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A Martínez-Almagro

Publications and source records attributed to A Martínez-Almagro.

2 recordsLinked to original sources

S100alpha and S100beta proteins in human cutaneous sensory corpuscles: effects of nerve and spinal cord injury.

S100 protein in the vertebrate peripheral nervous system consists of homo- or heterodimers of S100alpha and S100beta proteins, the first predominating in neurons and the second in glial cells. Recently, however, occurrence of S100beta protein in neurons has been reported. The expression of S100 protein by Schwann cells, as well as their derivatives in sensory corpuscles, depends on the sensory axon (i.e., the Schwann cell-axon contact). The present study analyzed the distribution of S100alpha and S100beta proteins in human cutaneous sensory corpuscles and the effects of peripheral or central sensory axon severance in the expression of these proteins. Simple or double immunohistochemistry was carried out using a panel of antibodies against S100alpha, S100beta or S100alpha+beta proteins, and the sections were examined by light or laser confocal scanning microscopy. Skin samples were obtained from normal subjects and patients with spinal cord injury, nerve entrapment, and nerve sections plus graft. The lamellar cells of Meissner corpuscles as well as the inner-core lamellae of the Pacinian corpuscles displayed strong immunoreactivity (IR) for all antigens examined, the most intense labeling being obtained for S100beta protein. The pattern of immunostaining was unchanged after spinal cord injury, whereas the number of stained corpuscles as well as the intensity of IR for each antigen decreased in cutaneous sensory corpuscles after nerve injury, both entrapment and section plus graft. No evidence was found of axonal labeling. The present results provide evidence that Schwann-related cells in human cutaneous sensory corpuscles contain both S100alpha and S100beta and that the expression of these proteins is dependent on the functional and structural integrity of sensory fibers.

Adult↗

Pregnancy-induced denervation of the human uterine artery correlates with local decrease of NGF and TrkA.

Pregnancy induces transient and reversible denervation of the mammalian uterus and uterine artery which origin remains still unclear. It is well established that the density of sympathetic innervation is regulated by the levels of peptidergic diffusible growth factors, especially nerve growth factor (NGF). Whether a decrease of NGF and/or its signal-transducing receptor TrkA are involved in this physiological denervation of the uterine artery during pregnancy has not been analyzed. The aim of the present study is to analyze this topic on human uterine artery using ELISA, Western blotting and immunohistochemistry (associated to quantitative image analysis). The material was obtained from surgical pieces (hysterectomy) of non-pregnant and pregnant women from 4 to 16 weeks of gestation. The density of innervation for tyrosine hydroxylase assessed in whole mount samples of uterine artery, as well as the density of nerve fibers identified with other general nerve (PGP 9.5 and NFP) or Schwann cell (S-100 protein) markers was significantly reduced (p<0.05) in the uterine artery from pregnant woman. On the other hand, the tissular levels of NGF, the density of TrkA, and the immunostaining for both NGF and TrkA, were significantly reduced in uterine arteries from pregnant patients. These results strongly suggest that the physiological denervation occurring in the uterine artery during pregnancy is related to a decrease in the availability of NGF by nerve fibers, and to the impossibility to mediate its effect due to a remarkable decrease in the signal-transducing TrkA receptor.

Adult↗