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<dc:contributor>García-Sancho Martín, Francisco Javier</dc:contributor>
<dc:contributor>Alonso Alonso, María Teresa</dc:contributor>
<dc:contributor>Universidad de Valladolid. Facultad de Medicina</dc:contributor>
<dc:creator>Río Lorenzo, Alba del</dc:creator>
<dc:date>2020</dc:date>
<dc:description>Aging still remains a mystery of biology and one of the most affected tissues in&#xd;
aging is skeletal muscle, whose loss of muscle mass and strength is called&#xd;
sarcopenia. Age-dependent sarcopenia is not restricted to mammals, as it affects&#xd;
other animal species including nematodes or flies. Cytosolic Ca2+ ion is the&#xd;
intracellular second messenger that triggers muscle contraction. The sarcoplasmic&#xd;
reticulum is the store of Ca2+ in the muscle cell, and it releases Ca2+ to the cytosol&#xd;
when muscle contracts. Sarcopenia has been linked to the loss of Ca2+&#xd;
homeostasis that trigger muscle contraction, but mechanistic details remain&#xd;
unsolved.&#xd;
Here we explore the hypothesis that an alteration of the Ca2+ content within the&#xd;
sarcoplasmic reticulum (SR) is at the origin of this loss of Ca2+ homeostasis&#xd;
observed in sarcopenia. For investigating this hypothesis, we generated transgenic&#xd;
flies that express the ratiometric low affinity Ca2+ indicator GAP3 targeted to the&#xd;
muscle sarcoplasmic reticulum (erGAP3), and we developed a new method to&#xd;
calibrate erGAP3 fluorescent signals into SR/ER Ca2+ concentrations ([Ca2+]SR/ER).&#xd;
With these tools we measured resting [Ca2+]SR in vivo along the fly life, and found&#xd;
a progressive decrease with aging that results in a tenfold reduction in the [Ca2+]SR&#xd;
in the oldest flies. Then, to explore the molecular mechanisms involved in this&#xd;
decrease of [Ca2+]SR we studied the expression levels of the main proteins involved&#xd;
in [Ca2+]SR resting levels. In old muscle, we found a slight non-significant increase&#xd;
in the ryanodine receptors (RyR) and in the immunoglobulin protein (BiP)&#xd;
expression whereas the expression of the sarco/endoplasmic reticulum Ca2+-&#xd;
ATPase (SERCA) decreased by 35%. Moreover, the loss of function of the skeletal&#xd;
muscle was monitored by the well-characterized climbing assay, and found a&#xd;
strong correlation between the Ca2+ content of the sarcoplasmic reticulum and fly&#xd;
climbing ability with aging. Furthermore, to assess whether the reduction of&#xd;
[Ca2+]SR content in the aged flies also affected the [Ca2+]C transients, we studied&#xd;
the cytosolic Ca2+ dynamics during muscle contraction in transgenic flies&#xd;
expressing the cytosolic Ca2+ sensor GCaMP in the muscle tissue. This&#xd;
experiments showed that old flies released less Ca2+ to the cytosol in comparison&#xd;
to young flies and, thus, these results validated those obtained in the SR.&#xd;
In order to investigate whether the reduction of SR Ca2+ content observed in&#xd;
muscle was a universal phenomenon of aging that occurred also in other tissues we studied the progression of [Ca2+]ER in brain neurons and in the peripheral&#xd;
sensory wing neurons using the pan neuronal transgenic line, which expresses&#xd;
erGAP3 in all types of neurons. The [Ca2+]ER of the brain neurons did not change&#xd;
significantly with age, and remained stable along the whole fly life. However, the&#xd;
behaviour is different in other neurons as we can also appreciate a decrease in the&#xd;
[Ca2+]ER of the sensory wing neurons, similar to what occurs in the skeletal muscle.&#xd;
Regarding the key molecular players, in contrast to the muscle, SERCA levels&#xd;
remained unchanged in brain neurons whereas BiP and RyR levels are increased&#xd;
in the aging brain.</dc:description>
<dc:format>application/pdf</dc:format>
<dc:identifier>http://uvadoc.uva.es/handle/10324/43643</dc:identifier>
<dc:language>eng</dc:language>
<dc:subject>Calcio</dc:subject>
<dc:subject>Sarcopenia</dc:subject>
<dc:subject>32 Ciencias Médicas</dc:subject>
<dc:title>Sarcoplasmic reticulum Ca2+ dynamics in aging Drosophila and correlation with sarcopenia</dc:title>
<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
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