A case of co-operative nursing and offspring care by mother and daughter feral horses

Among mammals, non-offspring nursing is the most extreme form of communal parenting. This is because lactation is the most energetically costly part of parental investment (Clutton-Brock, 1991; Packer, Lewis & Pusey, 1992). Non-offspring nursing is most common in species characterized by large litters and small kin groups (Packer et al ., 1992; e.g. lions Panthera leo : Pusey & Packer, 1994). Although non-offspring nursing has also been reported in monotocous species (e.g. water buffalo Bubalus bubalus , Murphey et al ., 1995; African elephant Loxodonta africana : Dublin, 1983; Lee, 1987; Indian elephant Elaphus maximus : MacKay, 1973; Rapaport & Haight, 1987; fallow deer Cervus dama : San José & Braza, 1993) it is almost always associated with reproductive errors (Riedman, 1982) such as milk theft or exclusive adoption (Packer et al ., 1992). However, simultaneous non-offspring nursing in monotocous species has been reported in some bat species (e.g. McCracken, 1984; Eales, Bullock & Slater, 1988), African elephants (Lee, 1987), and captive Indian elephants (Rapaport & Haight, 1987). Recent research, however, suggests that nutritive non-offspring nursing in African elephants is rarer than previously thought as most reported instances were probably non-lactating juveniles allowing infants to suckle (Lee & Moss, 1986; Lee, 1987, 1989).     

Multiple Forms and Distribution of Calcium/Calmodulin-Stimulated Protein Kinase II in Brain

In recent years, the enzyme Ca²⁺/calmodulin-stimulated protein kinase II¹ (CaM-PK II) as attracted a great deal of interest. CaM-PK II is the most abundant calmodulin-stimulated protein kinase in brain, where it is particularly enriched in neurons (Ouimet et al., 1984; Erondu and Kennedy, 1985; Lin et al., 1987; Scholz et al., 1988). Neuronal CaM-PK II has been suggested to be involved in several phenomena associated with synaptic plasticity (Lisman and Goldring, 1988; Kelly, 1992), including long-term potentiation (Malinow et al., 1988; Malenka et al.,1989), neurotransmission (Nichols et al., 1990; Siekevitz, 1991), and learning (for review, see Rostas, 1991). This enzyme has also been postulated to be selectively vulnerable in several pathological condition, including epilepsy/kindling (Bronstein et al.,1990; Wu et al., 1990), cerebral ischemia (Taft et al., 1988), and organophosphorus toxicity (Abou-Donia and Lapadula, 1990).     

Flow cytometric analysis of European flat oyster, Ostrea edulis, haemocytes using a monoclonal antibody specific for granulocytes

The importance of haemocytes in mollusc defence mechanisms can be inferred from their functions. They participate in pathogen elimination by phagocytosis (Cheng, 1981; Fisher, 1986). Hydrolytic enzymes and cytotoxic molecules produced by haemocytes contribute to the destruction of pathogenic organisms (Cheng, 1983; Leippe & Renwrantz, 1988; Charlet et al., 1996; Hubert et al., 1996; Roch et al., 1996). Haemocytes may also be involved in immunity modulation by the production of cytokines and neuropeptides (Hughes et al., 1990; Stefano et al., 1991; Ottaviani et al., 1996). As a result, the literature dealing with bivalve haemocyte studies has increased during the last two decades. Most of these publications use microscopy for morphological analysis (Seiler & Morse, 1988; Auffret, 1989; Hine & Wesney, 1994; Giamberini et al., 1996; Carballal et al., 1997; Lopez et al., 1997; Nakayama et al., 1997), and functional analysis (e.g. phagocytosis) (Hinsch & Hunte, 1990; Tripp, 1992; Mourton et al., 1992; Fryer & Bayne, 1996; Mortensen & Glette, 1996). Flow cytometry represents a rapid technique applicable to both morphological and functional studies of cells in suspension. While the measurements based on autofluorescence provide information on cell morphology, the analyses with fluorescent markers including labelled antibodies, offer data on phenotyping and cell functions. As a result, its application has greatly contributed to the investigation of immunocyte functions and differentiation in vertebrates (Stewart et al., 1986; Rothe & Valet, 1988; Ashmore et al., 1989; Koumans-van Diepen et al., 1994; Rombout et al., 1996; Caruso et al., 1997). Some authors studied oyster haemocyte populations by flow cytometry based on cellular autofluorescence (Friedl et al., 1988; Fisher & Ford, 1988; Ford et al., 1994). However, no analysis using specific monoclonal antibodies has been reported to date. In this study, a protocol for studying European flat oyster, Ostrea edulis, haemocytes by flow cytometry using a monoclonal antibody specific for granulocytes and an indirect immunofluorescence technique have been developed. European flat oysters, Ostrea edulis, 7-9 cm in shell length were obtained from shellfish farms in Marenne Oléron bay (Charente Maritime, France) on the French Atlantic coast. All individuals were purchased just before each experiment and processed without any previous treatment.     

CFTR: Domains, Structure, and Function

Mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) cause cystic fibrosis (CF) (Collins, 1992). Over 500 naturally occurring mutations have been identified in CF gene which are located in all of the domains of the protein (Kerem et al., 1990; Mercier et al., 1993; Ghanem et al., 1994; Fanen et al., 1992; Ferec et al., 1992; Cutting et al., 1990). Early studies by several investigators characterized CFTR as a chloride channel (Anderson et al.; 1991b,c; Bear et al., 1991). The complex secondary structure of the protein suggested that CFTR might possess other functions in addition to being a chloride channel. Studies have established that the CFTR functions not only as a chloride channel but is indeed a regulator of sodium channels (Stutts et al., 1995), outwardly rectifying chloride channels (ORCC) (Gray et al., 1989; Garber et al., 1992; Egan et al., 1992; Hwang et al., 1989; Schwiebert et al., 1995) and also the transport of ATP (Schwiebert et al., 1995; Reisin et al., 1994). This mini-review deals with the studies which elucidate the functions of the various domains of CFTR, namely the transmembrane domains, TMD1 and TMD2, the two cytoplasmic nucleotide binding domains, NBD1 and NBD2, and the regulatory, R, domain.     

Studies on oligosaccharyl transferase in yeast

In yeast, OT consists of nine different subunits, all of which contain one or more predicted transmembrane segments. In yeast, five of these proteins are encoded by essential genes, Swp1p, Wbp1p, Ost2p, Ost1p and Stt3p. Four others are not essential Ost3p, Ost4p, Ost5p, Ost6p. All yeast OT subunits have been cloned and sequenced (Kelleher et al., 1992; 2003; Kelleher & Gilmore, 1997; Kumar et al., 1994; 1995; Breuer & Bause, 1995) and the structure of one of them, Ost4p, has been solved by NMR (Zubkov et al., 2004). Very recently, the preliminary crystal structure of the lumenal domain of an archaeal Stt3p homolog has been reported (Mayumi et al., 2007). Homologs of all OT subunits have been identified in higher eukaryotic organisms (Kelleher et al., 1992; 2003; Kumar et al., 1994; Kelleher & Gilmore, 1997).     

Role of ICAM-3 in Intercellular Adhesion and Activation of T Lymphocytes

The immune system requires a fine regulation of intercellular communication for its normal function. There are several regulated molecular pathways involved in leukocyte cell interactions (Springer, 1990; Hynes, 1992). Among them, the interaction of the leukocyte integrin LFA-1 (CDlla/CD18) with its ligands provides multiple accessory adhesion signals of capital importance during different functions of the immune response, such as antigen presentation (Harding and Unanue, 1991), T-B lymphocyte interaction (Moy and Brian, 1992), cellular cytotoxicity (Makgoba et al., 1988; Altmann et al., 1989; Davignon et al, 1981; Akella and Hall, 1992), allogenic and autologous mixed lymphocyte reactions (Bagnasco et al., 1990) and recirculation and homing of lymphocytes through tissue endothelium (Hamann et al., 1988; Pals et al, 1988).     

Role of ICAM-3 in Intercellular Adhesion and Activation of T Lymphocytes

The immune system requires a fine regulation of intercellular communication for its normal function. There are several regulated molecular pathways involved in leukocyte cell interactions (Springer, 1990; Hynes, 1992). Among them, the interaction of the leukocyte integrin LFA-1 (CDlla/CD18) with its ligands provides multiple accessory adhesion signals of capital importance during different functions of the immune response, such as antigen presentation (Harding and Unanue, 1991), T-B lymphocyte interaction (Moy and Brian, 1992), cellular cytotoxicity (Makgoba et al., 1988; Altmann et al., 1989; Davignon et al, 1981; Akella and Hall, 1992), allogenic and autologous mixed lymphocyte reactions (Bagnasco et al., 1990) and recirculation and homing of lymphocytes through tissue endothelium (Hamann et al., 1988; Pals et al, 1988).     

Diaphragms and flooding survival

Why don't the gas spaces of submerged organs of wetland plants flood extensively when damaged? In addressing this intriguing question, Soukup et al . (pp. 71–75 in this issue) report on the role of rhizome diaphragms as barriers to flooding in Phragmites australis . This should prompt some reappraisal of the ways in which flooding resistance can be realized, even perhaps in undamaged organs.
Most emergent wetland macrophytes have an abundance of interconnected internal gas space, much of it in the form of large voids transversely partitioned at intervals by perforated cellular plates termed diaphragms. Functionally, it provides a low-resistance pathway for internal oxygen transport to support the respiratory needs of submerged and buried organs (Armstrong, 1979; Armstrong et al ., 1988; Crawford, 1992) and facilitates carbon dioxide removal. However, it does more than this, since it enables oxygen to be released from the root to where it can support aerobic microbial activity in otherwise anaerobic sediments, and phytotoxin immobilization or destruction (Armstrong et al ., 1992; Begg et al ., 1994; Gilbert & Frenzel, 1998). This oxygen release is regarded by some as a valuable aid to effluent purification by constructed wetlands. Perhaps a less desirable property of this gas-space provision is its recently discovered role in enhancing the emissions of greenhouse gases such as methane from wetlands (Brix et al ., 1992; Chanton & Whiting, 1996; Crutzen, 1991; Dacey & Klug, 1979).     

RECENT ORNITHOLOGICAL PUBLICATIONS

Books: Andrews , I.J. 1995. The Birds of the Hashemite Kingdom of Jordan Barrows , E.M. 1995. Animal Behavior Desk Reference Briffett , C. & Supari , Sutari bin Catchpole , C.K. & Slater , P.J.B. 1995. Bird Song: Biological themes and variations Clement , P. 1994. The Chiffchaff Collar , N.J., Crosby , M.I. & Stattersfield , A.J. 1994. Birds to Watch 2: The world list of threatened birds Flade , M. 1994. Die Brutvogelgemeinschaften Mittel- und Nord-deutschlands Gehlbach . F.R. 1994. The Eastern Screech Owl: Life history, ecology and behavior in the suburbs and countryside Gill , F.B. 1995. Ornithology. 2nd edition Holz , R. 1994. Bibliographie ornithologischer Artikel aus Zeit-schriften und Periodika der DDR Hora , J., Kanuch , P. et al. 1992. Important Bird Areas in Europe Czechoslovakia Howell , S.N.G. & Webb , S. 1995. A Guide to the Birds of Mexia and Northern Central America Jackson , C. 1994. Bird Painting: The eighteenth century Krattiger , A.F., Mc Neely , J.A., Lesser , W.H., Miller , K.R., ST. Hill , Y. & Senanayake , R. (eds) Love , J.A. 1994. Penguins Reilly , P. 1994. Penguins of the World Lutwack , L. 1994. Birds in Literature Miller , R.I., ed. 1994, Mapping the Diversity of Nature Nechaev , V.A. 1995. Game- and Protected Birds of Sakhalin and the Kuril Islands (in Russian) Nettleship , D.N., Burger , J. & Gochfeld , M. 1994. Seabirds on Islands: Threats, case studies and action plans Olsen , K.M. & Larsson , H. 1995. Terns of Europe and North America Ridley . M. 1995. Animal Behavior Searcy , W.A. & Yasukawa , K. 1995. Polygyny and Sexual Selection in Red-winged Blackbirds Small , A. 1994. California Birds: Their status and distribution Summers , R.W. & Mc Adam , J.H. 1993. The Upland Goose: A study of the interaction between geese, sheep and man in the Falkland Islands Sutherland , W.J. & Hill , D.A. (eds). 1995. Managing Habitats for Conservation Walters , M. 1994. Birds' Eggs Wheeler , B.K. & Clark , W.S. 1995. A Photographic Guide to North American Raptors Also Received: Cabot , D. 1995. Irish Birds Chandler , D. & Langman , M. 1995. Bird Habitats and Conservation Chebez , J.C. & Bertonatti , C.C. 1994. La Avifauna de la Isla de los Estados, Mas de Aflo Nuevo y Mar circundante Tierra de Fuego, Argentina Dawson , L. & Langman , M. 1995. Bird Behaviour Dekker , R.W.R.J., Mc Gowan , P.J.K. & WPA/Birdlife /Species Survival Commission Megapode Specialist Group Granlund , J., Mc Peck , G.A. & Adams , R.J. 1995. The Birds of Michigan Geligan , J., Smith , M., Rogers , D. & Contreras , A. (eds). 1994 Green , I. & Moorhouse , N. 1995. A Birdwatchers' Guide to Turkey Hayman , P., Arlott , N. & Tarboton , W. 1994. Birds of Southern Africa: The SASOL Plates Collection Hustings , F. & van Dijk , K. 1994. Bird Census in the Kizilirmak Delta, Turkey, in Spring 1992 Inskipp , C. & Inskipp , T. 1994. An Introduction to Birdwatching in Bhutan Jenkins , D. (ed.). 1995. Proceedings of the 6th International Symposium on Grouse, 20–24 September 1993, Udine, Italy Kivit , H., Nijmeijer , H. & Ovaa , A. (eds). 1994. Wader and Waterfowl Migration in the Cukurova Deltas, South Turkey, Spring 1990 Kutac . E.A. & CARAN, C. 1994. Birds and Other Wildlife of South Central Texas: A handbook Monroe , B.L., JR. 1995. The Birds of Kentucky Noble , W.T. de (ed.). 1995. Birds of the Messolonghi Wetlands, Eastern Mediterranean Wader Project, Spring 1990 Olney , P.J.S., Ellis , P. & Fisken , F.A. (eds) Olsen , J. 1994. Some Time with Eagles and Falcons Palmer , M. 1994. A Birdwatching Guide to the Costa Blanca. Revised edition Piper , S.E. 1994. Mathematical Demography of the Cape Vulture Rogers , D.W. 1994. Site Guides: Costa Rica, a guide to the best birding locations. Pp. 90. McMinnville, Oregon: Cinclus Rogers , D.W. 1994. Site Guides: La Ruta Maya, a guide to the best birding locations of the Yucatan, Belize, Guatemala, Honduras and El Salvador Rogers , D.W. 1993. Site Guides: Venezuela, a guide to the best birding locations SKARPHÉØINSSON, K.H., PÉTURSSON. G. & HEMARSSON, J.Ó. 1994. Uatbreisla varpfugla à Suvesturlandi: Könnum 1987–1992 [Atlas of Breeding Birds in Southwestern Iceland: A survey 1987–19921 Speight , G. 1995. Finding Birds in Britain: A site guide Stone , C.J., et al. 1995. An Atlas of Seabird Distribution in Northwest European Waters Sueur , F. & Commecy , X. 1990. Guide des Oiseaux de la Baie de Somme Thomson , T. 1994. Birding in Ohio. 2nd edition Walters , M. 1995. The Pocket Guide to Birds of Britain and Europe Zink , G. & Bairletn , F. 1995. Der Zug europäischer Singvögel: Ein Atlas der Wiedefunde beringter Vögel     

Heat generation and dissipation in plants: can the alternative oxidative phosphorylation pathway serve a thermoregulatory role in plant tissues other than specialized organs?

A number of hypothetical physiological roles have been proposed for the cyanide-insensitive alternative pathway in plants (Palmer, 1976; Laties, 1982; Meeuse, 1984; Purvis and Shewfelt, 1994; Wagner and Krab, 1995). The calorimetric observations of Raskin and co-workers (Ordentlich et al., 1991; Nevo et al., 1992; Moynihan et al., 1995) are significant contributions showing an interesting metabolic, chilling-induced response of the alternative pathway activity and differences in the low-temperature response among species adapted to different climates. Since different oxidative pathways do not have large differences in enthalpy, and observed heat rate increases are insufficient to cause significant temperature increases of physiological importance in nonthermogenic plants, other explanations must be developed for the relationship between the partitioning of electron flow and physiological conditions such as low temperature. The induction and engagement of the alternative respiratory pathway is involved in metabolic stasis, maintaining proper balance between carbon flow, ATP-ADP ratio, and electron flow during fluctuating or extreme temperature conditions. The alternative oxidase is engaged when ATP requirements are adequately met, as discussed by Palmer (1976), Meeuse (1983), Lambers (1985), and Wagner and Krab (1995). The expression and kinetic activity of the alternative oxidase are regulated by concentrations of key metabolites (Day and Wiskich, 1995; Siedow and Umbach, 1995; Wagner and Krab, 1995; Day et al., 1996). Dynamic partitioning of electron flow between Cyt oxidase and the alternative oxidase depends on the kinetic behavior of the two oxidases and the substrate dehydrogenases (Day and Wiskich, 1995; Siedow and Umbach, 1995; Wagner and Krab, 1995; Day et al., 1996). Furthermore, Moynihan et al. (1995) found that Episces cupreata Hook, adapted to the tropics, has very little alternative oxidase activity compared with wheat (Nevo et al., 1992), adapted to a large range of temperature climates. This results is consistent with the general relation between the apparent alternative oxidase activity and the climate of origin of the species.     

Targeting of proteins into the peroxisomal matrix

Summary During the last few years much has been learned regarding signals that target proteins into peroxisomes. The emphasis in the near future will undoubtedly shift towards the elucidation of the mechanism of import. The use of mammalian and yeast cells deficient in peroxisome assembly and/or import (Zoeller & Raetz, 1986; Erdmann et al., 1989; Cregg et al., 1990; Morand et al., 1990; Tsukamoto, Yokota & Fujiki, 1990) should provide a handle on the genes (Erdmann et al., 1991; Tsukamoto et al., 1991) involved in these processes. This will have to be coupled with further development of in vitro systems which will permit the dissection of the steps in the translocation of proteins into peroxisomes. Though some progress has been made in the development of such assays (Imanaka et al., 1987; Small et al., 1987, 1988; Miyazawa et al., 1989), the fragility of peroxisomes and the absence of biochemical hallmarks of import (such as protein modifications or proteolytic processing) have hindered progress. Since peroxisomes exist in the form of a reticulum in mammalian cells (Gorgas, 1984), all peroxisome purification schemes (from mammalian cells at least) must undoubtedly rupture the peroxisomes, which then reseal to form vesicular structures. Additionally, the reliance on the latency of catalase alone as a major criterion for the integrity of peroxisomes ignores the fact that many other matrix proteins leak out of peroxisomes at vastly different rates during purification of the organelles (Thompson & Krisans, 1990). In view of these problems, the development of peroxisomal transport assays with semi-intact cells would also constitute an important advance. It is very likely that in the next few years we will witness some major advances in our understanding of the mechanism by which proteins enter this organelle.I would like to thank all the members of my lab and my collaborators, past and present, whose hard work provided the material for this review. This work has been supported by grants from the March of Dimes Foundation (#1081) and the NIH (DK41737).     

Cellular Redistribution of Protein Tyrosine Phosphatases LAR and PTPσ by Inducible Proteolytic Processing

Most receptor-like protein tyrosine phosphatases (PTPases) display a high degree of homology with cell adhesion molecules in their extracellular domains. We studied the functional significance of processing for the receptor-like PTPases LAR and PTPσ. PTPσ biosynthesis and intracellular processing resembled that of the related PTPase LAR and was expressed on the cell surface as a two-subunit complex. Both LAR and PTPσ underwent further proteolytical processing upon treatment of cells with either calcium ionophore A23187 or phorbol ester TPA. Induction of LAR processing by TPA in 293 cells did require overexpression of PKCα. Induced proteolysis resulted in shedding of the extracellular domains of both PTPases. This was in agreement with the identification of a specific PTPσ cleavage site between amino acids Pro₈₂₁ and Ile₈₂₂. Confocal microscopy studies identified adherens junctions and desmosomes as the preferential subcellular localization for both PTPases matching that of plakoglobin. Consistent with this observation, we found direct association of plakoglobin and β-catenin with the intracellular domain of LAR in vitro. Taken together, these data suggested an involvement of LAR and PTPσ in the regulation of cell contacts in concert with cell adhesion molecules of the cadherin/catenin family. After processing and shedding of the extracellular domain, the catalytically active intracellular portions of both PTPases were internalized and redistributed away from the sites of cell–cell contact, suggesting a mechanism that regulates the activity and target specificity of these PTPases. Calcium withdrawal, which led to cell contact disruption, also resulted in internalization but was not associated with prior proteolytic cleavage and shedding of the extracellular domain. We conclude that the subcellular localization of LAR and PTPσ is regulated by at least two independent mechanisms, one of which requires the presence of their extracellular domains and one of which involves the presence of intact cell–cell contacts. A key element in the regulation of cell–cell and cell– matrix contacts is the tyrosine phosphorylation of proteins that are localized in focal adhesions and at intercellular junctions (for reviews see Kemler, 1993; Clark and Brugge, 1995). While much is known about the protein tyrosine kinases involved in the phosphorylation of cell adhesion components, very little information exists about the identity of protein tyrosine phosphatases (PTPases),¹ which are responsible for the dephosphorylation and thereby regulation of these structural complexes. Probable candidates are those receptor-like PTPases that contain cell adhesion molecule-like extracellular domains and could therefore regulate their intrinsic phosphatase activity in response to cell contact. Recent reports suggest that some PTPases do, in fact, possess properties that resemble those of classical cell adhesion molecules (for review see Brady-Kalnay and Tonks, 1995). A direct involvement in cell–cell contact has so far been demonstrated for PTPμ (Brady-Kalnay et al., 1993; Gebbink et al., 1993) and PTPκ (Sap et al., 1994), for which a homophilic interaction between their extracellular domains was found. The localization of PTPμ (Brady-Kalnay et al., 1995; Gebbink et al., 1995), PTPκ (Fuchs et al., 1996), and PCP-2 (Wang et al., 1996) was restricted to sites of cell–cell contact and surface expression of PTPμ (Gebbink et al., 1995), and PTPκ (Fuchs et al., 1996) was increased in a cell density-dependent manner. Moreover, a direct association of PTPκ (Fuchs et al., 1996) and PTPμ (Brady-Kalnay et al., 1995) with members of the cadherin/catenin family suggests that proteins of the cell adhesion complex represent physiological substrates for these PTPases. A possible regulatory function in cell–matrix adhesion has been proposed for LAR, another receptor-like PTPase, which associated with focal cell–substratum adhesions via the newly identified LAR interacting protein 1, LIP-1 (Serra-Pages et al., 1995).PTPμ (Gebbink et al., 1991), PTPκ (Jiang et al., 1993; Fuchs et al., 1996), PTPδ (Krueger et al., 1990; Mizuno et al., 1993, Pulido et al., 1995a), PCP-2 (Wang et al., 1996), and LAR (Streuli et al., 1988, Pot et al., 1991) are members of the so-called type II receptor-like PTPases. The extracellular domains of these PTPases contain a variable number of Ig-like and fibronectin type III-like (FNIII) domains (for review see Charbonneau and Tonks, 1992). With the exception of PCP-2 (Wang et al., 1996), these PTPases also share characteristics in their biosynthesis. They all underwent proteolytic processing by a furin-like endoprotease and were expressed at the cell surface in two subunits which were not covalently linked (Streuli et al., 1992; Yu et al., 1992; Jiang et al., 1993; Brady-Kalnay and Tonks, 1994; Gebbink et al., 1995; Pulido et al., 1995a; Fuchs et al., 1996). It was shown for LAR that the E subunit, which contains the cell adhesion molecule-like extracellular domain, was shed from the cell surface when cells were grown to a high density (Streuli et al., 1992). This shedding of the E subunit of LAR was the result of an additional proteolytic processing step that could also be induced by treatment of the cells with the phorbol ester TPA (Serra-Pages et al., 1995). An accumulation of E subunits in the supernatant of cells was also observed for PTPμ (Gebbink et al., 1995) and PTPδ (Pulido et al., 1995a), and this suggests a common mechanism in the regulation of type II PTPases. However, the effect of proteolytic processing on either the catalytic activity, the substrate specificity, or the cellular localization of these PTPases has not yet been determined. We report here that PTPσ, a recently identified new member of the family of receptor-like type II PTPases (Pan et al., 1993; Walton et al., 1993; Yan et al., 1993; Ogata et al., 1994; Zhang et al., 1994), underwent biosynthesis and proteolytic processing in a manner that resembled that of the most closely related PTPase LAR. Moreover, further proteolytic processing of PTPσ as well as of LAR could be induced by treatment of the cells with TPA or the calcium ionophore A23187. Transient expression studies indicated that TPA-induced processing of LAR, but not PTPσ, was dependent on the coexpression of PKCα. Inducible processing of both PTPases took place in the extracellular segment of the P subunit in a juxtamembrane position and led to the shedding of the E subunit. Both LAR and PTPσ were predominantly localized in regions of cell–cell contact and accumulated in dot-like structures that could be identified as adherens junctions and desmosomes by colocalization with plakoglobin (Cowin et al., 1986). Moreover, plakoglobin and β-catenin, another component of E-cadherin–containing cell adhesion complexes in adherens junctions, associated directly with the intracellular domain of LAR in vitro. The inducible shedding of the E subunit of LAR and PTPσ was followed by a redistribution of the PTPases within the cell membrane and by an internalization of the cleaved P subunits. It therefore represents a mechanism through which the phosphatase activity of these PTPases could be regulated in response to cell–cell contact. The cell adhesion molecule-like character of LAR and PTPσ was further supported by the fact that the internalization of LAR and PTPσ occurred independently of the proteolytic processing if cells were grown in calcium-depleted growth medium. The analogies in specific localization as well as internalization behavior of PTPσ and LAR, with molecules of the cadherin/catenin family, strongly suggest a direct involvement of PTPσ and LAR in the formation or maintenance of intercellular contacts.     

Major Biological Issues Resulting from Anthropogenic Disturbance of the Nitrogen Cycle

A two-day Discussion Meeting of the Royal Society, 'The Nitrogen Cycle', held in London in June 1991 (Stewart & Rosswall, 1992) reviewed the considerable progress made in understanding the N cycle in agricultural, forest and aquatic systems. The meeting included some discussion of the concerns which were already being expressed at that time over nitrate in water supplies, and the impacts of nitrogenous gases on tropospheric chemistry, the greenhouse effect and the ozone layer. Since then, disquiet over the impacts of nitrogenous compounds on the environment has increased, and numerous papers have been published on many aspects of the problem. We now have much better understanding of the size and scale of the perturbation of the N cycle, and several review papers have highlighted the complexity of the formidable issues that are challenging environmental scientists (Vitousek, 1994; Galloway et al ., 1995; Vitousek et al ., 1997).     

Haemophilus somnus - Unlikely to be a Causative Microbiological Agent in Bovine Clinical Mastitis in Denmark

Haemophilus somnus is a Gram-negative bacterium, which is the cause of a clinical syndrome in cattle that may include pneumonia, myocardial abscessation, arthritis, thrombotic menin-goencephalitis, genital infections and mastitis (Humphrey & Stephens 1983, Armstrong et al. 1986, Higgins et al. 1987, Harris & Janzen 1989, Kwiecien & Little 1992). In Denmark the infection is mainly found in the respiratory tract of calves (Krogh et al. 1986, Wedderkopp 1991).