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1.
Glia ; 56(16): 1791-8, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18649405

ABSTRACT

Gap junctions are intercellular channels formed by hemichannels (or connexons) from two neighboring cells. Hemichannels, which are composed of proteins called connexins, can function as conduits of ATP and glutamate, and interact with adhesion molecules and other signaling elements. As a result, their functional repertoire is expanding into other roles, such as control of cell growth or cell migration. Here we further elucidate the involvement of hemichannels in cell-cell adhesion by analyzing how connexins regulate cell adhesion without the need of gap junction formation. Using a short-term aggregation assay with C6-glioma and HeLa cells stably transfected with connexin (Cx) 43 or Cx32, we found that the connexin type dictates the ability of these cells to aggregate, even though these two cell types do not usually adhere to each other. We have also found that high expression of Cx43, but not Cx32 hemichannels, can drive adhesion of cells expressing low levels of Cx43. Aggregation was not dependent on high levels of extracellular Ca(2+), as Ca(2+) removal did not change the aggregation of Cx43-expressing cells. Our data confirm that connexin hemichannels can establish adhesive interactions without the need for functional gap junctions, and support the concept that connexins act as adhesion molecules independently of channel formation.


Subject(s)
Brain/metabolism , Connexin 43/metabolism , Gap Junctions/metabolism , Neurons/metabolism , Animals , Brain/ultrastructure , Calcium Channels/metabolism , Calcium Signaling/physiology , Cell Adhesion/physiology , Cell Communication/physiology , Cell Line, Tumor , Connexins/metabolism , Gap Junctions/ultrastructure , Humans , Mice , Neurons/ultrastructure , Gap Junction beta-1 Protein
2.
J Bone Joint Surg Br ; 86(7): 1072-6, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15446542

ABSTRACT

The healing of a hamstring graft to bone is the weak link in the reconstruction of a cruciate ligament using this donor material. We therefore investigated the augmentation of healing at the tendon-bone interface using calcium-phosphate cement (CPC). We performed semitendinosus autograft reconstructions of the anterior cruciate ligament on both knees of 22 New Zealand white rabbits. The interface between the grafted tendon and the bone tunnel for one knee was filled with CPC. Six rabbits were killed at the end of the first and second post-operative weeks in order to evaluate the biomechanical changes. Two rabbits were then killed sequentially at the end of weeks 1, 3, 6, 12 and 24 after operation and tissue removed for serial histological observation. Histological examination showed that the use of CPC produced early, diffuse and massive bone ingrowth. By contrast, in the non-CPC group of rabbits only a thin layer of new bone was seen. Mechanical pull-out testing at one week showed that the mean maximal tensile strength was 6.505 +/- 1.333 N for the CPC group and 2.048 +/- 0.950 N for the non-CPC group. At two weeks the values were 11.491 +/- 2.865 N and 5.452 +/- 3.955 N, respectively. Our findings indicate that CPC is a potentially promising material in clinical practice as regards its ability to reinforce the fixation of the tendon attachment to bone and to augment the overall effectiveness of tendon healing to bone.


Subject(s)
Anterior Cruciate Ligament/surgery , Bone Cements/pharmacology , Calcium Phosphates/pharmacology , Tendons/transplantation , Wound Healing/drug effects , Animals , Anterior Cruciate Ligament Injuries , Femur/pathology , Femur/surgery , Graft Survival , Male , Rabbits , Tensile Strength
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