Diversity and homogeneity within endplates associated with physiologically identified static gamma-axons in cat tenuissimus muscle.

The terminations of static gamma-axons on chain fibres may be associated with a muscle surface contour thrown into complex folds at one extreme, ranging through lesser degrees of folding to being apparently uninfluenced by the presence of the terminals. The folding is not necessarily confined to the postsynaptic membrane. As a quantitative indicator of the degree of folding seen in cross-sections, the perimeters of the two halves of the intrafusal fibre with, and without the ending were compared. Both complexity of endplate structure and an undifferentiated appearance could co-exist within individual endings (of six static gamma-axons on thirteen chain fibres), associated with axons that supplied only chain fibres in the spindle isolated. (It should be noted, however, that the type of intrafusal fibres innervated by a particular axon was definitively identified only for the spindle isolated.) Endings of three other static gamma-axons on six chain fibres had a more homogeneous and less complex endplate structure; these supplied bag2 fibres in addition to the chain fibres and their endplates on the bag2 fibres were less folded than those of three axons which supplied bag2 fibres only. A sensory inhibitory influence on folding was not apparent because complexly folded endplates on chain fibres lay close (less than 500 microns) to sensory endings. All the endings studied were functional. In our experimental conditions all nine static gamma-axons which innervated chain fibres, alone, or together with a bag2 fibre, drove the Ia afferent at some stimulus frequencies; none of the three static gamma-axons innervating bag2 fibres alone caused driving at any frequency. These findings are discussed in relation to the concept of a dynamic remodelling of ending structure during life, to the relationship between the motor axon and the intrafusal fibre it innervates, and to the possibility that subgroups of static gamma-motoneurones might exist which could release different amounts of the trophic substances responsible for moulding the endplate structure.

The selectivity of fusimotor innervation in muscle spindles of the rat studied by light microscopy.

Six muscle spindles and three muscle spindle poles from four rat soleus muscles have been sectioned serially at 1 micron intervals to trace the motor innervation by light microscopy. Forty myelinated axons had 92 endings on the intrafusal muscle fibres. 67.5% of these axons supplied a single type of muscle fibre only, 22.5% to dynamic bag1 (Db1) fibres, 15% to static bag2 (Sb2) fibres and 30% to chain fibres. The rest supplied more than one fibre type, 5% supplying the Db1 and one chain fibre, 20% supplying the Sb2 and chain fibres, but 7.5% (three axons) supplied all the fibre types together. Apart from these three axons all the fusimotor axons would be expected to have a clear dynamic or static action on the Group Ia discharge. Whilst for the cat entirely non-specific distribution does not exist, or at least is very rare, since only a small proportion of the rat fusimotor axons were in this category we conclude that fusimotor distribution in rats and cats is essentially similar.

The ultrastructure of cat fusimotor endings and their relationship to foci of sarcomere convergence in intrafusal fibres.

1. Six muscle spindle poles, five from experiments in which foci of sarcomere convergence had been observed during stimulation of fusimotor axons, were serially sectioned for light and electron microscopy. Every somatic motor terminal was studied in ultrathin sections at several levels.2. In all six poles static gamma axons, or presumed static gamma axons, supplying the static bag(2) fibre and/or chain fibres had no terminations on the dynamic bag(1) fibre. In five poles, the dynamic bag(1) fibre was selectively innervated by dynamic gamma or beta axons save in one case where a dynamic gamma axon also innervated one chain fibre.3. Seventy-seven motor endings were of four distinct ultrastructural types: ;m(a) plates' lay superficially on the surface of static bag(2) or chain fibres; ;m(b) plates' were deeply indented into dynamic bag(1) fibres; in ;m(c) plates', found on chain fibres only, the muscle surface was thrown into projecting fingers between which the axon terminals were embedded; one type ;m(d) plate' was found, fully indented into a long chain fibre. A few plates of intermediate form (m(ab)) were variants of m(a) and m(b) plates.4. The muscle membrane beneath both m(a) and m(b) plates was smooth, or had a few wide, shallow folds; m(c) plates usually had wide, shallow subjunctional folds; numerous deep, narrow folds were characteristic of the m(d) plate. The length of unmyelinated pre-terminal axon or the number of sole plate nuclei were not useful diagnostic features.5. Obvious foci of sarcomere convergence in the capsular sleeve region of dynamic bag(1) and static bag(2) fibres coincided with the location of motor plates. Additional contraction foci were observed in the extracapsular region of dynamic bag(1) fibres where there was no motor innervation; contraction occurs principally in the outer half of these fibres. No foci of contraction or motor plates were observed in the extracapsular region of static bag(2) fibres; contraction in these fibres is typically mid-polar.6. In some poles local contraction of chain fibres centred on the location of m(c) plates. In others, very localized contraction occurred distal to the sites of m(a) plates. Both m(a) and m(c) plates were never found on the same pole of a chain fibre.7. Dynamic gamma or beta axons end in m(b) plates, probably equivalent to p(2) plates. The concept of distinctly different p(1) and p(2) plates on dynamic bag(1) fibres, supplied by dynamic beta and gamma axons, respectively, is not supported by ultrastructural evidence.8. Some static gamma axons end in multiple m(a) plates which correspond with ;trail endings', or in single large m(a) plates, on static bag(2) or chain fibres. The m(c) plates are the terminations of other static gamma, or occasionally dynamic gamma, axons on chain fibres. Static beta axons probably end in m(d) plates on long chain fibres which may correspond with p(1) plates.9. It is proposed that there are two types of static gamma motoneurone, one terminating in m(a) plates and the other in m(c) plates, possibly directed preferentially towards static bag(2) fibres and chain fibres, respectively.

Differential cell counts in the histiocytic variant of lymphocytic predominance subtype of Hodgkin's disease.

Differential cell counts were made on a lymph node, the structure of which was replaced by the histiocytic variant of the lymphocytic predominance subtype of diffuse Hodgkin's disease. In terms of numbers of cells in various categories, this lymph node bears a closer relationship to the mixed cellularity subtype than to the classical lymphocytic predominance subtype. In this node, unlike the mixed cellularity subtype, the histiocytes are largely differentiated into epithelioid cells; the significance of this cellular adaptation for defence against neoplastic cells is not known.

Cytological basis of histological typing of diffuse Hodgkin's disease. Demonstration of an implied misnomer in the terminology of the Rye classification.

Differential cell counts were made on nine lymph nodes whose structure was replaced by diffuse Hodgkin's disease; two of these nodes had the classical histological appearance of the lymphocytic predominance subtype, four of the mixed cellularity subtype, and three of the lymphocytic depletion subtype. Our attempts to achieve valid sampling methods are recorded. The counts, in general, confirm the postulated histological basis of the Rye classification of the subtypes of the diffuse disease. The major discrepancy is that, contrary to the histological descriptions, our direct counts have shown that lymphocytes, are, in general, more numerous in the lymphocytic depletion than in the mixed cellularity subtypes. The cell counts also show that normal mononuclear cells (mainly fibroblasts and macrophage-type cells) are much more numerous in the mixed cellularity subtype than in the other forms of diffuse Hodgkin's disease; this feature has not been emphasised in the Rye classification. On the basis of our differential counts, a hypothesis is proposed that could explain the natural history of the different subtypes of diffuse Hodgkin's disease as the resultant of three processes: (a) tumour aggressiveness, (b) specific cell-mediated immunological reactions, and (c) non-immunological stromal responses.