Fibrinogen αC-subregions critically contribute blood clot fibre growth, mechanical stability and resistance to fibrinolysis

Fibrinogen is essential for blood coagulation. The C-terminus of the fibrinogen α-chain (αC-region) is composed of an αC-domain and αC-connector. Two recombinant fibrinogen variants (α390 and α220) were produced to investigate the role of subregions in modulating clot stability and resistance to lysis. The α390 variant, truncated before the αC-domain, produced clots with a denser structure and thinner fibres. In contrast, the α220 variant, truncated at the start of the αC-connector, produced clots that were porous with short, stunted fibres and visible fibre ends. These clots were mechanically weak and susceptible to lysis. Our data demonstrate differential effects for the αC-subregions in fibrin polymerisation, clot mechanical strength, and fibrinolytic susceptibility. Furthermore, we demonstrate that the αC-subregions are key for promoting longitudinal fibre growth. Together, these findings highlight critical functions of the αC-subregions in relation to clot structure and stability, with future implications for development of novel therapeutics for thrombosis.

Fibrinogen αC-subregions critically contribute blood clot fibre growth, mechanical stability and resistance to fibrinolysis

Fibrinogen is essential for blood coagulation. The C-terminus of the fibrinogen α-chain (αC-region) is composed of an αC-domain and αC-connector. Two recombinant fibrinogen variants (α390 and α220) were produced to investigate the role of subregions in modulating clot stability and resistance to lysis. The α390 variant, truncated before the αC-domain, produced clots with a denser structure and thinner fibres. In contrast, the α220 variant, truncated at the start of the αC-connector, produced clots that were porous with short stunted fibres and visible fibre ends. These clots were mechanically weak and susceptible to lysis. Our data demonstrate differential effects for the αC-subregions in fibrin polymerisation, clot mechanical strength, and fibrinolytic susceptibility. Furthermore, we demonstrate that the αC-subregions are key for promoting longitudinal fibre growth. Together, these findings highlight critical functions of the αC-subregions in relation to clot structure and stability, with future implications for development of novel therapeutics for thrombosis.

Pressurised compressive chip pre-treatment of Norway spruce with a mill scale Impressafiner

Mill scale trials were performed to evaluate pressurised compressive chip pre-treatment with the Impressafiner installed in one of the thermomechanical pulp lines at Braviken paper mill (Holmen Paper AB). The aim of the study was to determine if earlier reported effects of the Impressafiner pre-treatment on spruce chips from pilot scale trials (i.e. energy reduction and extractives removal) could also be attained with the mill scale Impressafiner. The mill scale Impressafiner pre-treatment resulted in partial disintegration of chips into a material consisting of fragmented chips with cracks running along the longitudinal fibre axis. Splits or evidence for weaknesses were observed between the primary and secondary fibre walls of pre-treated chips. An increase in water uptake for pre-treated chips was also observed. The extractive content was reduced by up to 24% for pulps produced with pre-treated chips compared to pulps from untreated chips. Pulp produced from pre-treated chips had higher tensile- and tear indices, elongation and light scattering and lower freeness compared to pulps from untreated chips produced with the same total specific energy consumption. The total specific energy needed to reach a tensile index of 47 Nm/g was reduced by 120 kWh/bone dry ton (6%) with Impressafiner pre-treatment. A smaller refiner plate gap was needed to reach the same specific energy consumption for pre-treated chips compared to untreated chips.

Contraction dynamics and power production of pink muscle of the scup (Stenotomus chrysops).

Although the contribution of red muscle to sustained swimming in fish has been studied in detail in recent years, the role of pink myotomal muscle has not received attention. Pink myotomal muscle in the scup (Stenotomus chrysops) lies just medial to red muscle, has the same longitudinal fibre orientation and is recruited along with the red muscle during steady sustainable swimming. However, pink muscle has significantly faster rates of relaxation, and the maximum velocity of shortening of pink muscle (7.26 +/- 0.18 muscle lengths s-1, N = 9, at 20 degrees C, and 4.46 +/- 0.15 muscle lengths s-1, N = 6, at 10 degrees C; mean +/- S.E.M.) is significantly faster than that of red muscle. These properties facilitate higher mass-specific maximum oscillatory power production relative to that of red muscle at frequencies similar to the tailbeat frequency at maximum sustained swimming speeds in scup. Additionally, pink muscle is found in anatomical positions in which red muscle is produces very little power during swimming: the anterior region of the fish, which undergoes the lowest strain during swimming. Pink muscle produces more oscillatory power than red muscle under low-strain conditions (+/- 2-3%) and this may allow pink muscle to supplement the relatively low power generated by red muscle in the anterior regions of swimming scup.

Serotonin immunoreactivity in the ventral nerve cord of the primitive crustacean Anaspides tasmaniae closely resembles that of crayfish

Syncarid crustaceans, of which only a few living species remain, have articulated segments with well-developed appendages along the length of the body, an arrangement thought to resemble that of the earliest malacostracan crustaceans. Decapod malacostracans have fused thoracic segments and reduced abdominal appendages. Modern representatives of the two groups are separated by at least 300 million years of evolutionary history. The serotonin immunoreactivity of ganglia and connectives from the ventral nerve cord of the syncarid Anaspides tasmaniae was compared with that of serially homologous ganglia of the crayfish Cherax destructor. Both species show the serotonin-immunoreactive longitudinal fibre bundles described from other decapods and thought to be part of a neuromodulatory network. They also have in common a number of the cell bodies associated with this system. Each species has some serotonergic cells in the region examined that are not present, or that do not stain, in the other species.

Cholinergic Innervation of Muscle Fibres in Squid

INTRODUCTIONThe small squid Alloteuthis, and the larger Loligo have elongate mantles chiefly made up of two distinct types of circular muscle fibres, partitioned by thin sheets of radial muscle fibres (Bone, Pulsford & Chubb, 1981).Nerve terminals on both types of circular fibre and upon radial fibres contain 50 nm electron-lucent vesicles; preliminary pharmacological investigations (Bone & Howarth, 1980) indicate that L-glutamate is the excitatory transmitter at the terminals upon the circular fibres. In other cephalopods, such as Sepia, and the squids Lepidoteuthis and Taningia (Clarke & Maul, 1962; Clarke, 1967) there are in addition to the circular and radial fibres, layers of longitudinal muscle fibres in the mantle. Such longitudinal fibre layers are lacking over the greater part of the mantle in Alloteuthis and Loligo. In this note, we show that they are present only around the anterior margin of the mantle in these two squid, and that both these anterior longitudinal fibres and the radial fibres of the mantle are insensitive to L-glutamate, but contract in response to acetylcholine, as do the retractor muscles of the head and arms, and the siphon muscles.

The structure of the ventral nerve cord of Caenorhabditis elegans

The nervous system of Caenorhabditis elegans is arranged as a series of fibre bundles which run along internal hypodermal ridges. Most of the sensory integration takes place in a ring of nerve fibres which is wrapped round the pharynx in the head. The body muscles in the head are innervated by motor neurones in this nerve ring while those in the lower part of the body are innervated by a set of motor neurones in a longitudinal fibre bundle which joins the nerve ring, the ventral cord. These motor neurones can be put into five classes on the basis of their morphology and synaptic input. At any one point along the cord only one member from each class has neuromuscular junctions. Members of a given class are arranged in a regular linear sequence in the cord and have non-overlapping fields of motor synaptic activity, the transition between fields of adjacent neurones being sharp and well defined. Members of a given class form gap junctions with neighbouring members of the same class but never to motor neurones of another class. Three of the motor neurone classes receive their synaptic input from a set of interneurones coming from the nerve ring. These interneurones can in turn be grouped into four classes and each of the three motor neurone classes receives its synaptic input from a unique combination of interneurone classes. The possible developmental and functional significance of these observations is discussed.