascular necrosis. We report radiological data from 76 newborns with dislocatable hips that were randomised either to immediate splinting or to sonographic surveillance which examines the influence of early splinting on hip development. Epiphyseal maturation (EM), iliac indentation (II) and acetabular angle (AA) were assessed radiographically at 6 months, blind to the treatment group; hips with normal sonograms at birth had greater EM and II and smaller AA. Whilst clinically unstable Graf type 1 and 2A hips were radiologically similar at 6 months, those splinted showed poorer EM and II compared with non-splinted hips. There were no cases of avascular necrosis. Abduction splinting may displace the femoral capital epiphysis medially resulting in poorer iliac indentation. The smaller epiphysis in splinted infants may be secondary to altered blood supply due to increased pressure between the femoral head and acetabulum and increased tension of the adductor muscles in the thigh. These differences were less marked by 1 year. Whether they have any long-term significance requires further study.

Bone Development